Morgellons : Unique Protein Isolated & Characterized


Unique Protein Isolated & Characterized

Clifford E Carnicom
Aug 13 2017
 Note: Carnicom Institute is not offering any medical advice or diagnosis with the presentation of this information. CI is acting solely as an independent research entity that is providing the results of extended observation and analysis of unusual biological conditions that are evident.  Each individual must work with their own health professional to establish any appropriate course of action and any health related comments in this paper are solely for informational purposes.


A protein generated by the microorganism associated with the Morgellons condition (tentatively classified in past research as a “cross-domain bacteria”, i.e., CDB) has been isolated and characterized in several ways.  There is little doubt that this protein is at the heart of the physiological and biochemical changes that occur within the body by those affected.  Related research has been conducted with success for some time, however, the recent work represents a different and separate approach from previous accomplishments.  Proteins are at the crux of biochemistry and biological research, and they have great importance within any of the structural forms of life.  There are usually numerous applications (beyond health aspects alone) that develop with the advent of a new or isolated protein, and it is expected that the current work can eventually follow this suit.

Only the general nature of the protein will be described at this point.  The protein is organometallic in nature, highly water soluble, and strongly acidic.  Additional resources of significance and support from the health communities will be required to develop the series of discoveries into tangible benefits.

Some of the methods that been employed to define the unique nature and characteristics of the protein include:

  1. The molecular weight of the protein has been estimated with laboratory methods.
  2. The solubility and polarity of the protein has been assessed.
  3. Pyrolysis with gas chromatography (GC) has been applied to the protein to examine its thermal decomposition into various subcomponents.
  4. Headspace methods have been used to examine the nature and volatility of gaseous metabolism of the microorganism.
  5. Infrared (IR) analysis has been used to identify the primary functional groups of the protein, along with the analysis of various GC trapped components.
  6. Ultraviolet (UV) analysis of the protein has been conducted.
  7. Candidate amino acid composition, at least to a partial extent, has been established.
  8. The pH of the protein has been measured.
  9. The isolectric point of the protein has been determined via titration.
  10. Precipitation methods for the protein have been developed.
  11. A metallic nature of the protein has been verified.
  12. The index of refraction for the protein has been determined by measurement.
  13. A concentration-dilution model for the protein has been developed based upon the index of refraction.
  14. The polarimetric nature of the protein has been examined.
  15. A colorimetric test for the existence of the protein has been established.
  16. Initial molecular models proposals have been established for some of the simpler components of the headspace-pyrolysis components with GC – IR coupling.
  17. Initial anticipated impacts upon physiology, i.e., absorption levels, are under investigation.

GC Pyrolysis Chromatogram of Numerous Components of CDB Isolated Protein
(significant hydrocarbon structure is identified within)


The isolation and characterization of this particular protein and its properties are of importance and uniqueness in the research related to the Morgellons condition. The attributes identified are numerous and specific to the microorganism that has been extensively identified, examined and researched.  The uniqueness of the protein is essentially guaranteed.  The method of development of the protein also represents a distinct and recent advance in the history of CI research, and it is hoped at some point that the work will be placed to the advantage and benefit of the public.


Clifford E Carnicom
Aug 11 2017

Born Clifford Bruce Stewart
Jan 19 1953



Carpinteria Crystal

Carpinteria Crystal

Clifford E Carnicom
Sep 25 2016

An environmental crystal sample sent to Carnicom Institute from a concerned citizen has been analyzed as to its nature.  The ground sample was received three years ago and it has been held in custody since that time.  Circumstances are now more favorable toward establishing the identity or nature of inorganic compounds, and thus the opportunity to do so in this case has been exercised.  The sample originates from the Santa Barbara – Carpinteria region of the country.  The sample is well documented, clean, and has been collected and transported in a careful fashion.

One of the reasons for the interest in the sample is a repetition of events.  The citizen reports that similar appearing materials  have occurred within the same coastal housing district on multiple occasions over a period of many years.  In addition, the findings of this study may have relevance to a paper presented earlier on this site.  The interest in devoting time to sample analysis is directly related to the the frequency and pattern of appearance.

There are also several occasions of crystal samples collected or received over the years that have not received proper attention due to insufficient resources and means for investigation.  The majority of these cases, to my recollection, resulted from air filtration systems.  These deficiencies have likely delayed our understanding of various forms of pollution that likely surround us, and this will remain the case until full and sufficient resources are devoted to these types of problems.  It is the opinion of this researcher that the regulating environmental protections agencies have an obligation to this end and that it has not been well served.

This particular sample has the following appearance:


Environmental Crystal Sample Material Received in 2013


The purpose of this paper is not to debate the origin or delivery method of the sample; the information available is insufficient to fully detail those answers.  It can be stated in fairness that the observer witnessed heavy aerosol  operations over the region in the early hours of the day of collection of the sample.  The density and activity level of the operations was stated to be high.

The purpose of this paper IS to call attention to what may be a repeating type of material that has potentially important environmental consequences, particularly if they are found to exist in aerosol or particulate form within the general atmosphere.  The sample type is also fully consistent with many of the analyses and postulates that have developed within the research over the years.  The specifics of that discussion will follow within this paper.

The sample has been evaluated using multiple approaches.  These include, but are not limited to:

  1. Electrochemistry techniques, specifically differential normal pulse voltammetry.
  2. Solubility analyses
  3. Melting point determination
  4. Density estimates
  5. Microscopic crystal analysis
  6. Qualitative reagent tests
  7. Conductivity measurements
  8. Index of refraction measurements

The results of these analyses indicate that the dominant component of the material is that of potassium chloride, a metallic salt form.  There are indications that the sample does contain more than one component, but any further investigation will have to take place at a later time.   Every physical and chemical form has implications, applications and consequences, especially if they occur in a manner foreign or unexplained to the environment.  The material shown above is of no exception to those concerns.  It may be the case that the appearance of this material in an unexplained manner and location is of no consequence; prudence, however, would suggest that we are obligated to seek out that which has no accountable explanation.  This premise is at the very heart of any forensic investigation, and environmental science and pollution control are also subject to that very same demand.



A brief bit of historical perspective on this topic could be helpful.  A search on this site on the subject of crystals will bring up a minimum of eight additional papers that are relevant; there are likely to be more.  These papers range in date from 2001 to the current date, so from this standpoint alone there is a repeating issue involved here.

A search on this site for historical presentation on potassium issues produces at least three papers on the subject.  There is reason to consider, therefore, that potassium (and related) chemical compounds may be worthy of examination with respect to geoengineering as well as biological issues.

Within this combined set of close to a dozen or more papers on the subjects, two will be mentioned further at this time.

The first will be that of another sample, also of a crystalline nature, received in 2003 from the same specific region of the country.  The title of that short report is “Additional Crystal Under Examination” (Jun 2003).  There are three points of interest in comparison between that and the current report:

1. Two generally similar and unaccountable sample forms appear in similar locations over a 10 year period, and a public interest in identification of the nature of the material remains over this same prolonged period.

2. The report in 2003 is reasonably brief with a limited microscopic examination offered.  The topic is mentioned more in the sense of an anomaly and a curiosity as there is no basis at the time for an in depth study of the materials; in addition, resources to do so at the time are non-existent.

3. The third will be the comment regarding the lack of water solubility of the first sample.  The importance of this observation will be the fact that the samples, although visually similar, have important differing chemical properties.  The conclusion is that multiple material types are expected to be subject to investigation over the course of time.

The second will be that of a laboratory report received in the year of  2005.  The title of that paper is “Calcium and Potassium” (Mar. 2005).  The importance and relevance of this paper can be understood from the opening paragraph:

A laboratory analysis of a rainwater sample from a rural location in the midwestern U.S. has been received.  This lab report reveals extremely high levels of potassium and calcium within the sample. Comparative studies have been done and they show that the calcium concentration is a minimum of 5 times greater, and that the potassium level is a minimum of 15 times greater than that which has been reported1 in the polluted skies of Los Angeles, California.

It will also be noticed that several health and environmental concerns with respect to aerosolized potassium salts are enumerated in that latter paper.  Attention should also be paid to the intriguing discussion of electromagnetic effects and impacts that must be considered with the chemistry of potassium and related ions.

Potassium chloride has common uses as well, such as a fertilizer or as a water treatment compound; there is, however, no cause given to think that it is being used in such fashions at this location and setting at this time.



Let us now bring ourselves back to the current moment.  The relevance and direction of those papers have borne themselves out over time, and the urgency of responsibility upon us is as imposing as ever.  We do not have the luxury of another 20 years to conclude on such an obvious state of affairs.

There are at least three immediate applications or consequences of the existence of aerosolized potassium chloride upon the atmosphere that should be mentioned.

1. Heat Impacts

2. Moisture Impacts

3. Electromagnetic Impacts

With respect to heat impact, potassium chloride is highly soluble within water.  When it does dissolve, it absorbs heat from the water, and the magnitude is significant.  Potassium chloride has actually been used as a cold pack commercially for this same reason; it is also readily available and relatively inexpensive.  It therefore can potentially be used to influence atmospheric thermodynamics, and this is one of many leads of investigation to pursue.

On the flip side of the equation, potassium chloride in a solid state has a rather low specific heat, especially relative to that of both air and water.  This means that, depending upon the state of the surrounding atmosphere, that it can also possess the capability to heat the atmosphere, rather than to cool it.

Furthermore, potassium as a metal in its elemental form also has a lower specific heat than air and once again this may allow for a net heating impact upon the atmosphere, depending on states of being, location and interaction with other elements or compounds.

The point of this discussion is that metallic salts of any kind DO have an impact upon the heating dynamics of the atmosphere, and that this process can be both complicated and variable.  You cannot place anything into the atmosphere without having an effect in some fashion, and it is a mistake to oversimplify and overgeneralize as to what those changes will be.  The location of placement of aerosols is another matter also, as has been discussed extensively on this site.

We are, therefore, not permitted to remain ignorant of the impacts that foreign and contaminating materials have upon the environment; heat dynamics are only one of many aspects of that we are forced to confront when the atmosphere is altered in ANY significant fashion.

There are, of course, many other environmental consequences from the addition of ionizable metallic salts into the environment.  These include plant life and agriculture, for example.  Readers may also wish to become familiar with a discussion regarding soil impacts as presented within the paper “The Salts of Our Soils” (May 2005).

As far as moisture is concerned, heat and moisture are obviously very closely related subjects.  One of the trademarks of the salt genre is that of absorbing moisture.  Some salts attract moisture so strongly that they are hygroscopic, meaning that they can draw moisture from the ambient atmosphere.  The observation of this phenomenon is quite remarkable; one can start with a solid and watch it change to an eventual liquid form.  Calcium chloride and strontium chloride are both good examples of this class of materials.

Locking moisture up in this fashion will most certainly increase the heat in the atmosphere; water is one of the greatest cooling compounds that exists on the planet.  It is impossible to separate heat and moisture impacts when dealing with aerosolized metallic salts; it is certain that there will be an impact upon the atmosphere,  environment and health.  It is difficult to predict a favorable outcome here.

Lastly, there may still be some that will ridicule the notion of electromagnetic impacts of ionized metallic salts upon the atmosphere and the environment.  I think such an approach might ultimately be foolhardy.  This tenet was brought forth early in the research of this organization, and the premise remains as strong as when it is originated.  For those that care to repeat the enterprise, there are measurements to support the hypothesis, and they only continue to accumulate.

For those that seek conventional sources, one need look no further than a document that traces back to the 1990’s, entitled “Modeling of Positively Charged Aerosols in the Polar Summer Mesopause Region” (Rapp, Earth Planets Space 1999).  A very specific reference of the ability of potassium in combination with ultraviolet light to increase the electron density of the atmosphere will be found there.  There are other elements that share in this remarkable physical property, and they have been discussed within this site for many years now.  Reading the patents by Bernard Eastlund may also be insightful.  The ability of moisture to ionize many metallic salts is also to be included within the examinations that are required to take place.

It is difficult to ignore and discount the fundamental heat, moisture, and electromagnetic impacts upon the planet when metallic salts are artificially introduced into the atmosphere.  It would not be wise to do so.  The case for investigation, accountability and redress is now strong, and each of us can make the choice as to how to best proceed.  It seems to be a simple matter to want to protect and ensure the welfare of our gifted home, as our existence depends upon it.  Clarity and unity of purpose would seem to be an end goal here; I hope that each of us will seek it.

Regardless of the origin of this particular sample (which is unlikely to ever be known exactly), this report points to the requirement of identifying repetitive and unknown contaminants in the environment.  The responsibility for this process does not fall either primarily or exclusively upon the citizens; this population has neither the resources or means to perform or satisfy the requirements of identification, evaluation and assessment.  Entrusted agencies that exist specifically for protection of the welfare of the common environment (e.g., air, water, soil) and that are funded by these same citizens ARE required to do so.  In this vein, I will once again repeat the closing statement from above:

Clarity and unity of purpose would seem to be an end goal here; I hope that each of us will seek it.


Clifford E Carnicom

Sep 25 2016


Supplemental Discussion:

Approximately a dozen methods of investigation have been used to reach the conclusions of this report.  These will now be described to a modest level of detail to assist in portraying the complexities of analyzing unknown environmental samples.  This description will further the argument that the citizenry is not realistically expected to assume this burden and cost; contamination and pollution are at the heart of existence for publicly funded environmental protection agencies and entities.  It is recommended that the public seek the level of accountability that is required to reduce and eliminate persistent and harmful pollution and the contamination of our common environment.

1. Voltammetry:

The methods of differential pulse voltammetry have been applied to the sample.  The methods are quite useful in the detection of inorganics, especially metals and trace metal concentrations.  The results of the analysis are shown below:


Differential Normal Pulse Voltammetry Analysis of Crystal Sample

The analysis indicates a minimum of two chemical species to consider.  The first of these is a suspected Group I or Group II element (-2.87V).  The most probable candidates to consider will be that of calcium, strontium, barium and potassium.  The other will be the consideration of  the chloride ion ( +0.63V and +1.23V).

At this point of the investigation, our strongest prospect will therefore be an ionic metallic salt crystalline form, most likely involving a subset of Group I or II of the periodic table.  The most likely candidate will, furthermore, be a chloride form of the salt.

2. We can then proceed to solubility tests.  Four candidates from above will now be considered, along with two additional candidates resulting from the chloride prospects:

calcium chloride
strontium chloride
barium chloride
potassium chloride

lithium chloride
cesium chloride

With respect to the first set of four, the solubility tests applied (i.e., water, methanol, acetone, sodium bicarbonate, acid, base) eliminate all but potassium chloride for further examination.

This reduces the primary set of consideration to that of:

potassium chloride
lithium chloride
cesium chloride

We now attempt to confirm the existence of the chloride ion in a redundant fashion.  A qualitative chemical test (HCl, AgNO3) is then applied to the sample in aqueous solution.  The existence of the chloride ion is confirmed.  The set of three candidates remains in place.

The next method applied to the sample is the determination of the melting point of the presumed ionic crystal form.  Ionic metallic salts have generally high melting points and this does present some difficulties with the use of conventional equipment and means.

The methods of calorimetry were adapted to solve this particular problem.  The methods were also applied to a control sample of potassium chloride, as well as two additional control compounds.  The results of the control and calibration trials produced results within the range of expected error (~ < 5%).

The melting point of the crystal form was determined experimentally by the above methods as approximately 780 deg. C.  The melting point of potassium chloride is 770 deg. C.  This result is well within the range of expected experimental error (1.4%).  During the process, it was noticed that an additional minority compound does exist within the sample, as a small portion of the sample does melt at a much lower point (est. 300-400 deg. C.) The minority compound would require separation and identification in a further analysis.

The melting points of lithium chloride and cesium chloride are 605 deg. C. and 645 deg. C., respectively, and they are thus eliminated from further consideration.

These results narrow the list of candidates specifically to that of potassium chloride.

An additional controlled test of conductivity of the salt in solution was applied.   The result of that test indicates agreement in conductivity with a known concentration solution of potassium chloride.  The error in that case was also well within the expected range of experimental error (0.6%).

In addition, further tests involving density determination, index of refraction, visual and microscopic crystal analysis further substantiate the identification of the crystal as being primarily that of potassium chloride.

The Demise of Rainwater

The Demise of Rainwater

Clifford E Carnicom

A Paper to be Developed During
the Summer of 2016
(Last Edit Jun 20 2016)

The single most important chemical species in clouds and precipitation is the .. pH value.

Paul Crutzen, Nobel Prize Winner in Chemistry, 1995

Atmosphere, Climate and Change, Thomas Graedel & Paul J. Crutzen

Scientific American Library, 1997


Photo : Carnicom Institute

An analysis of five rainfall samples collected over a period of six months and spanning three states in the western United States has been completed.  There are five conclusions that are forthcoming:

1. The rainfall samples studied portray a smorgasbord of contamination. The contaminants appear to be both complex and numerous in nature.

2. There does not appear to be effective or comprehensive monitoring or regulation of the state of air quality, and consequently, rainfall quality in the United States at this time.

3. The results of the current analysis, utilizing more capable equipment and methods, are highly consistent with those that originated from this researcher close to two decades ago.

4. All reasonable requests or demands by the citizenry for the investigation and addressing of this state of affairs over this same time period have been refused or denied.

5. The level of contamination that exists poses both a risk and a threat to health, agriculture, biology, and the welfare of the planet.


Let us now proceed with some of the details.

We can begin with the pH, i.e., the acid or alkaline nature of rainfall.  Biochemical reactions take place (or, for that matter, do not take place..) at a specific temperature and pH.  If the system or environment for that reaction is disturbed with respect to the acidity and temperature, then the reaction itself is interfered with.  If the conditions depart far enough from what is required, the reaction may simply not even take place at all.  Such is the risk of interference to the acid-base nature of rainfall, upon which all life on this planet depends.


To be continued.





UV Detector & Lab Equipment Used for Summary View Data


Rainfall Analysis_16

Electrochemical Signature of Rainwater Tests for Trace Metals
as Determined by Differential Normal Pulse Voltammetry

The following metallic elements have been determined to exist, or to be strong candidates to exist, within a series of five rainwater samples that have been tested for trace metals.  The samples span three states across the country and six months of time.  The method applied is that of Differential Normal Pulse Voltammetry.  The level of detection for the method is on the order of parts per million (PPM).  This list considerably extends the scope of consideration for the future investigation and detection of metallic elements within rainwater.  The findings in the upper portion of the table are highly consistent with those under reporting by various laboratories across the country; those in the lower half serve to prompt further investigations into additional elements that are highly related in their properties within the periodic table.  An examination of the physical properties of these elements, in detail, will likely provide additional insight into the applications of use for these same elements.  It can be noticed that the majority of elements within the list act as reducing agents.

Element Measured Mean Redox Voltage
(Absolute Value)
Actual Redox Voltage
(Absolute Value)
Titanium (Ti) 1.63, 1.32, 1.24 1.63, 1.31, 1.23
Aluminum (Al) 1.67 1.66
Barium (Ba) 2.90 2.90
Strontium (Sr) 2.90 2.89
Magnesium (Mg) 2.66, 2.35 2.68, 2.37
Gallium (Ga) .52, .65 .56, .65
Scandium (Sc) 2.56, 2.09 2.60, 2.08
Zirconium (Zr) 1.45 1.43
Standard Error of Measurement 0.013 V; n = 15
(No information regarding concentration or concentration ranking is provided here)


Additional Inorganic Analyses:

Qualitative (Color Reagents) Test Results for Combined Rainfall Sample
A Value of 1 Indicates a Positive Test Result
Concentration of RainwaterSample ~15x
(No information regarding concentration or concentration ranking is provided here.)
(Chromium, Cyanide & Iron appear to be at minimal trace levels)


Qualitative Positive Test Examples:
Phosphates, Nitrates, Ammonia, Silica




Tests to Determine the Boiling Point
for the Concentrate Rainfall Sample Using an Oil Bath
(Contamination is Evident)





An Organic Extraction Process

(Results subsequently to be examined by Infrared Spectroscopy)


Infrared Spectrum of Rainfall Organic Extraction :

Water Soluble & Insoluble Components

(see previous photo)

(solvent influences removed)


Gas Chromatography (TCD) Applied to Organic Extracts

(tailing from varying polarities)




Biologicals Extracted from Rainfall Concentrate Samples


Additional Note:

I wish to thank Mr. John Whyte for his dedication and effort to organize and produce an environmental conference in Los Angeles, California during the summer of 2012. Mr. Whyte, in support of the speakers at the conference, provided the means for some of the environmental test equipment used in this report. I also wish to thank the general public for their assistance during this last year in the acquisition of important scientific instrumentation by Carnicom Institute. This report is made possible only by that generosity.

Clifford E Carnicom

Jun 18, 2016

To be continued.

Tertiary Rainwater Analysis : Questions of Toxicity

Tertiary Rainwater Analysis : Questions of Toxicity

 Clifford E Carnicom
Nov 08 2015


This paper presents evidence of a chemical signature that exists within an analyzed rain sample that is characteristic of known toxins and pesticides. The method of analysis used is that of mid-infrared spectroscopy. Specifically, certain functional groups involving sulfur, nitrogen, phosphorus, oxygen, and halogens have been identified in the analysis. It is recommended that the investigation be duplicated by independent researchers to determine if an environmental hazard does exist. If these results are verified to be positive, the source of the contaminants is to be identified and eliminated from the environment.

residual_ir4Infrared Spectrum of Concentrated Rain Water Sample
(Aqueous Influence Removed)

The original rainwater sample volume for this analysis is approximately 3.25 liters.  The sample was evaporated under mild heat to approximately 0.5% of the original volume, or about 15 milliliters.  The sample has previously been shown to contain both aluminum, biological components, and a residue that appears to be an insoluble metallic or organometallic complex.  The target of this particular study is that of soluble organics.

The organic infrared signal within the solution is weak and difficult to detect with the means available; it is further complicated by being present in aqueous solution.  The aqueous influence was minimized by making an evaporated film layer on a KCl cell; the transmission mode was used. The signal is identifiable and repeatable under numerous passes in comparison to the reference background.

The primary conclusion from the infrared analysis is that a core group of elements exists within the solution; these appear to include carbon, hydrogen, nitrogen, sulfur, phosphorus, oxygen and a halogen.  The organic footprint appears to be weak but detectable and dominated by the above heteratoms.

As further evidence for the basis of this report, qualitative tests for an amine (nitrogen and hydrogen), sulfates and phosphates (sulfur, oxygen and phosphorus) have each produced a positive test result.  A qualitative test for a halogen in the concentrated rainwater sample has also produced a positive result; the most likely candidate at this point is the chloride ion.  All elements present have therefore been proven to exist at detectable levels by two independent methods.

This grouping of elements is distinctive; they essentially comprise the core elements of many important, powerful and highly toxic pesticides.   For example, three sources directly state the importance of the group above as the very base of most pesticides:


“In pesticides, the most common elements are carbon, hydrogen, oxygen, nitrogen, phosphorus, sulfur and chlorine”.

Pesticide Residues in Food and Drinking Water : Human Exposure and Risks, Dennis Hamilton, 2004.


“We can further reduce the list by considering those used most frequently in pesticides: carbon, hydrogen, oxygen, nitrogen, phosphorus, chlorine, and sulfur”.

Fundamentals of Pesticides, A Self-Instruction Guide, George Ware , 1982.


“Heteratoms like fluorine, chlorine, bromine, nitrogen, sulfur and phosphorus, which are important elements in pesticide residue analysis, are of major interest”.

Analysis of Pesticides in Ground and Surface Water II : Latest Developments, Edited by H.J. Stan, 1995.


It is also true that phosphate diesters are at the core of DNA structure and that many genetic engineering procedures involve the splitting of the phosphate diester complex.

The information provided above is sufficient to justify and invoke further investigation into the matter.  The sample size, although it was derived from an extensive storm over several days in the northwest U.S., is nevertheless limited and quite finite after reduction of the sample volume.  The residual insoluble components (apparently metallic in nature) are also limited in amount and more materials will be required for further analysis.  The signal is weak and difficult to isolate from the background reference; concentration level estimates for elements or compounds (other than that of aluminum which has been assessed earlier) is another entire endeavor.  Systematic, wide-area, and long term testing will be required to validate or refute the results.  All caveats above aside, it would seem that the duty to address even the prospect of the existence of such toxins in the general rainfall befalls each of us.  It would seem wise that this process begins without delay.

There are a few additional comments on this finding that need be mentioned.

The first of these is the issue of local and regional vs. a national and international scope of consideration.  It is understood that pesticides or compounds similar in nature are a fact of our environment, and that considerable awareness and effort is in place to mitigate their damage over decades of use.  Organic farming and genetically engineered crops are two very divergent approaches to reconciliation with the impact of environmental harm, and they are shaping our society and food supply in the most important ways manageable.  Given that the pesticide industry exists, regardless of our varying opinions of merit or harm, I think that it is fair to say that we generally presume that pesticides are under some form of local control.  Our general understanding is that pesticides are applied at ground or close to ground level and are intended to be applied to a specific location or, at most, a region within a defined time interval.

The prospect, even I daresay, the hint, of pesticide or pesticide-like compounds in rainfall is more than daunting.  It seems immediately necessary to consider what scale of operation would support such toxins finding their way into the expanses of atmosphere and rainfall?  For the sake of the general welfare, I think we should all actively wish and seek to disprove the findings within this report.  I will not hesitate to amend this report if honest, fair and accurate testing bears out negative reports over an adequate time period, and my motive never includes sensationalizing an issue.  This is one test, one time, one place, with limited means and support in the process.  I cannot disprove the results at this time and I have an obligation to report on that which seems to be case, uncomfortable as it might be.  It is not the first time that I have been in this situation, and judging from the changes in the the health of the planet that have taken place, it is unlikely to be the last.  The sooner that the state of truth is reached, the better we shall all be for it in any sense that is real.

The second comment relates to the decline of the bee population.  Bees are an indicator species, the canary in the mine, as it were.  The bees and the amphibians have both been ringing their alarm for some time now, and we best not remain passive about finding the reasons for decline.  A minimum of 1/3 of our agricultural economy, and that means food, is dependent upon the bee population for its very existence.  This is no trifling matter, and we all need to get up to speed quickly on the importance of this issue, myself included.

Suffice it to say that compounds of this nature, i.e, historical pesticides like organophosphates and the purported safer and more recent alternatives (e.g., the neonicotinoids), have a very close relationship to the ongoing and often ambiguous studies regarding bee Colony Collapse Disorder (CCD).  From my perspective, it would seem prudent to eliminate the findings of this report as a contributing cause to the problem as promptly as possible.  If that can not be done so readily, then we may have a bigger problem on our hands than is imagined.

One of the interesting side notes is that the elements and groups identified as candidates for investigation actually seem to overlap between the neonicotinioids and the organophosphates.  This includes the nitrogen groups that characterize the neonicotinoids and the phosphate esters that characterize the organophosphates.  If such a combination were at hand, this would seem especially troublesome as both forms remain mired in controversy, let alone any combination thereof.

The third and final comment relates to the toxicity of these compound types in general.  It is not just an issue about bees or salamanders.  These particular compounds have a history and effects that are not difficult for us to research, and we should become aware of their impacts upon the planet quickly enough.  Many of us already are.  The fact is that organophosphates have their origins as nerve gas agents in the pre-World War II era, and in theory their use has been reduced but hardly eliminated.  Residential use is apparently no longer permissible in the United States, but commercial usage still is.  This raises questions on what real effect any such “restrictive” legislation has had.

The neonicotinoids are promoted as a generally safer alternative to the organophosphates, but they are hardly without controversy as well.  They too have strong associations with CCD in the research that is ongoing.  They also are neuro-active insecticides.

It would seem to me that we all have a job to do in getting up to speed on the source, distribution and levels of exposures to insecticide and insecticide related compounds.  A greater awareness of toxins in our environment, in general, also seems in order.  If our general environment has been affected to a degree that has avoided confrontation  thus far, then we need to face the music as quickly as possible.  I trust that we understand the benefits of both rationality and aggressiveness when serious issues face us, and this may be another such time.  I hope that I will be able to dismiss this report in due time; at this time, I cannot.


Clifford E Carnicom
Nov 05, 2015

Born Clifford Bruce Stewart
Jan 19, 1953


Additional Notes:

The preliminary functional group assignments being made to the absorption peaks at this time are as follows (cm-1):

~ 3322 : Amine, Alkynes (R2NH considered)
~ 2921 : CH2 (methylene)
~ 2854 : CH2 (methylene)
~1739 : Ester (RCOOR, 6 ring considered)
~1447 : Sulfate (S=O considered)
~1149 : Phosphate (Phosphate ester, organophosphate considered)
~1072 : Phosphine, amine, ester, thiocarbonyl
~677  : Alkenes, aklynes, amine, alkyl halide

The assignments will be revised or refined as circumstances and sample collections permit, however, as a group they appear to provide a distinctive organic signature.  A structural model may be developed at a future date.

Some chemical compounds which may share some similar properties to that under consideration here include, for example, (not all elements included in any listed compound; only for reference comparison purposes):

p-chlorophenyl (3-phenoxypropyl)carbamate
N-(1-naphthylsulfonyl)-L-phenylalanyl chloride
2,2,2-trichloroethyl 2-(2-benzothiazolyl)dithio-alpha-isopropenyl-4-oxo-3-phenylacetamido-1-azetidineacetate
cytidine monophosphate

per :
SDBSWeb : (National Institute of Advanced Industrial Science and Technology, Nov 06 2015)

Secondary Rainwater Analysis : Organics & Inorganics

Secondary Rainwater Analysis :
Organics & Inorganics

Clifford E Carnicom
Nov 04 2015


A second rainwater sample has been evaluated. On this occasion, both organic and inorganic attributes of the sample have been examined.  Although the sample investigated is of much larger volume, the results demonstrate an essentially equivalent level of aluminum present to that defined within the earlier report, i.e., approximately 2 PPM.  This magnitude exceeds the US Environmental Protection Agency recommended standards for aluminum in drinking factor by roughly a factor of 10. 

In addition, various organic attributes of the sample are introduced within this report.


 Concentrated Rain Sample under Study in this Report
Distilled Water Reference on Left, Concentrated Rainfall to Right

Residual Solid Materials from the Rainwater Sample of this Study

The volume of the sample collected is approximately 6.5 liters over a three day heavy storm period, collected in clean containers that are were exposed to open sky.  The sample was concentrated by evaporation under modest heat to approximately 6% of the original volume.  It is apparent from visual inspection and by visible light spectrometry that the concentrated rainfall sample is not transparent and that it does contain materials to some degree.

Visible Light Spectrum Rainfall2

Visible light spectrum of the concentrated rainfall sample.  The increase in absorption in the lower ranges of visible light correspond to the yellow and yellow-green colors that are observed with the sample.
The pH of the concentrated sample is recorded at 8.5; this value is surprisingly alkaline and indicates the presence of substantial hydroxide ions in solution.  The pH of the solution prior to concentration measures at 7.5; this also must be registered as highly alkaline under the circumstances.

The pH of  ‘natural’ rain water has been discussed in earlier papers and its relationship to the expected value of 5.7 due to the presence of carbonic acid in the atmosphere (carbon dioxide and water).  The departure of natural rainwater from the theoretical neutrality of 7.0 is one aspect of the pH studies that I conducted in conjunction with numerous citizens across the nation some years ago, and these reports remain available.  The current finding is remarkably alkaline and, by itself, is indicative of fundamental acid-base change in the chemistry of the atmosphere.

From those early reports, it may be wise to recall the words of Paul Crutzen, Nobel Prize winner for Chemistry (Atmosphere, Climate and Change, 1995), who stated that the most important chemical attribute of precipitation is indeed the pH value.  It behooves us, as a species, to act rather quickly on any reasonable claim to a significant change in fundamental atmospheric chemistry that may exist.  It must be acknowledged that these same claims now prevail over decades of time, and that any dismissal as an aberration of no consequence is unjustifiably diminutive.

The sample has been examined again for the existence of trace metals using the method of differential cyclic chronopotentiometry, as described in the earlier report. The results are essentially identical to that of the earlier report, and once again the signature of a soluble form of aluminum is detected . The sample in this case, however, is of much larger volume, was collected over a longer duration, and was more highly concentrated that that in the preliminary report.

The concentration level was again determined, and the analysis indicates a level of soluble aluminum within the rainwater sample at 2.0 PPM.  This compares quite closely with the earlier sample result of approximately 2.4 PPM . This determination once again takes into account the concentration process that has been applied to the sample for testing sensitivity purposes.

Two facts bear repeating here:

First, this value exceeds the US Environmental Protection Agency (EPA) standards for drinking water by roughly a factor of 10, again using the most conservative approach possible that can be taken.

Second, the previously referenced U.S. Geological Survey statement from the year of 1967 is valuable both in relation to evaluating the EPA standards as well as assessing the expectations of aluminum concentrations in natural waters:


There is now a necessity to include an additional aspect of the rainfall analysis that has made its presence known more clearly.  This is the case of biologicals.  It is a fact, that in addition to the repeated detection of a trace metal at questionable levels, certain organic constituents are coming to the fore.   The test results are repeatable at this point and these organics will eventually require an equal accounting for their existence.  I will not enter into an extended discussion of their potential significance at this time, as the first and necessary step is to place on the table that which must be confronted.  My introductory suggestion at this point is to become aware of a previous paper on this site, entitled “A New Biology” to gain some familiarity with the scope of the issue . It is fair to say that along with changes of chemistry in this planet, we must also confront certain changes in biology that are in place.  The history of this planet, the cosmos, life and our own species is dynamic, and intelligence itself is partially expressed in the ability to adapt to changing circumstances.  We are in the process, whether we like it or not, of learning if and how quickly we can adapt to changes that have and are taking place, induced or otherwise.  We may also choose whether to participate in the process (hopefully for the betterment of the world, as opposed to its detriment), or if we shall remain ignorant in an effort to ensconce ourselves in a purported comfort zone.

The methods of examination to be presented here are twofold: that of microscopy and that of infrared spectroscopy.  Here are some some images that relate to the fact of the matter; they are repeated in both samples that have been examined:


Low Power (~200x) of Biological Filaments Contained in
Residual Materials from Concentrated Rainwater Samples
(The colors of the filaments are a unique characteristic (commonly red and blue) and they exist as an aid to identification with low power microscopy)


High Power (~5000x) of Biological Filaments Contained in
Residual Materials from Concentrated Rainwater Samples

These images will not be elaborated on in detail at this time, as it may require a period of time to examine the information that has come forth here.  They most certainly indicate a biological nature that shares a common origin with many of the research topics that have evolved on this site over the years.  It may be worthwhile to begin by becoming familiar with the ‘environmental filament’ issue that is so thoroughly examined on this site.  Since it seems clear that we are indeed dealing with an ‘environmental contaminant’ of sorts, the history of communication with the U.S. Environmental Protection Agency may also be worthy of review.

It would also seem to be the case that a significant portion of the residual material is inorganic as well, as in an insoluble metallic form.  It may be that the insoluble residual material may be composed in part as an organometallic complex, based upon historical findings.

Regardless of the source or impact of these materials, it does seem to fair to state that an accounting for their existence in the atmosphere and rainfall is deserved.  Each of us may wish to play a part in seeking the answers to such issues and questions before us all.  I wish for this to happen, as I suspect many of us know that it is the right thing to do.


Clifford E Carnicom
November 01, 2015.

Born Clifford Bruce Stewart
January 19, 1953.

Preliminary Rainwater Analysis : Aluminum Concentration

Preliminary Rainwater Analysis :
Aluminum Concentration

Clifford E Carnicom
Nov 02 2015


A method and means to identify the species and concentration of several different trace metals in ionic form has been established.  The method employed is that of differential cyclic chronopotentiometry, which is a subset of the science of voltammetry.  The brief paper presents a preliminary examination of a rainwater sample for the existence of trace metals.  The sample under examination shows the existence of aluminum in a soluble form.  An estimate of the concentration level of the aluminum has been made; this level exceeds that of the recommended standards for drinking water.  The results indicate that public concerns about the toxicity levels of certain trace metals in the general environment are warranted, and that a more thorough evaluation of the state of atmospheric quality by the responsible agencies is required.

Rainwater Sample of this Study Collected under “Clean” Conditions
Note that Visible Pollution is also Evident

The determination of  trace metals can be an expensive and sophisticated proposition.  One of the more modern methods of detection at trace levels involves the use of Inductively Coupled Plasma (ICP); such means and skill sets are not practiced by the public under normal circumstances.  The determination of inorganic compounds at trace levels has always presented a serious challenge to this Institute, and in the past all such efforts have been relegated to that which can be gleaned primarily from qualitative testing methods.  One interesting alternative, with a long history and of increasing importance, is the science of voltammetry.  Many are familiar with the fact that elements and compounds have unique electromagnetic spectrums, such as those employed in the disciplines of spectroscopy including, for example, infrared spectrometry and atomic absorption.  It is valuable to know that many of these same elements also have an ‘electrochemical signature’, and that they behave in unique and identifiable ways when exposed to variations in voltage and current.  It is from this fact that voltammetry was born, and its origin dates back to the the days of Michael Faraday.  The basic principle of voltammetry is to examine the relationships of oxidation and reduction within a medium or a reaction; there are numerous variations upon the specifics of this theme.  Voltammetry equipment is dramatically more modest in cost than ICP and mass spectrometry, and yet it can still produce usable results that are, on many occasions, commensurate with the more advanced equipment and technology.  Such equipment, in is most basic form, is now employed at the Institute and it is yielding promising results in the important domain of inorganic analysis, such as metals and halogens.

The study here refers only to an inorganic analysis that has been made; at a later date a presentation on biological aspects of the rainwater sample will occur as time and circumstances permit.

The rain sample was collected on Oct 30 2015 with new and clean containers with a clear path to the sky above.  The sample was then evaporated to 33% of the original volume for the purpose of increasing the concentration level sufficient for testing purposes.  The sample was compared to a control volume of distilled water.

The potentiostat used in the voltammetry work is a CV-27 model from Bioanalytical Sciences. The unit has passed all test procedures as described in the manual. The output from the potentiostat is coupled to a Pico 2000 series digital oscilloscope, whereby both voltage input and output can be displayed as a function of time. The basic mode of operation for the testing process is therefore one of chronopotentiometry.

A series of calibration tests were made with a variety of trace metals, including calcium, magnesium, sodium, potassium, iron and aluminum.

The goals of the investigations include both the ability to identify the species as well as concentration; both goals have been achieved with the above elements in an ionic state in sufficient concentration, i.e., on the order of a few parts per million (PPM).  The work will extend to other species and combinations thereof in the future.

The particular variation of chronopotentiometry that has been utilized is that of cyclic chronopotentiometry, i.e, the alternating sweep between positive and negative voltages in the effort to identify the peak potential that characterizes the redox reaction of the particular element.

In addition, it has been found that the derivative of the chronopotentiogram is a key and critical factor in the determination of the species.  A careful analysis of the derivative of the cyclic chronopotentiogram can be used with favor to identify the peak potential of the element.

When this point is identified and collated with the identifying element, concentration levels can also be established if a set of known standards is available. Concentration determinations on the order of a few parts per million have been achieved on multiple occasions.

Further careful evaluation of the derivative of the cyclic chronopotentiogram in combination with variable voltage sweeps can be used to identify separate components within a mixture of ionic species; this has been accomplished with a combination of three elements in ionic form in aqueous media to date.

The current work, under these preliminary conditions and examinations, leads to an assessment of a concentration level estimate of aluminum (+3, ionic state) within the rain sample at approximately 2.5 PPM.  A conservative approach in all manners of examination has been adopted in the preparation of this estimate, and the condensing of the sample is accounted for.

The Environmental Protection Agency in 2012 lists the secondary regulations for aluminum in drinking water as being within the range of 0.05 to 0.2 mg/L.  This corresponds to a range of 0.05 to 0.2 PPM for this same standard.  It is an interesting observation within the same report that Secondary Drinking Water Regulations exist as non-enforceable federal guidelines. The wisdom of that classification process can be determined by the reader.

Continuing with the most conservative approach possible, one is led to the assessment that this particular rain sample from a rural location in northern Idaho exceeds the EPA drinking water standard and health advisory by roughly a factor of 12.

The following reference statement from the United States Geological Survey (Bulletin 1827-A, 1967) may be of interest in the evaluation of importance that is to take place:


It is a point of interest that many individuals have ascribed the detection of aluminum within the atmosphere over a period of many years to my name.  Such was never the case.  My earlier work did indeed establish the precept that ionizable metallic salts are at the core of atmospheric pollution that we now live under, but the testing of aluminum, specifically, was not a part of that process.  The chemistry of aluminum is quite different from that of the alkali earth metals, and the documentation of its existence by others has always raised intriguing questions of physics. Prior to this current work, most of the inorganic analyses that I have made have been restricted to qualitative tests.  No means of testing aluminum at the trace levels has existed for the Institute prior to this occasion.  Hopefully, this situation is now mildly improved with the current voltammetric studies.  This paper adds itself to a long list of documented actions by the citizenry on the consideration that aluminum is certainly, and has been, entitled to.

As a starting point, we might wish to consider the role that aluminum may play within a geoengineered environment, and it may be worthwhile to look at the exothermic energetics of nano-particulates of aluminum under exposure to moisture.  It raises some tantalizing prospects for additional capabilities of an induced or artificial plasma state.

It is also an observation that visible pollutants in rainwater may be most pronounced with the advent of a storm. This is logical, and this has certainly been observed in the cases of excessive fires in this region.  Time will tell if it is the circumstance of other samples.  It remains to be seen how the gradation of pollutants varies with respect to the duration of the rainfall.  Nevertheless, this study does exist as a valid data point and the merit of consideration is not weakened by any progression of dilution.  The concentration gradient with respect to storm length for invisible pollutants, such as those in ionic form, remains as a topic of equal interest for the future.

There is, of course, considerable debate on the issue of the sources of contamination within our water supplies on this planet.  I will not engage in that debate in this paper, as the purpose here is to simply provide another data point of reference that may be of service in helping to establish the accountability that is required.  There are arguments by some that wish to frame a state of ‘normalcy’ for us, regardless of the level of contamination that as a species we now infest ourselves with.  Regardless of various machinations that may be in vogue, we may all ask the questions of where standards evolve from, and whether or not we knowingly wish to deny the legacy of health knowledge that has been acquired over decades, if not centuries.  We should also be called upon to use our united common sense and intuition, pray coupled with the best scientific information available, to act as stewards for our future, and to be worthy of such a title.

Clifford E Carnicom
November 01, 2015.

Born Clifford Bruce Stewart
January 19, 1953.


Morgellons : A Working Hypothesis
Neural, Thyroid, Liver, Oxygen, Protein and Iron Disruption
(Link to Parts I, II, III – Click Here)


Clifford E Carnicom
Dec 18 2013

Art work courtesy of David Dees with permission.

Note: I am not offering any medical advice or diagnosis with the presentation of this information. I am acting solely as an independent researcher providing the results of extended observation and analysis of unusual biological conditions that are evident.  Each individual must work with their own health professional to establish any appropriate course of action and any health related comments in this paper are solely for informational purposes and they are from my own perspective.


This paper seeks to identify a host of organic compounds that are likely to comprise the core physical structure of biologically produced filaments characteristic of the Morgellons condition.  A biological oral filament sample will be analyzed for the presence of candidate organic functional groups using the methods of infrared spectrophotometry.  Potential health impacts from these same core structures are examined and compared to the observed , reported and documented symptoms (in part) of this same condition.  Potential mitigating strategies, from a research perspective only, are discussed.

A body of evidence, accumulated over a period of several years, reveals that the Morgellons condition is likely characterized by a host of serious physiological and metabolic imbalances.  These imbalances are caused by the  disruption of a variety of major body processes including, as a minimum, the regulation of metabolism by the thyroid, potential liver enlargement, a decrease of oxygen in the circulatory system, the utilization of amino acids important to the body, the oxidation of iron and a potential impact to neural pathways.  The impact of this degradation to human health can be concluded to be serious, debilitating and potentially lethal in the cumulative sense; the reports of those who suffer from the condition are in alignment with these conclusions.  This paper will summarize the body of work and chronology which leads to this more comprehensive hypothesis.

The health, medical and governmental communities will again be invited to offer their expertise and contributions , as well as to assume their role of responsibility and the obligations of their professions to serve the public.

This paper will be divided into three phases:

I. Identification of the functional groups / components

II. Potential health impacts of the various functional groups identified.

III. Potential mitigating strategies (research-based)



We now begin the final phase of this paper, and this is to introduce, recall and compile a host of strategies and considerations that may be helpful to mitigate some of the impacts upon health by the Morgellons condition.  Some of the work that has been done previously will also be incorporated into and repeated within this section; much of this work remains especially valuable and relevant here as well.  It is important to understand that this information is derived from an individual research standpoint only, and that it does not represent any medical advice or diagnosis whatsoever.  The usual disclaimer and caveat will be repeated before we begin the conversation:

Note: I am not offering any medical advice or diagnosis with the presentation of this information. I am acting solely as an independent researcher providing the results of extended observation and analysis of unusual biological conditions that are evident.  Each individual must work with their own health professional to establish any appropriate course of action and any health related comments in this paper are solely for informational purposes and they are from my own perspective.

Before we begin in earnest, it is worthwhile to examine the basic mechanisms of disease.  In my own journey of study and discovery in the field of health and disease, it astounds me that these principles are actually so well established and yet they are often not understood and applied.  There may be a fairly broad gap between what has been understood for some time and what the public is generally aware of with respect to disease; it is hopeful that this situation continues to improve.  What especially interests me is that these principles exist irrespective of the particular condition or disease examined; we often think of each situation as being so unique and complex that we think that we can only make headway with advanced and specialized knowledge.  This is not necessarily the case if we take the list that follows to heart.  We find these “mechanisms” listed in the standard textbooks of pathology and, in particular, within the very first chapter of the well established tome entitled, Robbins Pathological Basis of Disease57, 4th Edition.  It is succinctly stated that:

“Although it is not always possible to determine the precise biochemical site of action of an injurious agent, four intracellular systems are particularly vulnerable:

(a) maintenance of the integrity of cell membranes

(b) aerobic respiration

(c) synthesis of enzymic and structural proteins and

(d) preservation of the integrity of the genetic apparatus of the cell.”

What we have been given here close to 25 years ago, if we care to address it, is the basis of disease in the body.  The statement is not qualified with respect to what type of disease is taking place, it is the basis of disease itself.  From my studies, I find no important exceptions to this as it applies to the so-called “Morgellons” condition.  

We can all interpret this in our own light, but my rudimentary interpretation is that to remain healthy:

1. We must remain intact and structurally sound at a cellular level.

2. We must use oxygen efficiently and effectively in our bodies, as respiration is the source of all energy to the body.

3.  We must continue to repair the actual structures of the body to compensate for decay and age.

4. We must be able to reproduce in a healthy fashion to flourish and prosper as a species.  

This is the challenge that we must assume to combat disease or ill health, regardless of what the particular situation or circumstances are.  It is no different here, at the most basic level of understanding, from the case of harm in general.  Of course we seek to be specific as to how this is done under the specific plight of the Morgellons condition, but it is rather astounding how evident that course is when armed with the most rudimentary knowledge of pathology.  Dr. Stanley Robbins will also get us off to a good start on this topic58, with his equally succinct listing of causative agents, such as physical agents, chemical agents and drugs, infectious agents, immune responses, genetic damage and nutritional imbalances.  We should never miss this grand view before becoming engrossed in the detail.  

I have spoken earlier to those that seek a simple pill in life to take care of the complexities that are before us; I am not your person to listen to for a myriad of reasons.  My course of research is one that seeks the fundamental understanding of the situation and that seeks to make this information accessible to all.  Remedies to problems as needed must, therefore, also be accessible to all – at least to the highest degree possible.  Specialized drugs and technologies are under the purview of others with resources, means and motive.  You must seek them elsewhere.  The work of this Institute is to research and educate on behalf of the general welfare and public with the resources that the public makes available to us.

Keeping the above foundation in mind at all times, let us go to work on the specifics.  It is helpful to have the master list that has evolved before us again.  This list basically identifies potential causative agents or mechanisms in conjunction with potential heath impacts (either reported or research-based).  This master list, as formulated, will have numerous overlaps and redundancies occurring between the two sets, and it is not to be viewed in a style of one-to-one correspondence.  Let us see if we can make some headway after the table is reviewed again:

Candidate Functional Groups or Constituent Identified within the Biological Filaments:
(potential correlations are  established at this stage)

Reported, Observed or Research-Based Candidate Health Impacts or Symptoms of the Morgellons Condition:
(potential correlations are  established at this stage)

(Fe+3 in the more highly oxidized state)

Bacterial or Bacterial-Like (Chlamydia P. or Chlamydia P.-like) Repeating Structure within both Blood and Filaments

Amino Acid Deficiency – in general

Specific Amino Acid: Cysteine

Specific Amino Acid : Histidine


Carboxylic Acids


Aromatic substituted Alkenes

Aromatic substituted Amines




Alkyl Halides


Oxygen deprivation;diminished oxygen carrying capacity of the blood
[Iron & Bacterial or Bacterial-Like Structure,
Amino Acid Deficiency, Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines]

Significant oral filament production; the presence of filament structures (ferric iron – anthocyanin complexes) within oral samples.  (red wine test)
[Iron & Bacterial or Bacterial-Like Structure,
Phenols – Aromatic Amines]


Skin-borne filament production; skin manifestation at the more developed levels (the skin is an excretory organ).
[Iron & Bacterial or Bacterial-Like Structure]


Extended or Chronic Fatigue
[Iron & Bacterial or Bacterial-Like Structure,
Amino Acid Deficiency, Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines]

Hair alterations, i.e., texture, thickness, loss of hair
[Iron & Bacterial or Bacterial-Like Structure,
Amino Acid Deficiency, Cysteine Deficiency]


Gastro-intestinal imbalance
[Iron & Bacterial or Bacterial-Like Structure,
Amino Acid Deficiency, Histidine Deficiency, Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines, Alkyl Halides – Halogens]

Immune system breakdown
[Iron & Bacterial or Bacterial-Like Structure, Amino Acid Deficiency, Histidine Deficiency, Cysteine Deficiency, Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines, Alkyl Halides – Halogens] 

The impact of increased oxidation, greater free radical presence and their damaging effects upon the body.
[Iron & Bacterial or Bacterial-Like Structure,
Amino Acid Deficiency, Cysteine Deficiency,  Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines, Alkyl Halides – Halogens]


Lower energy levels due to interference in the ATP production cycle; greater fatigue
(iron is a transport medium for electrons within the cells)
[Iron & Bacterial or Bacterial-Like Structure,
Amino Acid Deficiency]


Any bacterial forms that infect the blood requires iron if it is to grow and reproduce.
[Iron & Bacterial or Bacterial-Like Structure]


The smoking population may exhibit an increased incidence of the condition due to additional oxygen inhibition within the blood.
[Iron & Bacterial or Bacterial-Like Structure]


Specific blood abnormalities
[Iron & Bacterial or Bacterial-Like Structure,
Histidine Deficiency,Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Phenols – Aromatic Amines]


Metabolic disruption
[Iron & Bacterial or Bacterial-Like Structure, Amino Acid Deficiency, Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Phenols – Aromatic Amines, Alkyl Halides – Halogens]


Liver toxicity, gall bladder and bile duct complications.
(binding of oxidized iron to toxic molecules, e.g., cyanide and carbon monoxide)
[Iron & Bacterial or Bacterial-Like Structure,
Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Alkyl Halides – Halogens]


An increased level of acidity in the body.
[Iron & Bacterial or Bacterial-Like Structure,
Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines, Phenols – Aromatic Amines]


Skin lesions
[Amino Acid Deficiency, Cysteine Deficiency, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines]


Chronic Decreased Body Temperature
[Amino Acid Deficiency, Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General]


Neurological Impairment (e.g., blurred vision, slurred speech, ringing of ears (tinnitus), loss of coordination, loss of strength)
[Amino Acid Deficiency, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines]


Cognitive impairment, i.e., mental confusion, inability to concentrate, short term memory loss, “brain fog”
[Amino Acid Deficiency, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines, Phenols – Aromatic Amines]


Joint Pain
[Amino Acid Deficiency, Histidine Deficiency, Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Carboxylic Acids – Over Acidity – Acidosis]


Liver Toxicity
[Amino Acid Deficiency, Cysteine Deficiency, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines]


Respiratory problems, including proclivities toward a chronic cough or walking pneumonia-like symptoms
[Iron & Bacterial or Bacterial-Like Structure, Aromatic Amines – Halogenated Aromatic Amines – Thyroid Inhibitors in General, Phenols – Aromatic Amines, Alkyl Halides – Halogens]


The presence of a bacterial-like component (chlamydia-like) within or surrounding the red blood cells
[Iron & Bacterial or Bacterial-Like Structure, Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines]


Unusual or extreme dental issues; tooth decay or loss
[Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines]

Chronic itching of the skin
[Carboxylic Acids – Over Acidity – Acidosis, Phenols – Aromatic Amines]

Associations between oxygen deprivation, glycolysis, anaerobic respiration, cancer, energy production (ATP), and intracellular acidity
[Carboxylic Acids – Over Acidity – Acidosis]

Research indicates the urinary tract may be equally affected with the presence of the filament structures
[Alkyl Halides – Halogens]

On a macro scale, we can see that some of the more obvious issues to be addressed concern iron disruption, amino acid presence and protein rebuilding, acidity, oxidative stress, availability of oxygen, thyroid and metabolism issues, halogen toxicity and substitution concerns, joint and skeletal integrity and elasticity, blood and cellular integrity, and potential neural disruption.  Unfortunately, the list is not exhaustive but it is representative of some of the health concerns that have been brought to the forefront and reported on.  

One of the interesting prospects of mitigation is that improving a limited set of disrupting influences may have benefits that extend to the wider system of health.  It might seem overwhelming to address such an array of problems, but the more that is understood between the relationships of mitigation, the greater are the chances of improvement to health on the whole.  We must all start somewhere when we begin to assume greater responsibility for our awareness and state of health; this beginning can basically become a way of life rather than a fix to a singular problem.

Let’s begin with the iron problem, as it has been discussed extensively59,60,61 and it remains as a paramount issue.  If it is accepted that iron interference is taking place, what course(s) of action might exist?  Studying these previous papers, it can be seen that a fair degree of effort has already been extended to this question.  It is appropriate to recall some of this information as follows:

1. ” Increasing the utilization and absorption of existing iron within the body.  Iron is certainly one of the most important elements of the body.  Referring to the Linus Pauling Institute,

“Iron has the longest and best described history among all the micronutrients. It is a key element in the metabolism of almost all living organisms. In humans, iron is an essential component of hundreds of proteins and enzymes.”

One of the findings from the study of coordination chemistry described above is that iron has the ability to bond with numerous other molecules.  For example, iron (in the Fe2+ state) preferentially bonds to oxygen.  If the iron is altered to the Fe(3+) state. it will no longer bond to oxygen.  In this modified state, the iron will then form additional bonds to other molecules, many of which are harmful as has also been described above.  The idea of a chelator is to keep the oxygen bound in a protected state where it can not bind so easily with other, often harmful, molecules.  Heme itself, within hemoglobin, is a classic example of a chelator.  If our iron has been altered to where it becomes free or bound to other molecules (potentially harmful ligands), the solution to that problem would not seem to be to take more iron, any more than increasing the oxygen intake is expected to resolve a problem of oxidation.

The more effective solution would appear to be to keep the iron in a chelated state, where it is bound and protected by the expected molecules and proteins such as heme in the body.  This therefore suggests that increased attention would be devoted to the study and role of chelators in human health.  It does not seem reasonable that we would automatically pursue a path of increasing iron intake; indeed this process can be quite harmful and dangerous to human health.  Again, the importance of consultation with the medical professionals of choice is unequivocally stated; the stakes of the issues we are speaking of are of the highest importance.

2. The inhibition of the growth of iron-consuming bacteria (and bacteria-archea like) forms.

We know now that the organism uses iron for its existence and growth.  It appears that iron in the further oxidized state (i.e, Fe3+) is of primary benefit to the organism.  We also know, in retrospect, that iron is a critical metabolic element within many of the bacteria (or bacteria-archaea like forms).  One strategy that develops with such organism is that of inhibiting the ability of the organism to access or metabolize the iron.  This once again brings up the idea of a chelator.  This topic has also been discussed in an earlier paper, and introduced the role of human breast milk and its resistance to bacterial forms in infant growth96. Lactoferrin (found in whey) was identified as a potential strong chelating protein within that research.  Transferrin is another protein chelator within the human digestive tract that serves a similar purpose, i.e., binding of the iron and consequently it becomes less accessible to iron-consuming bacteria (or bacteria-archea like forms).”

We also recall from the earlier papers mentioned an important discussion about the potential benefits of Vitamin C, NAC (N-Acetyl Cysteine) and glutathione.  These three compounds are powerful anti-oxidants and they also relate directly to the issue of oxidative stress in addition to that of iron disruption:

“Three methods that appear to interfere with the molecular bonding of the iron-dipeptide complex that is now understood to be characteristic of the “Morgellons” growth structure have been established and identified.  The iron-protein complex is believed to be of, or similar to, the “Rieske Protein” (iron-sulfur) form.  These three methods also appear to be variably successful in reducing the oxidation state of the encapsulated iron from the Fe(III) state to the Fe(II) state.  The discovered methods involve the use of ascorbic acid (Vitamin C), N-acetyl cysteine (NAC) and glutathione.  The results of applying glutathione appear to be especially promising at this time, as it appears that a major disruption in the bond structure has taken place after approximately 72 hours.  The methods have been established and verified through visual, chemical and spectroscopic methods and each has an effect independent of the others.  The hypothesis to be made here is that the growth of the organism itself may be interfered with as a result of this work.

The reader is advised to consult the Institute referenced papers for the detailed information that underlies the excerpts given:

Morgellons : In the Laboratory

Morgellons : A Thesis

Morgellons, The Breaking of Bonds and the Reduction of Iron

A Carnicom Institute  research discussion on this and related issues has also been made available to the public previously.  In addition, a series of videos that discuss the importance of glutathione (and its precursors) has also been included within the earlier papers.

Listen to a Research Discussion on This Topic

View A Series of Informational YouTube Videos on Glutathione
(Note the references to N-Acetyl Cysteine (NAC) and whey(lactoferrin) in the second video of the series(Dr. Mark Hyman))
(No endorsements of products to be implied or stated herein)

The question of whether to take a supplement of iron or not will not be discussed here; this harkens to the pill philosophy discussed earlier.  This question will not only apply to iron supplements, it will apply to any and all questions that will be addressed concerning supplements of any kind.  I will report on the research facts available to us all; we must then assume our individual responsibilities of action or discussion with the health professionals and advisors of our choice.  It is not my role or position to be involved in any individual concerns or requests.  I am not acting in any medical capacity whatsoever; I am acting fully and completely as an independent researcher.  

The importance of the honest and dedicated involvement of the health and medical communities should be obvious to all of us; I encourage you to force this issue as it deserves.

In the particular case of iron supplements, there are risk involved as with most to all things that human beings can ingest.  Specifically, unwarranted iron consumption can lead to:

“Iron supplements can cause indigestion, stomach pain, constipation, diarrhea, nausea, vomiting, back pain, muscle pain, chest pain, chills, lightheadedness and fainting, rapid heartbeat, fever, sweating, flushing, headache, metal taste, numbness or tingling in the hands and feet, rash and breathing problems62.”

In the case of high dosages, it can:

“High doses of iron can cause stomach and intestinal problems, liver failure, dangerously low blood pressure and death. Iron poisoning is the most common cause of poisoning deaths in children, according to Medline Plus. Symptoms of iron poisoning include bloody diarrhea, fever, nausea, sharp stomach pain and severe vomiting — possibly of blood — a blue tint to the lips, nails and palms, seizures, pale or clammy skin, shallow or rapid breathing, extreme fatigue and a weakened or fast heartbeat63.”

Obviously, it would seem to be of greater interest to efficiently utilize existing iron within the body rather than to assume the addition of iron automatically addresses the problem.  It has also been discussed in previous papers that Vitamin C (ascorbic acid), in addition to being a powerful antioxidant, helps to increase the absorption of iron into the body.  From a current reference, we can see that there are two methods by which this occurs64:

1.  Vitamin C (ascorbic acid) helps to prevent the formation of non-soluble iron forms.

2.  Vitamin C reduces iron from the ferric (Fe3+) to the ferrous (Fe2+) state.

The importance of this latter statement must be emphasized again, and it is the very basis of the paper entitled “The Breaking of Bonds and the Reduction of Iron” presented in November of 201265.

We can see, therefore, that iron in the ferrous (Fe2+) state is generally going to be more bio-available in the ferric state vs. in the ferric state, both from the standpoint of iron-oxygen binding in the blood as well as in the direct absorption of iron by mucosal cells.  It has been shown in the laboratory through Institute research that vitamin C, NAC (N-acetyl cysteine) and glutathione have each been effective in this reduction process from the ferric to the ferrous state.  It would be worthwhile to review the details of the Institute reference papers that have been cited in this report; the discussions related to glutathione and its precursors (as opposed to direct supplementation) are especially important (i.e., the use of NAC).
The roles of chelation as well as anti-oxidants, as they have been discussed, should also be given full consideration for their potential benefits prior to assuming supplementation is a logical strategy.


Understanding the co-existence between iron and bacteria should also help in the process of setting priorities for healing.  Also, from the earlier paper66:

“A bacterium that infects the blood requires a source of iron if it is to grow and reproduce.”

“Like their human hosts, bacteria need iron to survive and they must obtain that iron from the environment.  While humans obtain iron primarily through the food they eat, bacteria have evolved complex and diverse mechanisms to allow them access to iron…  Iron is the single most important micronutrient bacteria need to survive… understanding how these bacteria survived within us is a critical element of learning how to defeat them”We may, therefore conclude that:

The elimination of bacterial infections in the body would, therefore, obviously be beneficial in increasing the utilization of existing iron; additional iron via a supplement might simply act as a facilitating nutrient to detrimental bacterial forms.

It is also of much interest to present within in this research that NAC (N-acetyl cysteine) has two additional benefits in addition to its effectiveness as an anti-oxidant.  In the following paper by the pathologist David Wheldon it is clearly stated that NAC also68:

1. has the ability to destroy chlamydial elementary bodies.

2.  replenishes intracellular glutathione.

Those familiar with the research of this site will be aware of the extensive investigation and study that has been placed upon the “chlamydia-like” or “bacterial-like” form that has been repeatedly identified within the filament structures.   The difficulties of eliminating that particular bacterial form have also been made apparent; hence the chronic respiratory symptoms that accompany its presence.  The imperviousness of these “elementary bodies” (i.e, a spore-like form that remain dormant for extended periods) is  at the heart of that difficulty.  The use of NAC as an important precursor to the formation of glutathione (one of the most powerful anti-oxidants that exists) has also been previously discussed on this site.  The many benefits of NAC (and also its reported anecdotal success with its use with Morgellons) can now be better understood with respect to its chemistry, its specific actions of reduction (anti-oxidation) and its precursive role in the formation of glutathione.  It is also of clear and immediate interest that this same paper states that the mechanism of destruction of these elementary bodies is by the breaking of disulphide bonds within the chlamydia organism (see discussion immediately below).


We now migrate to the amino acid – protein issue, and it becomes increasingly apparent that any separation of our topics is largely artificial.  In addition to the withdrawal and diversion of iron from the body to support a parasitic life form,  the redirection of amino acids and proteins to support such a life form is an equally serious matter.  Proteins make up more than fifty-percent of our bodily constitution and they are made from amino acids; if these are interfered with in any fashion it is inevitably to our detriment.  The research evidence does indicate that such interference is taking place.  There are a minimum of three amino acids that exist at the top of the interest list, and it should not be surprising if there are others.  The three of immediate interest include cysteine, histidine and tryrosine; again, there may well be others.

The original interest in cysteine emerged from the original observations of strength of the bonds of the filament materials, both environmental and biological.  The materials, from the beginning, have shown tremendous resistance to chemical and physical agents, such as acids, alkalies and temperature.  This indicates, from the onset,  the likely existence of disulphide bonds,  which are characteristic of both cysteine and cystine forms.  Cysteine is an amino acid that is characterized by the presence of sulfur, which can then further form disulphide bonds.   For example, hair is largely composed of keratin (a protein), and this protein is largely composed of such disulphide bonds.  This is one reason that hair is similarly so resistant to chemical breakdown.  The presence of cysteine with the filament forms (environmental and biological) has been further supported by direct observation via visible light spectrophotometry in combination with ninhydrin testing.  The presence of amines (building blocks of amino acids) has been further confirmed with infra-red spectrophotometry described in this report.  

The interest in histidine has also come about with the use of visible light spectrophotometry in combination with ninhydrin; please refer to the earlier paper entitled “Amino Acids Verified” for additional details of this earlier project67.  This interest has also been extended with the knowledge of the existence of the histidine side chain in the heme (hemoglobin) molecule coupled with the observation of the extensive breakdown in the integrity of the red blood cells (erythrocytes).  There is ample reason to focus on the likely existence of histidine (an amino acid) as a part of the biological filament growth form.

The interest in tryosine comes solely from the current work with IR spectrometry and the subsequent relationships that have been identified with both dopamine (a neuro-transmitter) and thyroxine (a primary metabolic hormone of the thyroid).  Interest in this particular amino acid is also increased due to knowledge of some of the mechanisms of aromatic chemistry, particularly the substitution reactions involving the halogens and the hydroxyl groups.  These have been discussed at length in this report and they both suggest the very real possibility of structural disturbances to both thyroxine and dopamine within the body.  In addition, the observed symptoms of the Morgellons condition are primary data points in our study and must not be denied.  The strong presence of metabolic, neural and cognitive interference in conjunction with the Morgellons condition gives, by itself, just cause to investigate any tyrosine disruptions that may be in place.  The combination of all factors above, IR observations, aromatic chemistry and reported symptoms all lend themselves to a deep investigation of the tyrosine, thyroxine, dopamine and oxidopamine issues and relationships.

An additional interest regarding collagen, a protein, has also developed prominently over the this last year especially in relation to the issue of joint pains.  Joint pains are another of the primary symptoms that are on record in association with the Morgellons condition.  These issues were introduced in a Carnicom Institute webinar presented last year and the access to it is repeated here for your listening and review:

Listen to an Institute Research Discussion on Amino-Acids – Collagen

The research interest, as a result of all of the above, now includes amino acids and proteins in general.  If there is strong evidence to show that a host of amino acids are either diverted or disrupted to support the growth of the filament structure then there is an equally strong case to consider supporting the body with those same amino acids.  Amino acids and proteins are structural features of the body that give it both form and function; these proteins are to be rebuilt if they are lacking in the body.  There should be no hesitation in promoting the use of foodstuffs in the body and the proteins are once such main group.  There are numerous methods by which one might accomplish such an increase, such as in the use of supplements, protein powders, diet and the like.  No specific recommendations on that approach will be given here, but such means are readily available for all to consider.  We have already considered whey (a particular protein form that has value with iron chelation).  Gelatin is another form of protein that is strongly associated with collagen production. Protein rich foods and/or protein powders may be additional forms of nourishment that can be considered in light of the findings.  Again, the reader has the responsibility to develop any health related strategies with the counsel of their own health practitioner and the information here is provided from a research standpoint only.


Let us turn now to the issues of oxidation, oxidative stress and free radical damage.  Our first clue that a serious issue with oxidation exists is with the repeated and definitive detection of highly oxidized iron within the biological filaments and the cultures that have been developed from them.   Iron in the blood is required to be in the Fe+2 (ferrous) state to bind to oxygen; if the iron is changed to the Fe+3 state (ferric) it will no longer bind to oxygen and the primary function of the blood  to transport oxygen transport throughout the body is no longer properly fulfilled.  The iron in the biological filament is in the Fe+3 state; this means that an electron has been stolen from the iron in the blood in the Fe+2 state, and this represents a transfer in energy, in essence, from the blood of the human to support the growth of the organism.

Another more direct method to investigate the state of oxygen carrying capacity in the body is to look at the blood under sufficient magnification.  It has long been reported on this site that the integrity of the blood cells and the presence of the chlamydia-like bacterial structures within the blood are direct windows into the health impacts from the Morgellons condition.  Please refer to the earlier paper (amongst others) entitled “A Mechanism of Blood Damage”, authored in December of 200969. In the table below are two blood slides of the same individual over a period of several years.  The image to the left is during the earlier investigations of the blood as they relate to the Morgellons condition and as they were extensively reported upon within this site.  The image to the right is of this same individual in a more contemporary state after considerations of the research within this site have been applied.  Knowledge of the benefits of anti-oxidation strategies, along with the strategies to eliminate free radicals within the body, can potentially be demonstrated with these images as examples.

Examples of variability in general red blood cell integrity and the penetration of the cell membrane by the chlamydia-like organism within the blood.  The oxygen carrying capacity of the blood is severely impacted by this breakdown in cellular integrity.  The role of anti-oxidants and free-radical scavengers may be worthy of consideration in the improvements that are demonstrated in the image to the right.  These images are of the same individual over a period of several years of research.  It is of interest that the chlamydia-like structures appear to remain in the serum external to the cells in the image to the right; they do not appear, however, to be successful in breaching the cell membrane as they do in the image to the left.  It is presumed that the state of the immune system is a primary factor in the defensive effectiveness.

It is also of passing interest that a recently acquired commercially prepared human blood slide also shows this same detrimental blood condition upon sufficient magnification:

A commercially prepared human blood slide presumably representative of the general population.

Some may consider this particular human blood slide condition as a coincidence or as irrelevant; others may be aware of strong claims by this researcher over the years that the general population appears to be subject (by varying degrees) to the health impacts of the “Morgellons” condition.  Any recent statements by the National Institutes of Health (NIH) that classify “Morgellons” as a “rare condition” are in conflict with the assessment that has evolved from the research here.

Another indication of excessive oxidative stress in association with the Morgellons condition derives from a study briefly mentioned within the earlier research report, “Morgellons : A Thesis”70.  The particular section of the paper being referred to is entitled “A Proposed Spectral Project”.  In this study, albeit with a limited sample, the results strongly indicate a deficiency in oxygen carrying capacity of the blood of a set of individuals claimed to be severely impacted by the Morgellons condition.  

In addition, there is a body of anonymous functional medicine survey data made available to me that indicates severe oxidative stress conditions that are highly statistically significant within a separate set of individuals that claim to be severely affected by the Morgellons condition  

Further, the functional group analysis from this paper reveals a host of structural features (identified, implied and plausible) that form a reasonable basis for the development of significant oxidative stress.  These include (in addition to the oxidized iron – chlamydia-like presence situation), amino acid deficiencies, any cysteine deficiency,  the presence of aromatic amines (with special attention to aniline or aniline-like structures, halogenated aromatic-amines and thyroid inhibitors in general, carboxylic acids and phenols (acidosis) and alkyl halides.

If we assess that oxidative stress is likely a reality rather than a suspicion or conjecture, we then seek to address the problem with various strategies.  Let us review what these strategies might include.

The first and most obvious consideration is the liberal use of anti-oxidants to combat an oxidative stress situation.  First, we review what has already been presented once again in an earlier paper71:


 The research indicates that excessive oxidation is detrimental to health.  This topic has also been discussed previously in an earlier paper72. Common oxidizers include the bleaches, peroxides and ozone.  The research indicates, from the vantage point of this researcher, that internal use of these substances is likely to be harmful to human health.  We do not solve the problem of oxidation within the body by necessarily increasing the intake of oxygen.  Indeed, one of primary arguments of this paper is that the blood of the affected individual has been oxidized in a fashion that has the net effect of decreasing the oxygen carrying capacity of the blood.  Excessive and misplaced oxidation also creates free radicals, which as been noted, “wreak havoc in the living system.”We do not solve that problem by taking more oxygen; we work on the problem by hindering the oxidative process.  The manner in which this process is conducted in the chemical world is known as reduction.  In common terms, the appropriate term is that of an anti-oxidant, and many of us are familiar with that parlance.

 I  take stock in the following statement, again from Cotran73:

“Once free radicals are formed, how does the body get rid of them?  There are several systems that contribute to termination or inactivation of free radical reactions:

1. Antioxidants (.e.g, vitamins, glutathion, transferrin..) 

2. Enzymes.”  

The statements here are direct and understandable and come from a standard textbook in pathology. It is relatively straightforward that if a problem of excessive oxidation exists within the body, one should strongly consider the role that anti-oxidants play in reversing those effects.  It is equally inadvisable, from this researcher’s point of view, to compound the issue with the addition of known strong oxidizers internal to the body  

Vitamins, across the board (A, B, C, D, E) are powerful antioxidants.  An additional powerful antioxidant identified in the research is that of glutathion.  The role of Vitamin C (ascorbic acid) in the inhibition of the culture growth has already been described.  There remain many additional anti-oxidants of importance in human health74.



I will further discuss and present resources on the topics of oxidative stress (from a health perspective) as well as “free radicals” in more detail to further emphasize their importance.  As mentioned, oxidation is defined as the loss of electrons and reduction is defined as a gain in electrons.  The process of exchanging, transferring or sharing of electrons has already been described as being fundamental to essentially all biochemical reactions; electron transfer is at the core of biochemistry.  It  is essentially the flow of energy within living organisms.  An introduction to the importance of the oxidation stress and free radical issues as they relate to health is given as follows:


“Mounting scientific evidence may support the important role of free radicals in the development of some diseases. Free radicals are molecules or atoms that have at least one unpaired electron which usually increases the chemical reactivity of the molecule. Environmental radiation and physiological processes in the body cause free radicals to form. Free radicals can react with other molecules to cause cell damage or DNA mutation. Molecules called antioxidants protect against free radical damage. When antioxidants are ineffective, enzymes produced by the body work to repair free radical damage. Higher levels of free radicals tend to cause increased cellular damage. This effect is called oxidative stress. Oxidative stress may contribute to cardiovascular disease and cancer. Chemical compounds found in some foods may decrease the accumulated effects of oxidative stress, thus helping to prevent disease.75

As an alternative, the pathological approach of description to the relevance of oxidative stress and free radicals to health is as follows:

“One important mechanism of membrane damage…is injury introduced by free radicals, particularly by activated oxygen species.  It is emerging as a final common pathway of cell injury in such varied processes as chemical and radiation energy, oxygen and other gaseous toxicity, cellular aging, microbial killing by phagocytic cells, inflammatory damage, …and others…  Free radicals are chemical species that have a single unpaired electron in an outer orbital… the radical is extremely reactive and unstable and enters into reactions with ..proteins, lipids, carbohydrates.. and nucleic acids…Free radicals may initiated by oxidative reactions that occur during normal metabolic processes… Iron is particularly important in toxic oxygen injury… The main effects of these reactive species are on membrane, lipid bonds… of proteins and nucleotides of DNA76

Another serious consequence of oxidative stress, and one that is increasingly important within the context of this paper, is that of neural degeneration.  From the following paper on the subject of oxidative stress and neurodegenerative diseases77, we find that:

“Though, oxygen is imperative for life, imbalanced metabolism and excess reactive oxygen species (ROS) generation end into a range of disorders such as Alzheimer’s disease, Parkinson’s disease, aging and many other neural disorders….Antioxidants have a wide scope to sequester metal ions involved in neuronal plaque formation to prevent oxidative stress.  In addition, antioxidant therapy is vital in scavenging free radicals and ROS preventing neuronal degeneration in post-oxidative stress scenario.”

It is clear that the combination of any neurotoxin with that of oxidative stress, both of which are serious contenders in the research course underway, represents a serious threat to neurological health and functioning.  The list of reported, observed and research-based health impacts of the Morgellons conditions must always be at the forefront in the setting of priorities for research.  The evidence of neurological dysfunction in association with the condition deserves this spotlight in combination with the findings of this report.  It is of no small interest that the commonly (i.e., formerly so) attached “diagnosis” of “delusional parasitosis” (even by supposed medical professionals) appeared at the onset of public knowledge of the condition and that this  occurred prior to any proper investigation or research.  It is fair to ask what motives and what knowledge base were in place to support such an a priori analysis and conclusion. 

Continuing to present a series of references that further illustrates the extent of discussion with respect to oxidative stress, the following more comprehensive paper from Enrique Cadenas is also available78.  In this paper, we find further clarification on what the term oxidative stress actually means.  Metabolism, oxidation, and free radicals are an intrinsic part of the living process, and by themselves are not inherently “bad” or “good”.  Cadenas explains quite simply that an imbalance between oxidants and anti-oxidants is what defines oxidative stress.  This imbalance and “consequent damage to cell molecules constitutes the basic tenet of several pathophysiological states, including neurodegeneration, cancer, mutagenesis, cardiovascular diseases, and aging.  A summary of free-radical formation, reactions, impacts upon health and various defenses against these effects is further detailed within this report.

A parting comment from referenced sources regarding oxidative stress is in order, especially as it relates to the iron situation.  From the Alcohol, Research and Health Journal79, Wu Defeng, PhD discusses the role of metals in oxidative stress.  He states that:

“Because of iron’s critical contribution to hydroxyl radical formation, anything that increases the levels of free iron in the cells promotes ROS [Reactive Oxygen Species] and oxidative stress”

Recalling that free iron in the body is usually in the Fe+3 state (ferric) and that this form of iron is being definitively identified within the biological filament samples, it would seem as though the conditions for setting up an imbalance between oxidation and reduction (i.e., oxidative stress) have been satisfied.

It is also recommended that an earlier paper presented be reviewed at this time, entitled “Morgellons : A Discovery and a Proposal”80.  In this paper a series of direct observations and trials that show interactions between biological filament cultures, iron in different oxidation states, oxidants, antioxidants and culture growth is presented.  The results of those trials and observations are in complete accord with the expected biochemical reactions of oxidative stress that are being discussed here.

Now that information about the mechanisms of oxidative stress are amply available, It is time to start recalling the defensive part of the equation and to reiterate some of the many notable antioxidants that exist.  These anti-oxidants form the basis for one of the primary mitigating strategies under consideration to reduce oxidative stress. Once we know the source of a problem and its likely impacts, we are in a much better position to make headway in solving it.  This will be the case in terms of oxidative stress, and for other problems as well.

Returning to Robbins81 where the question was posed most directly, “Once free radicals are formed, how does the body get rid of them?”

and he answers equally succinctly, with one very important addition in this round of the research:

“There are several systems that contribute to termination of inactivation of free radical reactions.  These include:

1. ..Antioxidants [e.g., vitamins, glutathione, cysteine, transferrin]

2. ..Enzymes [superoxide dismutase, catalase]

3. ..Glutathione peroxidase” [which catalyzes reduced glutathione]

A definite pathway for research and consultation with health professionals has been charted here for anyone that cares to regard this information.  I would encourage you to consider it and evaluate it accordingly.

Let’s provide a specific example of what the oxidation process entails, along with  important definition of what an oxidant is.  An oxidant is known by several different names, all of which are the same thing, including, oxidizing agent, oxidant, free radical, or oxidizer.  An oxidant, or free radical, by definition, is “any species that contains one or more unpaired electrons occupying an atomic or molecular orbital by itself.82”  An oxidizer will essentially aggressively seek an electron from another species to form a bond with another atom or structure.

It is insightful to start the study by looking at oxygen itself, a major source of oxidation in its own right.  The bonding between oxygen atoms is a fascinating case that defies conventional interpretations, and further examination will show that oxygen itself is a radical with two unpaired electrons, and it is therefore known as a diradical.  This explains some of the reactivity characteristics of oxygen as we observe it, along with the interesting properties of paramagnetism (as can be shown with liquid oxygen experiments).  Oxygen in the free state that we breath (O2) has the following Lewis structure83, 84, 85, 86:

The diradical nature of oxygen, showing the two lone electrons of oxygen.  The special reactivity of oxygen can be understood more readily with this interpretation and understanding of oxygen bonding.

We are now in a better position to understand the sequence of free radical formation from oxygen as it forms within the body.  In healthy cellular metabolism, roughly 98% of oxygen is converted to water with the remaining 2% involving free radical production87, and Cadenas shows us a  sequential pathway that can take place, with the appearance of intermediate free radicals along the way ( superoxide anion and they hydroxyl radical)88:

Source : Enrique Cadenas, PhD

In more common language, we have the following description of the situation89:

“..oxidants or free radicals are the major cause of over a hundred human diseases. The process of ageing is also hastened by the onslaught of oxidants in the body. Oxidants are normally produced during healthy cellular metabolism, wherein 98 per cent of the oxygen consumed by a cell is converted to water. The remaining one to two per cent of the unutilised oxygen is free to escape as free radicals. Free radicals or oxidants are molecules containing single unpaired electrons, and are on the lookout for electrons to pair up. Examples of oxidants are superoxide anion, hydroxy one radical, reactive oxygen species like peroxides, hydroxides and singlet oxygen.”

The emphasis upon oxidative stress being an imbalance in the equation above is described again here, again in more generalized terms90:

“When the body’s antioxidative defences are inadequate, or when the supply of nutritional antioxidants is unreliable, or when the oxidant attacks are consistently alarming, the state of balance is tilted from a state of health to a state of slow degeneration.”

With this increased understanding of the route of oxidation within the body, let us return to the topic of countermeasures to oxidative stress.  Fortunately, understanding the nature of the problem does place in a stronger position to pursue countermeasures.  The recurring theme of the role of antioxidants is quite evident in the literature and health related papers available to us all; we simply must avail ourselves to them.  Again,  methods of mitigation are clearly portrayed in the Pharmaceutical Field article:91

“Over the years of evolution the human body has developed a whole arsenal of antioxidative enzyme systems and vitamins for its protection. Antioxidant systems of the body are critically dependent upon external dietary sources. What are these exogenous antioxidants and where are they found?

Natural Antioxidants To The Rescue
The vitamins particularly vitamin A in the form of beta-carotene and other carotenoids, vitamin C or ascorbic acid, and vitamin E as tocopherols and tocotrienols function as independently active natural dietary antioxidants. Minerals are the other dietary antioxidants that are critical to the activation of vital antioxidant enzyme systems in the body. Selenium is required for the antioxidant activity of the enzyme glutathione peroxidase. Zinc is essential for the activity of at least 90 enzymes including the antioxidant enzymes catalase and superoxide dismutase. Copper and manganese are also needed for superoxide dismutase activity.

Vitamin A and its polymers are available from brightly coloured vegetables and fruits such as carrots, apricots, dark green leafy vegetables like spinach, red, yellow and green peppers, sweet potatoes, and blue-green algae. Vitamin C is obtained from lemons, limes and other citrus and sour fruits. Vitamin E is found in nuts, whole grains, vegetable oils and to some extent in fruits and vegetables. In general, minerals are available naturally from fruits, nuts and lentils, whole cooked and germinating grains, shell-fish, vegetables and many others. Many other naturally occurring antioxidants that have been studied are pycnogenol from pine bark, grape seeds and red wine, lycopenes from tomatoes and beets, and coenzyme Q10 from red lean meat and blue-green algae. Garlic, tea and blueberries are also rich in natural antioxidants.

Supplementation of these dietary antioxidants in the right concentrations is important for protection against disease and premature ageing. Nutrition, like all sciences is constantly changing. Vitamins, minerals and other nutrients are no more ‘boring’ or old fashioned in the public consciousness. They have now been proven to act as antioxidants and protect against illnesses, repair tissues, and safeguard against the daily stresses of pollution and lifestyle. All of these substances are useful since they act as antioxidants at different levels and with different modes of actions. Consumption of these natural antioxidants through natural foods or commercially available nutraceutical or nutritional supplements will help in retarding the ageing process and increasing life spans, preventing and / or reducing the intensities of diseases like diabetes, artherosclerotic heart disease, cancer, arthritis, skin diseases, eye disorders and many other ailments.”

We continue to consolidate and extend our arsenal against oxidative stress, this time with a short presentation from the University of Colorado.  In the paper entitled “Free Radicals and Reactive Oxygen”, we find a helpful section at the tail of the article.  Two different classes of antioxidants are presented in this approach, those that are enzymatic in nature and those that are non-enzymatic.  More explicitly, the section of interest is as follows:

Mechanisms for Protection Against Radicals

Life on Earth evolved in the presence of oxygen, and necessarily adapted by evolution of a large battery of antioxidant systems. Some of these antioxidant molecules are present in all life forms examined, from bacteria to mammals, indicating their appearance early in the history of life.

Many antioxidants work by transiently becoming radicals themselves. These molecules are usually part of a larger network of cooperating antioxidants that end up regenerating the original antioxidant. For example, vitamin E becomes a radical, but is regenerated through the activity of the antioxidants vitamin C and glutathione.

Enzymatic Antioxidants

Three groups of enzymes play significant roles in protecting cells from oxidant stress:

Superoxide dismutases (SOD) are enzymes that catalyze the conversion of two superoxides into hydrogen peroxide and oxygen. The benefit here is that hydrogen peroxide is substantially less toxic that superoxide. SOD accelerates this detoxifying reaction roughly 10,000-fold over the non-catalyzed reaction.

SODs are metal-containing enzymes that depend on a bound manganese, copper or zinc for their antioxidant activity. In mammals, the manganese-containing enzyme is most abundant in mitochondria, while the zinc or copper forms predominant in cytoplasm. Interestingly, SODs are inducible enzymes – exposure of bacteria or vertebrate cells to higher concentrations of oxygen results in rapid increases in the concentration of SOD.

Catalase is found in peroxisomes in eucaryotic cells. It degrades hydrogen peroxide to water and oxygen, and hence finishes the detoxification reaction started by SOD.

Glutathione peroxidase is a group of enzymes, the most abundant of which contain selenium. These enzymes, like catalase, degrade hydrogen peroxide. They also reduce organic peroxides to alcohols, providing another route for eliminating toxic oxidants.

In addition to these enzymes, glutathione transferase, ceruloplasmin, hemoxygenase and possibly several other enzymes may participate in enzymatic control of oxygen radicals and their products.

Non-enzymatic Antioxidants

Three non-enzymatic antioxidants of particular importance are:

Vitamin E is the major lipid-soluble antioxidant, and plays a vital role in protecting membranes from oxidative damage. Its primary activity is to trap peroxy radicals in cellular membranes.

Vitamin C or ascorbic acid is a water-soluble antioxidant that can reduce radicals from a variety of sources. It also appears to participate in recycling vitamin E radicals. Interestingly, vitamin C also functions as a pro-oxidant under certain circumstances.

Glutathione may well be the most important intracellular defense against damage by reactive oxygen species. It is a tripeptide (glutamyl-cysteinyl-glycine). The cysteine provides an exposed free sulphydryl group (SH) that is very reactive, providing an abundant target for radical attack. Reaction with radicals oxidizes glutathione, but the reduced form is regenerated in a redox cycle involving glutathione reductase and the electron acceptor NADPH.

In addition to these “big three”, there are numerous small molecules that function as antioxidants. Examples include bilrubin, uric acid, flavonoids and carotenoids.

Readers may notice the level of overlap and correspondence that is now becoming evident in the specific compounds and substances that are regarded as highly effective antioxidants.  One may refer to the previous section from the pathology textbook that emphasized the role of antioxidants, superoxide dismutase (SOD), catalase and glutathione peroxidase to become aware of certain standards that have evolved in the oxidative stress research.  The special emphasis upon glutathione should also be noted, to the effect that93:

Glutathione may well be the most important cellular defense against damage by reactive oxygen species [free radicals]“.

Continuing the discussion on the importance of glutathione as an antioxidant, it is highly relevant to again recall the previous research paper entitled, “Morgellons : The Breaking of Bonds and the Reduction of Iron” from November of 201294.  This paper chronicles in depth research that describes the important role that glutathione is anticipated to assume in the mitigation of the Morgellons condition.  There are strong conclusions arrived at within this report, particularly those that concern the ability of glutathione to break down bonds in the identified proteinaceous structures, as well as  the ability of glutathione to reduce the oxidation state of iron.  It is thought that it may be highly beneficial to review the research presented in that earlier paper, as the proposals mentioned are now only further corroborated with the current research.  The link to this paper is presented immediately below:

Morgellons : The Breaking of Bonds and the Reduction of Iron

It may also be worthwhile to become familiar with an independent physician’s evaluations of the Morgellons issue and to take note of the acknowledgement of the prospects for glutathione benefits within that same paper95:  

Morgellon’s : The Role of Atmospheric Aerosolized Biological Nano-Particulates

A few other points related to the glutathione issue bear repetition within this current collection.  It has been described in earlier papers that glutathione is another one of the cases where direct supplementation may be of little value.  If we suppose that a body is lacking in a particular compound, substance, or enzyme, for example, a common instinctive reaction by many is that somehow it should simply be taken as a “supplement” to fulfill that deficiency.  This approach can be both unwise and foolhardy as our previous discussion on iron substantiates.  When information becomes available, it is of little value unless it has been interpreted properly and comprehensively.  It is another of the many reasons that professional health and medical counsel is to be sought and why education must be a lifelong pursuit.  There are risks in assuming that we know more than we do.  In that discussion, it was communicated that direct ingestion of glutathione appears to be of marginal value in human health.  The emphasis in glutathione production within the body appears to revolve heavily around the precursor biochemistry of glutathione, more than with glutathione directly.  The role of N-acetyl cysteine (NAC) has already been discussed in that regard in the previous papers mentioned.  It may be wise to become familiar with that the role of “precursors”, especially as they relate to the glutathione issue.  Over simplification of a problem and the seeking of immediate rewards without proper understanding and comprehension can have their own price in our lives.  The case for immediate and intensive participation by the health and medical communities to solve the health problems before us is patent.

Another topic of developing interest, especially in light of the current research findings, is the role that glutathione may assume in combating neural disorders, such as Parkinson’s Disease.  We are forced to consider the prospect of neural toxins (e.g., oxydopamine related compounds or structures) as being a potential component of the biological filament growth form.  This discussion has already taken place within this paper to some extent.  What is of interest here is to reacquaint ourselves with an introductory library of media on the glutathione issue, as also available in the earlier paper referenced96.


Dr. Oz
Glutathione – Master Antioxidant
(3 min)

Dr. Mark Hyman
Glutathione – The Mother of all Antioxidants
(10 min)

Dr. Don Colbert
Glutathion – The Master Antioxidant
Webinar Presentation (1 hr)

(No endorsements of products or services to be implied or stated herein)

Dr. David Perlmutter
Glutathion Therapy – Part I (2 min)

Dr. David Perlmutter
Glutathion Therapy – Part II (5 min)

(It may be of benefit to research additional presentations by these and other speakers on the issues of
glutathione, oxidative stress, chronic diseases and neuro-degenerative conditions)

An accessible and relatively inexpensive test (~$20) is available to test for oxidative stress in the body; this appears to be a highly valuable piece of information to assess with respect to the impact of the Morgellons condition and health in general.  A body of information at an anonymous level is available to this researcher and it does indicate that oxidative stress may be an especially important factor, as the research also shows in numerous and substantial ways.  The details of this colorimetric test are available at the manufacturer’s site96b and it may be found through numerous sources available to the public96c.  An example of a urine test result for one individual is shown below:

An example of the Oxidata(TM) test for oxidative stress and free radical production.  This test result indicates a high level of oxidative stress for this individual.



The following topic is deserving of more consideration in the future, but the relationships between antioxidiants, minerals and enzymes has been made more than once along this journey of discovery.  As one pharmacist relates (now from a perspective which emphasizes nutrition), speaking of reactions that involve antioxidants96d:


Most of these reactions need something called an enzyme to make them work. And many of these enzymes are actually antioxidants themselves- your body even makes them- that’s how important antioxidants are! Many minerals are vital parts of these reactions too, even though they’re not antioxidants themselves (so they’re equally important to have). These include selenium, manganese, copper and zinc.”


Clearly, there is more research and work to do, but the point has been made, and I suspect that it is an important one.


The next impact upon health that we transition to is that of excessive acidity, or acidosis.  There is significant evidence from the research of record to implicate a serious acidic component to the Morgellons condition.  The effects of excessive acidity in the body have been previously discussed, including demineralization, low energy, dental decay, weak immune system, chronic digestive problems, joint pains, bacterial and fungal infections, and many others.  Please review that section of this paper to recall the numerous and significant health effects that can accrue from over-acidity within the body.  Our desire here is to suggest what means might exist to counter the many problems are know the result from acidosis, and to suggest means by which extent of the problems might be monitored.

Researching the available literature, it is apparent that there is a fair amount of controversy regarding the strategies to counter the effects of excessive acidity.  There are individuals that claim that eating certain food groups are effective at changing the acid state.  There are individuals that claim that drinking water that is alkalized, often by various devices or with additives to the water, will result in beneficial effects.  There are individuals that claim that testing the pH of either urine or saliva is representative of the body chemistry.  There are individuals that will attempt to refute all of the above claims.  This section of the paper is neither to advocate or to dismiss potential methods that be beneficial; it is to increase awareness of the importance of the issue and to provide a modicum of education to point the reader to various possibilities for further research, advice or action.  The process of becoming aware of an idea or method does not imply or state endorsement, agreement or disagreement for that matter; it is to inform us of choices and research ideas.  What is clear is that a fair amount of controversy exists on this particular subject; usually in such cases there is an abundance of misinformation or disinformation (intentional or otherwise) that must be sorted through.  The profit motive of advocating certain and particular strategies, means, products and devices must also be considered in this regard.  

One method to approach this problem is to focus, at an introductory level,  on the medical condition of acidosis and to learn what are the identifying characteristics of that problem.  The term itself is usually used in a strict medical sense applying to reduced pH of the blood, however, it is also sometimes used to express generalized excess acidity at the cellular and tissue level.  Acidosis in the strictest sense of the term may well be a medical emergency, but we can use a study of that condition to our advantage to understand what systems of the body are being most seriously impacted.  It may then be  considered from that point on as a matter of degree as to how much the body may be impacted by excess acidity and to what extent.

We can start with the definition of acidosis itself.  Acidosis is an “increased acidity in the blood and other body tissue.  If not further qualified, it usually refers to acidity of the blood plasma”97.  Note here that there is no requirement from the onset to restrict our discussion to the issue of blood only, as it is not required by definition.  The measurement of blood acidity (pH) is not a common affair for the majority of us, and we prefer to not restrict our methods of measurement to that method alone.  Another very important statement within this same article to recognize is that “the rate of cellular metabolic activity affects and, at the same time, is affected by pH of the body fluids”98.  We will keep this statement close at hand, as we shall see that the issue of cellular metabolism will be at the heart of excess acidity within the body.

We can once again see that we are in no way restricted to the consideration of blood alone when we are dealing with the determination of acidity within the body.  Measurement of additional body fluids, such as saliva and urine, already appear to be reasonable to consider in our scope of acidity assessment, especially in a relative sense.  It is also a fact that the pH of urine is regularly used as a diagnostic aid in the medical professions.  Low pH values (i.e., high acid) of urine are indeed indicative of acidic conditions within the body, especially for those at risk of producing urinary stones99.  The measurement of the pH of urine does indeed appear to be a viable point of measurement for acidic conditions within the body.  One might also presume that such measurements could also be useful in a relative sense, i.e.,  to indicate changes of acidity within the body over a period of time.  

Before seeking out the root causes of acidosis, it is worthwhile to mention that acidosis comes in two primary forms, metabolic acidosis and respiratory acidosis.  Metabolic acidosis can result from the increased production of metabolic acids (please recall the discussion of organic acids earlier in this paper and the relationship to the carboxylic acid functional group) and kidney disturbances that excrete excess acids.  Lactic acidosis is a form of metabolic acidosis and it is characterized by low pH in the body tissues and blood.  Respiratory acidosis results from a buildup of carbon dioxide in the blood.  

An investigation into the research literature reveals two strong recurring themes as the basis and cause for acidosis.  The first of these will center on the issue of incomplete metabolism under conditions of reduced  oxygen and the second will involve the depletion of minerals.  We will now begin to document these important threads which immediately tie in with the leading statement that we called attention to:

the rate of cellular metabolic activity affects and, at the same time, is affected by pH of the body fluids

We refer to Dr. Michael Lam, once again, for a more lay interpretation of the importance of pH to body chemistry and for important sources of acid increase within the body.  Dr. Lam will also reveal to us the primary mechanisms by which the body compensates for this change.  Furthermore, Dr. Lam will make the case in his article100 that diet, in addition to other measures, is indeed a significant factor in affecting a change in acidity within the body.  This will come as no surprise as we investigate further the root causes of acidosis.

“One of the key determinants of the speed of aging and onset of degenerative diseases is the internal biochemistry and terrain of the body.  Internal biochemistry is best measured and discussed in terms of the pH.”

“The term acidosis is relative and only meant to convey a shift in total body chemistry towards the acidic direction.”

The principal sources of acid buildup are:

1.) The metabolism and/or incomplete breakdown (oxidation) of foodstuffs or metabolic “waste” produced as a by-product of cellular activity. During normal cellular respiration and energy production , acids as produced as part or “waste” products. These acid must be “balanced”, neutralized, or removed by the body’s buffering and detoxification systems through the kidneys, lungs, liver, and blood.

2.) The consumption of acid present in the food, air, and water supply. Nitrogen emissions from automobiles and industrial plants, food dyes, sprays, waxes, preservatives, additives, artificial sweeteners, fertilizers, water pollutants, and even chloride and fluoride in tap water are just some of the highly acidic chemicals are ingested by millions everyday.

How does the body overcome the acidity?

The body undergoes an natural and ongoing balancing act constantly. Underlying regulatory forces work continually to balance an acidic body chemistry to remove excess acid and return the body to a more neutral state.

These internal buffering mechanisms include:

a. The production of bicarbonate from the organs and cells of the body.

b. The removal of minerals such as calcium from bones to be used as buffering agent to neutralize the acid. This is one of the leading causes of osteoporosis.

c. The blowing off CO2 or carbon dioxide from the lungs. Carbon dioxide is an acid. It leads to symptoms of shallow breathing and hyperventilation.

d. The release of alkaline bile from the liver and alkaline digestive secretions from the pancreas and the retention of sodium from the kidneys in response to the secretion of the hormone Aldosterone.   Aldosterone is produced from adrenal gland, and stimulation of this gland leads to the feeling of internal “stress”.

For those seeking a somewhat more detailed explanation of how the body compensates for an imbalance in pH, it is instructive to examine the medical model approach.  In the paper entitled “Acid Base Balance in Critical Care Medicine101“, we find a modeling process that is applied to this problem that further confirms the statements in lay language by Dr. Lam above.  This model introduces the balance that occurs in the body extracellular fluid between positive and negative ions, primarily that of sodium, potassium, calcium and magnesium on the positive side and the chloride ion on the negative side (i.e., Strong Ion Difference).  Furthermore, it will be stated that a decrease in these positive ions will increase the hydrogen ion concentration (the very definition of an acid) through the buffering system in the body, resulting in acidosis.  

This modeling process is essentially equivalent to what has been stated by Dr. Lam, i.e., demineralization will accompany acidity within the body.  

Acid-base chemistry in the body can become a complex affair, and a detailed examination of the situation, factors and chemistry can be found at Dr. Grogono’s site entitled “Acid-Base Tutorial102“. A good introduction to acid-base chemistry is provided at the onset, where the two essential factors are described as follows:

“The Bird’s Eye-View, Two Components:

Respiratory: When breathing is inadequate carbon dioxide (respiratory acid) accumulates. The extra CO2 molecules combine with water to form carbonic acid which contributes to an acid pH. The treatment, if all else fails, is to lower the PCO2 by breathing for the patient using a ventilator.

Metabolic: When normal metabolism is impaired – acid forms, e.g., poor blood supply stops oxidative metabolism and lactic acid forms. This acid is not respiratory so, by definition, it is “metabolic acid.” If severe, the patient may be in shock and require treatment, possibly by neutralizing this excess acid with bicarbonate, possibly by allowing time for excretion/metabolism.”

As we continue to strike toward the heart of acidosis, at least from the more critical medical emergency perspective, one cannot help but notice that efficient aerobic respiration, complete metabolism and the lack of oxidative stress are at the absolute core of the issue.  These issues have emerged time and time again within this current research, and it would be foolhardy to ignore this deep-seated theme at this point.  In addition, we have learned that demineralization of the body (e.g., degradation of bone and teeth as examples) are expected to occur as a result of an acidic condition because of the body’s natural buffering systems that attempt to maintain ionic balance within the blood and body fluids.

The topic of excess acidity was first posited several years ago, in the paper (2010) entitled, Morgellons : A Discovery and a Proposal103, where attention was called to the following:

“In the culture environment, it has been established that the organism(s) flourish within an acidic environment.  In addition, it has also been stated in earlier reports that many biochemical reactions only take place within a narrow pH [acid or alkaline] range.  Therefore, one of the first strategies to consider is to change the acidity or alkalinity of the growth environment and see if progress results.  What has been observed in the cultures thus far is that an increase to the alkaline side does indeed appear to inhibit the growth of the culture.”

In a succeeding paper (2010) we find the following conclusions that were presented104:


“The growth of the bacterial-like organisms that appear to be at the foundation of the so-called Morgellons condition has been positively inhibited…The basic strategy that has been adopted is a transformation of the growth environment to a more alkaline condition along with adding specific antioxidants that are directed toward the scavenging of the hydroxyl radical.

We turn now to an additional important means to alkalize the body, that of bile production by the liver.

Attention was called  in 2011 to the role of bile as one of several mitigation strategies listed in the paper,  Morgellons : A Thesis105(2011):

…”Improving the flow of bile in the system to further alkalize the body and aid the digestive system. The liver, the gall bladder and the bile duct play an extremely important role in alkalizing the digestive tract.  For those that demonstrate a persistent acidic condition within the body it may be beneficial to learn of the importance of bile production and its alkalizing function.  

An acidic condition can easily be created with a blockage of the bile duct, as the bile is the alkalizing agent within the intestine.  Gall bladder removal and gall stones appear to be a frequent occurrence; this would suggest that overloads of toxicity to the liver could well be at the root of this problem.  Non-invasive methods of breaking down gall stones (conglomeration of bile) are available to consider, such as Chanca Piedra (breakstone).  If the bile flow is restricted, an acidic condition within the body is expected to exist.  Knowledge of the physiology of the liver, gall bladder, bile duct and its relationship to digestion may be beneficial in mitigating the consequences of acidity within the body and digestive system.”

Furthermore, the reader was introduced at that same time to an educational video on the relationships between the liver, bile production, acidity, alkalinity and immunity was made available at the following site:

Video Series: Liver, Gall Bladder and Bile Duct Physiology

(No endorsements of products or services to be implied or stated herein)


There are recent observations of liver tissue that are important to be briefly introduced at this time; the subject will be discussed in more detail at a later date.  If the body is unable to process the toxic load placed upon the digestive system, there will be an accumulation of these toxins within the body.  The function of the liver is manifold, and detoxification and waste removal is foremost on that list.  The liver is also responsible for protein synthesis, the breakdown of fats with the production of bile, glycogen storage, decomposition of red blood cells, iron regulation, and many others.  We only have one liver and we cannot afford to have a serious problem with it.

One of the major problems with the liver (of increasing incidence) is the accumulation of fatty tissue within the liver.  It is estimated that more than 1/3 of the population now suffers from fatty liver disease that is unrelated to excess alcohol use.  The net impact from the accumulation of these toxins  is an enlarged and fatty liver.  If the liver is unable to process the toxic overload, fat cells with the toxins will accumulate and be stored within the liver.  It is potentially a serious situation and one that is difficult to reverse quickly; weight gain is often associated with the condition.  What follows is a photographic comparison of a healthy and a fatty liver:

source :

From visual impressions alone, it is clear that this condition is not a healthy one.  It is reasonable to conclude that the functioning of the liver is seriously impaired with this condition.  We can also find examples of what the fatty liver looks like under the microscope, also in comparison to healthy liver tissue:

Comparison of normal liver tissue(left) and fatty liver tissue (right)
source :

Recent observations of calf liver under the microscope show this condition of fatty issue existing.  There are two concerns present from this initial observation:

Appearance of significant fatty liver tissue within a calf liver recently analyzed.
Sub-micron bacterial-like structures (identical in size and shape to those studied extensively on this site)
are abundant within the fatty cells.  Magnification approx. 8000x.

1. The animal is young, and therefore excess fatty tissue would not be anticipated at this stage of growth.

2.  The fat cells are enclosing large numbers of what appear to match (identical in size and geometry) the sub-micron, bacterial-like structures that are the subject of much scrutiny within the research of this site and this current paper.  

It is reasonable to surmise that the abundant presence of the encapsulating fat cells represents a toxic-overload response by the liver in the young animal.  Other issues of equal and concern arise from this recent observation; this research is to be presented at a later date.

For numerous reasons, there is a legitimate case for concern about the impact of the Morgellons condition upon the functioning of the liver; this includes potential toxic overload, fatty tissue development and the prospect for an enlarged liver that results.  If such proves to be the case, there is an obvious need for consideration of liver detoxification strategies to be incorporated within this report.

Although he have now forged through some of the controversies regarding acid-base imbalances, it is certain that some shall remain after this paper is complete.  The issue of drinking water that has been “alkalized” must be given mention, however unappealing the circumstances may be to certain parties along with their particular knowledge base.  There are those that advocate that certain alterations of water, either chemically or with certain devices and technologies, will be sufficient to address the acid-base imbalances under study here.  I do not find such arguments, thus far, generally sufficient to justify such conclusions at this point.  It is evident from the work at hand that sufficient oxygen available at the cellular level, thorough aerobic metabolism, reduction of excess carbon dioxide, mineral balance, diet (especially as it relates to mineral intake) and the alkalizing processes of the body (e.g., bile production and flow) are at helm of acid-base balances within body and health.  The argument for a modification of the “water molecule” (under question in its own right) to account for and compensate for the complex systems mentioned above appears that it may be lacking in the necessary substance of this problem.  Whether one “agrees” or not with the following information from Dr. Lawrence Wilson on the topic of “alkaline” water, it behooves us to become familiar with the arguments put forth106:

“The pH balance of the body is very important, and most people’s bodies are too acidic at the cellular level.  It does not matter if the saliva, urine or other fluids test alkaline.  In almost all cases, the body cells, which is the site of metabolism, are too acidic.  This predisposes one to many metabolic imbalances and diseases including cancer.  The rationale for drinking alkaline water is that it will correct this important physiological imbalance.

Problems with this rationale for alkaline water.  The main problems with this theory are

1. The real cause of excess acidity at the cellular level is a deficiency of what are called the alkalinizing or alkaline reserve minerals.  These come from what one was born with, and from the diet.  If one lives a stressful life, one also depletes these quickly.  They include calcium, magnesium, zinc, selenium, and a few others.

Unfortunately, drinking artificially alkalinized water does little or nothing to replace these vital minerals.  In fact, it may deplete them for unusual reasons.  It may make the body think it is alkaline, so the body does not need to hold on to its alkaline reserve minerals as much, and it eliminates some of them, making the person even more deficient.  

2. Water from alkaline water machines replaces the vital minerals with a little cadmium, lead, arsenic and other toxic metals found in tap water and not filtered by any carbon filters that I am aware of.  Some filtering systems claim to filter out toxic metals, but I have not observed this in practice.  Those filters that I have seen that are said to remove a lot of toxic metals tend to damage the water even worse.  Reverse osmosis is an example of this type, along with KDF and other types of “advanced” filtration media.

3. In addition, the alkaline water machines also replace the good minerals with a little platinum and titanium found in the plates that the water passes over to make it alkaline.  These are both supremely toxic metals, especially platinum.  In addition, I have observed slightly higher levels of nickel in those who use alkaline water machines for several years.  

The nickel is probably leached from the stainless steel in the machine, or perhaps from a nickel-plated machine part.  Nickel is a deadly toxic metal.  The alkalinity of the water may cause a little to be leached out of the machine parts.

4. Carbon filtration also does not remove enough of the toxic chemicals in the water, so one is also getting a dose of chlorine, fluorides, aluminum, copper, residues of medical drugs in many areas, pesticides and more.

5. As a result, alkaline water machines do not really balance the body’s pH, although they will change it a little, giving some people the impression they are getting well when, in fact, they are becoming more ill. The only way to truly balance the body is to replenish the alkaline reserve minerals.  To do this, one must eat a lot of cooked vegetables.  The cooked vegetables, and perhaps some mineral supplements, when carefully chosen such as kelp, can and do supply the alkaline reserve minerals.  Good quality, natural spring water also supplies some alkaline minerals, as does good quality sea salt.  Using these on a daily basis, the body can be slowly remineralized.  This is the way to do it, not drinking artificially alkalinized water.”

We can once again see the emphasis upon the alkaline reserve minerals as a major pathway toward the restoration of the acid-base imbalance, with an emphasis upon diet to accomplish this.  The verdict on exotic or expensive technologies to alter the “state” of water is left to the reader to investigate further;  I would only encourage that the study be rooted in chemistry, biochemistry and physics as opposed to promotional claims.   At this point of study the causes of and factors affecting increased acidity, from numerous and varied sources, parallel the summary given by Dr. Lam to us at the onset (please review) remarkably well.  These include incomplete metabolic breakdown of foods and nutrients, the lack of availability of sufficient alkaline reserves, the ingestion of acidic toxins or foodstuffs into the body, carbon dioxide imbalances and the failure of the bile system to adequately alkalize the intestinal tract.  The road to recovery from the impact of such damage is to reverse the courses above, i.e., increase the efficiency of the oxidation of fuel, assure adequate oxygen in a form that the body can actually use, intake sufficient alkalizing minerals (such as calcium, magnesium, etc.) and improve the flow of bile and improve the digestive processes in general.  It is obviously a tall order, but courses of action are readily available to all of us.  Consultations with health practitioners about the sensibility or validity of the information being relayed here is a good start in the process.  Supporting this process with your own studies and research on the matter can only be of further benefit.

For those that continue to profess that what you consume does not materially affect your body chemistry, or for that matter, the acid-alkaline imbalance in general, let us cite a more traditional example from the American Journal of Clinical Nutrition on the subject of diet, pH and oral health.  It states clearly that what we eat is not a neutral affair107:

“..Diet affects the integrity of the teeth; quantity, pH, and composition of the saliva, and plaque pH.  Sugars and other fermentable carbohydrates..provide substrate for the actions of oral bacteria, which in turn lower plaque and salivary pH.  The resultant action is the beginning of tooth demineralization.”

Readers may once again be struck by the association between acidity and demineralization; the relationships between diet, body chemistry, acidity and alkalinity are all too apparent in the literature.

The preceding section serves as a welcome segue into the realm of what may be rather unsung heroes; those that have devoted themselves to health, nutrition and “functional medicine”.  Many of us look to a particular type of “doctor” to “heal” an ailment or disease, but those that study the role of nutrition in promoting health and those that study health in a more holistic sense are likely our true and best allies.  There are many individuals that have studied extensively the relationships between oxidative stress and acidity, for example, with nutrition and the body systems in an integrative sense.  It is wise for us to avail ourselves of their talent and knowledge, as opposed to only seeking a particular “cure” to a “particular ailment”, including that of “Morgellons”.

If we now open our discussion to include the counsel of those that study nutrition as a lifelong passion and its role in our health, the association between health and the acid-alkaline balance is prominent within the literature.  For those that continue to advocate that saliva and urine pH have no real value in the assessment process, it may be prudent to become familiar with a portion of the following discussion.  For those that seek out the credentialing process, Dr. Biamonte is no lightweight in the profession of clinical nutrition.  One article worth studying in detail is entitled, “Urine and Saliva pH Testing”108 from the Biamonte Center for Clinical Nutrition.  A few excerpts are in order here, but it is advised to study the article in detail.  The acid-base balance discussion, the role of minerals (once again) in the process, and various simple testing procedures for both saliva and urine are worthy of your consideration.  Please conduct your own research with the critics as well and reach your own conclusions as to motives and intentions of various parties.  You may also wish to examine the documented effects of demineralization and destruction of teeth and bone documented earlier in this paper, as well as to study those that have suffered from these effects.  The mineral loss in these cases is clear and evident, and it is difficult to deny that the acid-base balance is an important part of the process.

In the meantime, let us proceed with some representative sections from the article:

“Simple tests of your saliva and urine that you can perform yourself can give you a good idea of the pH levels of your body…”

“Testing urine and saliva after sleeping at least five hours gives you an idea of how your body is operating. Urine pH tells of how your body is responding to the food your ate the day before. Saliva pH tells your how your body has accepted the past few weeks and months. If you have not been eating foods that contain alkalizing minerals, your body has adapted its function to keep pH of your blood and other vital fluids as correct as possible. It is often these long term adaptations that are necessary for survival- that eventually lead to symptoms of chronic degenerative diseases such as arthritis, osteoporosis, emphysema, or even cancer.”

“Alkalizing minerals are stored in many organs and tissues of the body. The liver is the greatest storehouse of sodium; the bones are the greatest storehouse of calcium. Yet these storehouses can be emptied if the minerals that are used can’t be replaced. The food you eat determines how well your reserves are replenished. Fresh fruits and vegetables contribute the usable alkalizing minerals you need to restock your alkaline reserve. When there are enough reserves to buffer the acid produced naturally by cellular activity saliva pH will register around 7.0. Readings of considerably lower or higher than 7.0 usually indicate that your buffering reserves have been depleted and your body is being forced to accommodate by other means.”

“The urine represents what we are eliminating, the saliva represents what we are keeping. The urine does not accurately represent the state of the body, but does represent what it is eliminating – ideally acidic wastes. The first morning saliva pH is the indicator of the state of the body: tissue, lymph, interstitial fluids and blood.”



This urine/saliva tests shows basically how many minerals are left in our bodies, i.e. what the MINERAL RESERVES of the body are and what we must do to remineralize it. This lays the foundation for any and all healing therapies.
* The test is simple:

All of the following pH tests should be done on same day.

1. Saliva test upon waking. First thing in the morning right when you get out of bed, lick and wet the MIDDLE BOX OF THE PH TEST STRIP. Note the color change and write down that pH number. Do this before brushing your teeth, drinking, smoking, or even thinking of eating any food. This pH should be 6.8.

2. Then test your second urine of the morning. The urine stored in your bladder during the night, that is ready to be eliminated when you get up, should be acid so you don’t want to test that. Drain your bladder in the morning, the last time you get up if you get up during the night and then see what that urine pH is. Again, record this number. This number should be the pH of your urine after you got rid of your acid load from the day before. The acids should be gone the second time you go to the bathroom so your urine pH should be around 6.8 also.

3. Eat breakfast, an apple will do, anything, and five minutes after breakfast check your saliva again. Write this number down also. This number should go up from what it was before you ate, the more the better.

4. Then check your urine pH between breakfast and lunch. . The pH should always be 7.0 to 8.5, a couple of hours after meals.

5. Then check your urine pH between lunch and dinner. The pH should always be 7.0 to 8.5, a couple of hours after meals.

These five tests show the following:

1. How well your digestive system dealt with what you ate the night before, i.e. the AM urine pH. These numbers may change from day to day depending on what you did eat the night before.

2. How well we treat ourselves in general, i.e. how “strong” the liver is. This is the AM saliva pH. This number shows the overall state of our health, the condition of the alkaline reserve of our bodies which reflects the diet we have eaten over the last months to years. This number stays rather constant and will only change after some work has been done in re-mineralizing the body. Pleomorphism and its changes can be viewed under the darkfield microscope, but the saliva pH shows what you will see.

Since the saliva pH is an indicator of intracellular pH, saliva pH readings should never be below the pH of the phosphate buffer system, 6.8. (see below). The most accurate reading of saliva pH is recorded immediately upon awakening–after sleeping at least five hours and before brushing the teeth. It is during sleep that the body removes waste and is in an anabolic state restoring and replenishing the body. If the patient has a saliva pH of 5.5 at this time and only 5.6 after eating, you know that this person has no alkaline reserve and that his body is devoid of the minerals necessary to process food properly–his body cannot adequately respond to the physiological crisis of handling food.

3. The pH of your saliva after you eat gives an indication of what the mineral reserves of your body are (the pH number should increase after you eat). The ideal saliva pH pattern is 6.8 on awakening, 7.0 before eating and 8.5 following breakfast.

4. The pH’s of the urine between meals should be kept in the basic range, pH 7.0 to 8.5. After one eats, the stomach generates the necessary acid to digest the food. While doing this, it also performs the opposite action, i.e. it makes an equivalent amount of base or baking soda, sodium bicarbonate, that is picked up by the blood stream and delivered to the alkaline glands of the body, the saliva, the pancreas and the liver. The maximum amount of base in the blood and therefore in the urine occurs one to two hours after you eat. The body fluids and therefore the urine is most acid at 2:00 A.M. (pH 5.0 to 6.8) in the morning (the base tide) and most alkaline at 2:00 P.M. (pH 7.0 to 8.5) in the afternoon (base flood).

Along the course of the article, Dr. Biamonte also introduces us to the “lemon-test”, a relatively simple test that can be used to give an indication of the available mineral reserves in the body.  The history of the test and its use extends well beyond any single practitioner, and it is also described in some detail by Dr. Dicken Weatherby in his book on functional medicine, “In Office Lab Testing : Functional Terrain Analysis109“.  Various examples of test results are described within this same book.  The origin of the test appears to reside with a Dr. Henry G. Bieler, MD.110, the well known author of “Food is Your Best Medicine”.

The introduction to the pH Saliva test, from
“In Office Lab Testing : Functional Terrain Analysis” by Dr. Dicken Weatherby

I have witnessed the administration of the test locally, and I find the results to be of much interest and expressive of variation between individuals.  The test is simple enough in principle and practice to monitor individually if desired, as in the following example with two separate individuals.  

The Acid-Lemon Test conducted by two separate individuals.  The individual on the right demonstrates a stronger decrease in pH over the time interval measured.  The reasoning behind this test concludes that the individual on the right is likely to have reduced mineral reserves available, and consequently a higher acid level may be anticipated within the body tissues.   The sharp rise in pH on the individual’s test to the left may apparently also reflect ammonia imbalances and is also worthy of further study.  Important nuances in the test do exist and they are worthy of further research;  Dr. Weatherby’s book may be helpful in this regard.

Additional simple tests for an acid-alkaline imbalance (i.e., breath holding test and respiratory rate test) are described in one of several of Dr. Dicken Weatherby’s books110b on the subject of functional medicine. 

Any readers with a further interest in these topics may wish to consult those that practice in the field of functional medicine, or as stated repeatedly, the health practitioners of choice.

A general introduction to the fundamental principles and philosophy of functional medicine is available courtesy of Dr. Mark Hyman:

Mark Hyman, M.D., Introduces Functional Medicine

Listen to a more extended discussion by Dr. Hyman on the state of health and Functional Medicine.

We can speak of such issues of oxygen, energy, oxidation, acidity and pH at length, but me must move on to make further progress.  For those that continue to profess that there are no relationships of consequence between these factors, or little that can be done about them, let us make a more blunt parting observation as to what happens in the body when we die.  On the topic of acidosis (i.e., excessive acidity within the tissues), under the subtopic of associations,  we learn starkly that111:

Lactic acidosis is an underlying process of rigor mortis. Tissue in the muscles of the deceased carry out anaerobic metabolism in the absence of oxygen, using muscle glycogen as the energy source, and significant amounts of lactic acid are released into the muscle tissue. With depletion of muscle glycogen, the loss of ATP [i.e., energy production]causes the muscles to grow stiff, as the actin-myosin bonds cannot be released. (Rigor is later resolved by enzymatic breakdown of the myofibers.) In meat-producing animals, the post-mortem pH drop in muscle tissue contributes to meat quality (by influencing water retention, cutting color and texture of meat) and also contributes to food safety by inhibiting several acid-intolerant spoilage organisms that otherwise might proliferate, even at refrigerator temperature.”

It would seem as though there are obvious relationships that exist between acidity, oxygen, and energy production when we are dead. There is every reason to think that such relationhips exist while we live as well.  

One famous line from mutated history and the cinema is that, “Today is a good day to die…”  

Our alternative line for today (not quite so famous) is that, “It is a good time to talk about the thyroid.”  And so on we go…

We can now recall the importance of the thyroxine, the primary hormone of the thyroid:

“Thyroxine stimulates the production of oxygen in the body.  Thyroxine is directly related to carbohydrate metabolism, protein synthesis and breakdown.  Thyroxine stimulates the utilization of energy.  Thyroxine directly affects the basal metabolic rate.  Thyroxine stimulates the cells of the nervous system.  Thyroxine is used to maintain the state of the cardiovascular system.  Thyroxine stimulates the breakdown of fats.  Thyroxine stimulates normal growth and development.  Thyroxine stimulates the muscles to break down proteins.  The thyroid is, therefore, a master regulator of metabolism for the body and any interference in that functioning is inevitably and seriously detrimental to human health.”

We can see that the thyroid is the metabolic master of our system, and it is harder to get much closer to home than that.  We also have good reason to suspect that thryroid processes are being interfered with in conjunction with the Morgellons condition.  Our most fundamental indicator of this disturbance is that of body temperature.  There is good reason as well as evidence to show that the body temperature of the general population is operating frequently at a temperature less than normal.  The mantra of “98.6” that many of us grew up with may not exactly be quite so vocal these days, and the mystery of that silence is deserving of intensive study. 

We also have reason to consider interference from the standpoint of aromatic chemistry; this has been discussed at length earlier in this paper.  Essentially, the existence of aromatics along with amines is a perfect setup to initiate the halogenation of the aromatic structure.  Halogenation of an aromatic structure by the halogens foreign to the body, e.g., fluorine, chlorine and bromine, is also the perfect setup to interfere with thyroxine, or the thyroid itself.  

Third, we have a relationship of interference to consider between tyrosine (an amino acid), the thyroid (with thryoxine production) and dopamine (a neurotransmitter), as it has been discussed previously.  We will also revisit this topic when the subject of neural disruption is discussed later.  No matter which way go about it, we obviously have important issues at hand here, and metabolism and body temperature indicators are the heart of it. We will focus on this issue of body temperature, as it is direct and apparent, and it is easy to measure, and monitor for change.  It is a macro indicator that affects the entire body system.  Our Biochemistry is essentially non-functional without the proper conditions of temperature and pH in place (for ALL reactions), and we must never lose sight of this fundamental fact as we wade through this maze of complexity and interaction.

What does low body temperature mean, at the most fundamental level?  It means the body is not working up to speed; the engine is not running at the proper temperature.  If the engine does not run at the proper temperature we have incomplete combustion and less energy is produced.  In essence, the body is not working as it should, and it is definitely not firing on all cylinders.  In more conventional terms, an underactive thyroid is called hypothyroidism and the overactive thyroid is called hyperthyroidism.  The signs of research in place point quite strongly to the former in association with the Morgellons condition.

Let’s look at the connection between temperature, metabolism and the thryroid from several sources and in more detail: First, a direct statement of the relationship from a detailed source on medical testing112:

“There is a direct link between low body temperature and low thyroid function. In fact, one of the symptoms of hypothyroidism is the reduction in body temperature.”

In equal plainspeak, Dr. Rind introduces us to the importance of the relationship, as well as the role the adrenals have with respect to temperature variations113:

“If you’re not feeling quite up to par, take your temperature. Not to determine if you’ve got a fever – rather, temperatures reflect an individual’s metabolic energy state. The average daytime temperature of a healthy individual is 98.6 thus making 98.6 the optimal (as opposed to normal*) temperature. Lower than optimal temperatures reflect a lower than optimal metabolic state which is usually controlled by the thyroid mechanism. Wide variability of temperature reflects an unstable or fatigued adrenal system [please note this addition to our considerations -CEC]. Thus, on the road to health, one wants to go from low and/or unstable temperatures to 98.6 and stable if possible.”

Detailed information about a method to monitor your temperature and its variability is available on Dr. Rind’s site as well.  The awareness of the state of temperature in the body, its importance to efficient metabolism, and a system to track and monitor temperature on a regular basis may be a beneficial first step in becoming aware of the importance of thyroid functioning to good health.

Lastly, to cement the importance of the relationship of body temperature to thyroid functioning, Dr. Weatherby also describes a Body Basal Temperature Test114 and reiterates the primary point made:

“A reduced core body temperature is one of the hallmarks of thyroid hormone deficiency and hypothyroidism.”

The widespread reporting and observation of reduced body temperature amongst the general population , in addition those those more visibly suffering from the Morgellons’s condition, should make it apparent that hypothyroidism is a central topic of research here.  This paper can only hope to introduce the importance of this issue in this and future studies..

If we postulate that a state of hypothyroidism exists, i.e, a state of lowered metabolic rate associated with the lower body temperature cited above, what then are some of strategies offered by the health community to alter this situation?  It would certainly seem, then, that the cause of such a problem would need to be identified first.  We have certainly called attention in this paper to the possible role that the halogens might assume in such a case, and the interference that the toxic halogens can create.  An obvious first approach might be to reduce or eliminate the presence of toxic halogens within the body, and to avoid contact or ingestion of them.  Let us seek out how the health communities might react this to this potential problem.

If we begin by asking the question of how one would detoxify from an excess of halogens, especially that of fluoride and bromide, we are immediately led to an abundance of discussion related to iodine therapy.  The reasons for this have already been discussed, and these relate to the relative reactivity of the halogens and their competition of iodine within the thyroid.  We can repeat that relationship with the words, to start, from Dr. Mark Sircus :115

“It is well known that the toxic halides, fluoride and bromide, having structure similar to iodine, can competitively inhibit iodine absorption and binding in the body.”

We are also immediately led, therefore, to a strategy of great importance and interest, i.e., iodine therapy, or the intake of additional iodine into the body.  Expressed as follows by Dr. Sircus in conjunction with Dr. Gyula:

“Iodine intake immediately increases the excretion of bromide, fluoride, and some heavy metals including mercury and lead. Bromide and fluoride are not removed by any other chelator or detoxifying technique. Dr. Kenezy Gyula Korhaz states that iodine chelates heavy metals such as mercury, lead, cadmium and aluminum and halogens such as fluoride and bromide, thus decreasing their iodine inhibiting effects especially of the halogens.“I

It is more than explicit at this point that no medical advice is ever given or implied within these papers, however, information and education IS to be freely available to all.  It is clear from the literature and research that iodine supplementation in connection with thyroid performance is extensively discussed and employed.  The chemical and molecular rationale for that strategy has already been made clear within this paper; the details of consideration and application will be left to the reader.  The responsibility for education and professional consultation in any such matters is also equally obvious.

Examples of the need for education and consultation on the matter is apparent from the following two complicating factors:

1.  Another strategy, commonly employed, is that of prescribing an increase in the thyroid hormone (T4) itself to remedy hypothyroid (decreased thyroid function) imbalances.    In the book, Thyroid Balance, by Dr. Glenn Rothfeld, we read that:116

“Doctors typically prescribe a thyroid supplement -a drug that boosts the thyroid hormones in your system -to treat most thyroid imbalance.  This is a tried-and-true therapy that has been the standard for more than a century.  The earliest documented use of this therapy dates to 1891, when doctors started using ground thyroid gland tissue from sheep to treat severe hypothyroidism”

2.  Allergic reactions to iodine supplementation are known to exist.  The extent and reaction of an allergic reaction is certainly outside the scope of this article, but attention will at least be drawn to the matter.

3. Another question that can be asked, similar to those issues that were raised earlier with respect to deficiencies in iron, is whether or not we take care of a deficiency by simply adding more of  the same thing back into the system?  If we do not understand what is causing the deficiency of a particular substance to begin with, supplementing it with the same substance may be a completely futile exercise.  Hence the interest of “Thyroid Inhibition” increases, and consequently the interplay with iodine remains a focal point of the strategies discussed here.

4.  The relationship between adrenal performance (and cortisol levels) and thyroid function is also important to be aware of.  There is some information from the research of this Institute that the undue stresses on the adrenal glands may well be another point of serious research as it relates to the Morgellons condition.  There is an additional caution provided to us for the simplistic response of simply increasing the thyroid hormones with supplements:117

“Thus, it can be important for you and your doctor to rule out insufficient adrenal function before raising too high on natural dessicated thyroid or T3…”

Self-tests for adrenal function are subsequently described in this article, but the point is again made that thyroid hormone supplementation may be a diversionary exercise.

Education and research are the goals here, not therapy.  Education and research are obviously on the path toward therapy, and these are our pursuits.

While we are on the subject of self-tests, let us include another test, this time related to iodine deficiency.  There is an additional test entitled the Iodine Patch Test within Dr. Weatheryby’s book mentioned earlier118.    It is a simple test that monitors the fading of an iodine patch (2%) painted onto the skin over a 24 hour period.   As Dr. Weatherby describes,

“The Iodine Patch Test is an excellent test for assessing for iodine deficiency…Unfortunately, iodine deficiency is widespread because of the prevalence of chemicals such as chlorine, bromine and fluoride [note halogen emphasis – CEC] in our environment and water supply.  These chemicals will quickly deplete iodine from the body and interfere with iodine metabolism leading to a number of problems including hypothyroidism, lowered vitality, cognitive dysfunction, lowered immunity, and obesity.  The iodine patch test is an easy method of assessing your iodine levels.

Once again, we may ask, does this sound familiar, relevant and germane to the findings of this report?

Readers are referred to Dr. Weatherby and other sources for more particular details on the interpretation of the test results.  There are those who think that the iodine patch test is not reliable and therefore not useful; as such it exists in controversy amongst some practitioners.119  It would appear that the lower body temperature test is less so and it is simple in principle to comprehend.  Recall from earlier discussions that all biochemical reactions take place at a specific temperature and pH; alteration of either of these parameters will inevitably lead to impairment of some sort or fashion.

We start this by mentioning forms that are not advisable and that have varying levels of toxicity – conventional antiseptic iodines.  The first clue that such forms are not of benefit is the warning label, which will clearly state that this form is not to be used for internal purposes.  There are two forms described that are in common use:120, 121

1. Tincture of iodine – a mixture of elemental iodine and either potassium or sodium iodide, dissolved in ethanol and water  Denaturing of the alcohol is also know to be used in commercial tinctures.  A 2% free iodine solution contains about 1 mg of free iodine per drop.  Ethanol is poisonous in sufficient amounts and denatured ethanol is deliberately poisoned to prevent consumption.  Tincture solutions can vary between 2% – 7% in strength.

2. Povidone iodine is a mixture of PVP (polyvinylpyrrolidone) and elemental iodine.  It is soluble in both water and alcohols, and is more stable chemically than tincture of iodine.  The deposition of PVP in human tissues  reported in toxicology tests warrants abstention from use internally.122

We now transition to forms that are more suitable internally to the body (notwithstanding the prior caveats of potential allergic reactions, etc.).   A statement of additional risk factors associated with the ingestion of iodine are included from the following medical bulletin from the National Institutes of Health; all readers are advised to be aware of all information that is contained within this report.123

Medline Plus : Iodine :

Now that we have given due notice to the federal standards for recommended levels of iodine in the body, let us open up the discussion to various professionals that have devoted significant study to iodine as it relates to health.  It will be clear that the federal recommended levels are dramatically at odds with many serious research studies on the subject. For an extended discussion and debate between those at the forefront of iodine therapies (Abraham, Brownstein) and those advocating more restrictive conventional approaches (Gaby), please see the following paper:124

The Great Iodine Debate


The following media presentations are recommended as an introduction to the important role that sufficient iodine and iodide levels plays with in our health.  More extended discussions of the necessary levels of iodine in the body, the manufacture and storage of iodine, differences between iodine and iodine forms,  body capacity and removal of excess iodine, skin issues related to iodine deficiency, the damage and competition for iodine by the halogens, the dangers of the halogens with respect to modern diets, and improved brain functioning with appropriate iodine levels are all important topics that are covered in these presentations.  The reader is advised to become familiar with the material that follows.

(Here is a test for you: find the place in one of the videos where “RDA” is stated to stand for a “really dumb idea (sic?)”.)

Jorge Flechas, MD, on the topic of Iodine Sufficiency

Dr. Brownstein, MD, Iodine, the most misunderstood nutrient

Drs. Mercola & Brownstein, MD,
on the topic of Iodine Deficiency

(note the attention given to the bromine issue)

Dr. Tenpenny, on the topic of Iodine Deficiency
(Advanced Discussion)

We can see from the presentations by numerous doctors and extensive research that there is a strong case for the existence of increased levels of toxic halogens in the body (i.e., fluorine, chlorine and bromine) and for the competition that they exert upon iodine and the thyroid.  This case in in alignment with the spectral and biochemical analyses that are a core result of this paper.The symptoms of impaired thyroid function such as reduced body metabolism and energy production, lowered body temperature, skin complications, brain dysfunction, cancers and many other serious health issues are intimately related to iodine deficiency.  Iodine therapies are also offered as a significant prospect for improvement by these same doctors.  The case for the existence of the aromatic halogens in association with the Morgellons condition has also been made by this researcher through the use of infrared spectral analysis, with a particular interest in bromine substitutions.  It is also important to emphasize the major differences in the amounts of iodine that are necessary and utilized in the body compared to those identified in the federal standards; this difference ignores the prospect of increased competing halogen sources that may now have been introduced into the body.  This difference, even based upon conventional medical research of recent decades as outlined in the presentations above,  is on the order of 100 times.  Impairment of thyroid functioning and iodine supplementation therapies exist, therefore, as compelling and major topics of further research in the investigation of the Morgellons condition.

We now begin to close this chapter of research in the history of Carnicom Institute, and we depart (temporarily, of course) with a brief revisit to, and a discussion of, the neural disruption issue.  It is difficult to ‘rank’ the relative importance of the numerous issues that have evolved within this current research and their combination is devastating and ostracizing to far too many.  This level of harm and suffering is much greater than that which is currently acknowledged,  and many individuals deserve recognition for the battles they are fighting.  These  battles are often fought in solitude and they can be literally a fight for life itself.  We must offer our compassion, our care and our help in haste, as the frog pot continues to warm for most of us.

It is clear that cognitive functioning, concentration ability and mental acuity in general are companions of study here, and that they are closer to home than many of us would like to admit in our pursuit of improved health.

The technical and evidentiary argument for this situation has already been made in this report, and our question here is what can be offered as a prospect for improvement?  Certainly the first fact to recognize is that the broad health impacts that have been discussed here are usually related to one another, and it is simplistic to separate them as islands of trouble.  How can we possibly suspect a simple ‘cure’ to any demise of neural and cognitive functioning; in the majority of cases modern medicine is still in its infancy here.  Nonetheless, there are ALWAYS paths to pursue to improve the lot of us, and there are no exceptions here.

We may start with the glaring theme of oxidative stress, which is pervasive and illustrative of the connections between the topics of this report and those that are at the foundation of pathology.  This foundation (e.g., Robbins125) has already been discussed some time ago in a context that is much broader than the Morgellons issue by itself.  Is it any surprise when we learn, therefore, that:126

“Oxidative stress plays a pivotal role in the pathogenesis of neurological disorders.”

and, in the discussion of a professional textbook on the subject, that127:

“The role of free radicals and oxidative stress in neurological disorders has only recently been recognized… Oxidative Stress and Free Radical Damage in Neurology sets the record straight, focusing on clinical and research issues regarding the interplay of free radicals and the human nervous system. Crucially, the chapters cover numerous antioxidants and their possible therapeutic role in neurological disorders. Key illnesses such as epilepsy, multiple sclerosis and Parkinson’s are analyzed, and chapters also examine more general issues such as the link between free radicals and inflammation of the central nervous system..”

And again, to eliminate any doubts on relevance128:

“It has been demonstrated that oxidative stress has a ubiquitous role in neurodegenerative diseases.”

We see the consequences of oxidative stress over and over, and at this point we are not entitled to remain ignorant of what we can and must do to improve the situation.  The details and important role that anti-oxidants play in combating oxidative stress have been repeatedly emphasized in this report.  We must take advantage of that same information here as it relates to neurological functioning.

We have also introduced leading research on the importance of glutathione as it relates to neurological diseases and Parkinson’s disease.  It should be recognized that glutathione is one of the most powerful antioxidants known, and from the above, it should come as no surprise to us that its effectiveness against oxidative stress is important to neural functioning.  The importance of understanding the precursors of glutathione (e.g., N-acetyl cysteine (NAC) and alpha lipoic acid) vs. dietary supplemention or ingestion has also emphasized in this paper.

Through the introduction of iodine therapies that are practiced to improve the functioning of the thyroid, we have also learned that adequate levels of iodine are also strongly related to mental functioning, acuity and intelligence.  This topic is especially prominent in the presentation by Jorge Flechas, MD, above.  We have also learned that the difference between the federal guidelines of minimum daily iodine levels and the levels deemed beneficial by certain medical practitioners is dramatic, to say the least.  This dosage issue is entirely independent from any need to compensate for the potential reduction or removal of iodine stores within the body by competing aromatic halogen compounds (as they have been identified and postulated within this report).

We have also called strong attention to the intriguing and serious implications of oxydopamine and its related compounds within this growth form.    There is a strong case in the data of this report for this type of existence, and the damage that these compounds have upon neurological function is unambiguous.  Recall that such compounds are used in the laboratory to deliberately induce Parkinson’s Disease.  Such compounds reduce dopamine and brain amine levels and this, as a minimum, is known to affect memory loss and cognitive functioning.

With respect to the potential mitigation from this effect, oxidative stress is responsible for dopamine loss129, so this is now a familiar refrain to us.  The role of antioxidants has been discussed at length in this report, and this presents the roles and use of vitamins (e.g, A, B, C, D, E), enzymes,  and the precursors to glutathione for example.

Readers and health practitioners will also want to investigate the role of tyrosine and L-tyrosine as they relate to dopamine levels in the brain.  Tyrosine is an amino acid, and it is the building block for dopamine as it has been discussed.  The prospect of structural interference in the synthesis of dopamine has also been raised within this report, especially with prospect of halogen substitutions on the aromatic ring of tyrosine.

The role of diet and nutrition is also important to dopamine levels.130  I am hoping that it is now understood, from the journey that has been shared, that this researcher advocates nutrition as one of the primary pathways towards better health, and that those who are knowledgeable in such ways deserve our greater recognition and attention.  They have been driven to the heart of the matter, and that is that all life will eventually be a product of the nourishment that it consumes.  The business of “supplementation” is essentially a band-aid to attempt to compensate for a deficiency that never should have existed if we were wiser and more complete in our ways, especially from youth onwards.

While we are on the subject of nutrition, a specific nutritional drink recipe is available on this site.  This recipe is a culmination of health research by Carol Carnicom over a period of several years and it now also combines many of the important research findings from the study of the Morgellons condition.  It is a nutritional approach to some of the needs that have been established, therefore, from a variety of perspectives.   Protein sources, joint issues, iron utilization and the need for iodine are each examples of the ties that have evolved over the years between research and nutrition.  The reader may find this information to be of value in some unexpected ways, and I encourage you to become familiar with both its pleasures and its constitution.  The link to ”Carol’s Smoothie Recipe” follows below:

“Carol’s Smoothie Recipe”
(.pdf download)

Continuing on the subjects of neural, mental and cognitive functioning, some of the food sources that are known to benefit tyrosine and dopamine levels include, therefore131,

“Foods highest in L-tyrosine include:

  Fava beans



  Ricotta cheese


  Mustard greens


  Dark chocolate [Now, there’s an excuse…-CEC]


  Wheat germ ”

The role of diet, nutrition and enzmyes  in improved neural functioning is also discussed at length in the following report from the U.S. Department of Agriculture, entitled “Nutrition and Brain Function”.   We learn here again the important role that antioxidants play with the summary statement that:132  

“Perhaps there is no better place in which to gauge the power of antioxidants than between the minute connections of the nerve cells.”

Two additional points of interest are also mentioned in this report.  The first is the recognized benefits of enzymes (specifically, ‘kinase” enzymes) to brain functioning.    Notice also that even though the size of the brain is quite small relative to the body, it ends up using significant amounts of oxygen during mental activity.  The availability of sufficient oxygen and  body’s ability to use this oxygen effectively are obviously of importance here.   We see once again that it is a hopeless exercise to seek out singular causes, effects and ‘cures’ to the complex health problems before us, and the joint appearance of antioxidants and enzymes in the crusade against oxidative stress has again made its mark here.

Another word of importance within this paper concerns the regeneration of brain neuron cells, termed “neurogenesis”.  This work shows that adages die slowly, and that it is only recently accepted in the mainstream scientific community that the brain is not a fixed organ which can only deteriorate with age.  The research shows that brain neurons can be regenerated, albeit at a slower rate, at more advanced ages with proper nutrition.   This means “new” brain functioning and development can continue in the aging process and that “disease” is not a fixed sentence.   One must be careful of old adages, lest we become fixed ourselves in our ways, thinking methods and perceptions.

Additional well known natural approaches to improve mental clarity and function include those of Gingko Biloba and CoQ10.  Whether or not these particular supplements will be of known benefit with the Morgellons situation remains to be seen; they have, however, established reputations with respect to improving mental clarity and memory loss.  The following paper133 discusses a series of natural remedies to enhance memory and mental function, and it is anticipated that they may be of some benefit.

Enhancing Memory and Mental Functioning – NYU Langone Medical Center



It is a primary argument of this researcher that the solution to a problem is not necessarily found by introducing additional complexity into the situation.  The case for “supplementation” of diet to compensate for health problems is a primary example of this dilemma.  If one has known sources for health problems, it is usually wiser to eliminate the source of the problem rather than try to compensate for it with an infinite combination of variables, such as pills, supplements, or drugs, for that matter.  The proper approach for the “Morgellons” condition, as with any health impairment or “disease” is to strike to the source of the matter.  If the cause or source of such a condition can be identified, it is to be removed or stopped in its tracks, if at all possible.  It is not be be accepted as intrinsic to the environment and then compensated for with a  myriad of protocols, drugs, treatments, and supplements  in a state of perpetual uncertainty and ignorance.  A body of information is available to those who wish to seek it out, and this information (along with your participation) can be a pathway towards striking at that source of health and disease.  The general population, the health communities, the professional communites, and the governmental structures are obligated, as has been stated repeatedly, to combine, use and express their knowledge and talents to improve the state of the environment and the health of the people.  We, our children, and our future children deserve no less than this, and the entire world deserves the more of it.

This episode of research now comes to a close; this paper has taken more than a year to complete and additional needs remain before us.  Additional work will be done in the future to summarize and consolidate the essentials of this research.    Work of this nature is a journey in itself, and I do not know where it will lead and end when I start.  The process of identification, correlation and analysis has now taken place, and it is hopeful that it provides a beneficial foundation from which we may accomplish greater things in the future.  I thank you for your patience and endurance to reach these closing comments and I hope that the work has been of value to the general readership.  The future remains to be influenced by the decisions and actions that we now take together.




Clifford E Carnicom
(born Clifford Bruce Stewart, Jan 19 1953)

Additional Note:

Appreciation is extended to Lucretia Smith and Dr. Jimmie McClure for their sustained interest, research and communication to CI over a period of several years about the importance and relevance of thyroid issues to the work presented here.  These individuals, along with others, deserve credit for their prescient assessments of the role that thyroid dysfunction is likely to play in the “Morgellons” condition. Many thanks to both of you.


Clifford E Carnicom



1. Infrared Absorption Spectroscopy – Practical, Koji Nakanishi, Holden-Day, Inc., 1962.

2. Reprint of Colthrup Chart of Characteristic Group Absorptions in Modern Methods of Chemical Analysis, Robert L. Pecsok, John Wiley & Sons, 1976.

3. IR Pal Software 2.0, Dr. Wolf van Heeswjik, 2010, Wolf’s Shareware and Freeware,

4. Spectral Database for Organic Compounds (SDBS), National Association of Advanced Industrial Science and Technology (AIST), Japan.

5. Biochemistry, John T. Moore, Wiley Publishing, 2008.

6. Organic Chemistry, John McMurry, Brooks/Cole, 2004.

7. Ibid., McMurray.

8. Oxford Dictionary of Science, Oxford University Press, 1999.

9. Organic Chemistry, Bruce A. Hathaway, Ph.D., Barron’s, 2006.

10. Biochemistry, John T. Moore, Wiley Publishing, 2008.

11. Chemistry, The Central Science, Theodore L. Brown, Pearson Prentice-Hall, 2006.

12. Ibid., Moore.

13. Ibid., Hathaway.

14. Ibid., Oxford.

15. Ibid., Brown.

16. Ibid., McMurray.

17. Ibid., Oxford.

18. Ibid., McMurray.

19. Principles of Biochemistry, H. Robert Horton, Prentice Hall, 1993.

20. Ibid., Oxford.

21. Ibid., McMurray.

22. Ibid., Hathaway.

23. Ibid., Oxford.

24, 25. Ibid., McMurray.

26. Ibid., Oxford

27. Ibid., McMurry

28. Ibid., Oxford.

29. Morgellons : A Thesis, Clifford E Carnicom, Oct 2011,

30. Morgellons Research Project : Scientific Study of the Morgellons Condition, Carnicom Institute.

31. Free Radicals in Biology and Medicine, Dr. P.K. Joseph

32. Iron Deficiency, Wikipedia,

33. Amino Acids Verified, Clifford E Carnicom, Nov 2012,

34. Amino Acid Chart, Dr. Guy Wilson,

35. Ibid., McMurray.

36. Principles of Biochemistry, Albert L. Lehninger, Worth Publishers, 1982.

37. ATSDR – Medical Management Guidelines : aniline, U.S. Department of Health and Human Services, CDC.


39. Effects of Acidity, Dr. Michael Lam

40. pH Balance and Your Health,

40b. The Acid Alkaline Food Guide, Dr. Susan E. Brown, Square One Publishers, 2006.

41. Are Your Teeth at Risk,

42. Robbins Pathological Basis of Disease, Ramzi S. Cotran, M.D., W.B. Saunders Company, 4th Edition, 1989.

43. Biochemistry Demystified, Sharon Walker, Ph.D., McGraw Hill, 2008.

44. Ibid., McMurray

45. Ibid., Morgellons : A Thesis, Carnicom

46. Aromatic Substitution Reactions Part II,

47. General Discussion of Common Mechanisms for Aromatic Amines, IARC.4

48. Oxidopamine,

49. Hazardous Materials Chemistry for Emergency Responders, Second Edition, Robert Burke, CRC Press, 2003.

50. Hepatotoxicity and mechanism of action of haloalkanes: carbon tetrachloride as a toxicological model., BioInfoBank Library, Critical Reviews in Toxicology, Nov 29, 2012.

51. Mechanism of Anesthetic Toxicity: Metabolism, Reactive Oxygen Species, Oxidative Stress, and Electron Transfer, ISRN Anesthesiology Volume 2011.

52. Organometallic Compounds, Michigan State University, Department of Chemistry,

53. Halogens & Their Compounds: Health Hazards, International Labor Union,

54. Spectral Database for Organic Compounds (SDBS), National Institute of Advanced Industrial Science and Technology (AIST), Japan

55. Effect of 6-hydroxydopamine on brain norepinephrine and dopamine: Evidence for selective degeneration of catecholamine neurons, George R. Breese, National Institutes of Health.

56. Desipramine attenuates working memory impairments induced by partial loss of catecholamines in the rat medial prefrontal cortex, SM Clinton, National Institutes of Health.

57. Ibid., Cotran.

58. Ibid., Cotran.

59. Morgellons : In the Laboratory, Clifford E Carnicom, May 2011,

60. Morgellons, The Breaking of Bonds and the Reduction of Iron, Clifford E Carnicom, Nov 2012,

61. Ibid., Morgellons : A Thesis, Carnicom

62. Risks of Iron Supplements,

63. Ibid., Risk of Iron Supplements

64.The role of vitamin C in iron absorption, L. Hallberg, National Institutes of Health.

65. Ibid, Morgellons, The Breaking of Bonds and the Reduction of Iron, Carnicom.

66. Ibid., Morgellons : A Thesis, Carnicom

67. Ibid., Amino Acids Verified, Carnicom.

68. N-acetylcysteine (NAC), David Wheldon.

69. A Mechanism of Blood Damage, Clifford E Carnicom, Dec. 2009,

70. Ibid., Morgellons : A Thesis, Carnicom

71. Ibid., Morgellons : A Thesis, Carnicom

72. Ibid., A Discovery and A Proposal, Clifford E Carnicom, Feb. 2010,

73. Ibid., Cotran.

74. Ibid., A Discovery and A Proposal, Carnicom.

75. Free radicals, antioxidants, and human disease curiosity, cause, or consequence?, Barry Halliwell, Lancet, Sept 10, 1994 v344 n8924 p721(4), published at

76. Ibid., Cotran.

77. Oxidative Stress and Neurodegenerative Diseases: A Review of Upstream and Downstream Antioxidant Therapeutic Options, Current Neuropharmacology, Mar. 2009, Bayani Utara, National Institutes of Health.

78. Free Radicals, Oxidative Stress, and Diseases, Enrique Cadenas, MD PhD, Professor of Pharmacology, University of Southern California.

79. Alcohol, Oxidative Stress and Free Radical Damage, Defeng Wu, PhD, Alcohol Research & Health, National Institues of Health.

80. Ibid., A Discovery and A Proposal, Carnicom

81. Ibid., Cotran.

82. Ibid., Cadenas.

83.Ibid., Cadenas.

84. Structure and reactivity of radical species, University of California at Davis.,

85. Diradical Chemistry, The Chemogenesis.,

86. Magnetic Liquid Oxygen, University of Illionois, Chemistry Department.

87.The Balancing of Oxidants and Antioxidants, Pharmaceutical Field,

88. Ibid., Cadenas.

89. Ibid., Pharmaceutical Field.

90. Ibid., Pharmaceutical Field.

91. Ibid., Pharmaceutical Field.

92. Free Radicals and Reactive Oxygen, Colorado State University, Biomedical Hypertexts.

93. Ibid., Colorado State University.

94. Ibid., Morgellons, The Breaking of Bonds and the Reduction of Iron, Carnicom.

95. Morgellon’s : The Role of Atmospheric Aerosolized Biological Nano-Particulates, An Anonymous Physician.

96. Ibid., Morgellons, The Breaking of Bonds and the Reduction of Iron, Carnicom.

96b. Oxidata Test,

96c. Free Radical Urine Test,

96d. How Do Anioxidants Work Anyway?, Kristy Russ,

97. Wikipedia.

98. Ibid., Wikipedia

99. Understanding Urine Tests, National Institutes of Health,

100. Acidic Body, Michael Lam MD,

101. Acid Base Balance in Critical Care Medicine, Patrick J Neligan, Clifford S Deutschman, Patrick Neligan Deparment of Anesthesia, Univ. of Pennsylvania, 2005.

102. Acid-Base Tutorial, Dr. Alan Ggrogono, Tulane University Department of Anesthesiology,

103. Ibid., A Discovery and A Proposal, Carnicom, Feb. 2010.

104. Morgellons : Growth Inhibition Confirmed, Clifford E Carnicom, Mar 2010,

105. Ibid., Morgellons : A Thesis, Carnicom

106. Alkaline Water and Why Avoid It, Lawrence Wilson, MD, Center for Development, Inc.,

107. Sugars and dental caries, Riva Touger, The American Journal of Clinical Nutrition.

108. Urine and Saliva pH Testing, Michael Biamonte, C.C.N,

109. In Office Lab Testing : Functional Terrain Analysis, Dr. Dicken Weatherby,

110. Dr. Henry G. Bieler, Wikipedia.

110b. Complete Practitioner’s Guide to Take-Home Testing : Tools for Gathering More Valuable Patient Data, Dr. Dicken Weatherby,

111. Lactic Acidosis, Wikipedia.

112.Relation Between Low Body Temperature and Thyroid,

113. Metabolic Temperature Graph, Bruce Rind M.D.,

114. Ibid, Weatherby.

115. Iodine and Detoxification, Dr. Mark Sircus.,

116. Thyroid Balance, Dr. Glenn Rothfeld, MD, Amaranth, 2003.

117. How Adrenals Can Wreak Havoc,

118. Ibid., Weatherby.

119. Unconventional Tests and Procedures to Diagnose Thyroid Diseases,

120. Tincture of Iodine, Wikipedia

121. Povidone Iodine, Wikipedia

122. Toxicity Profile, Polyvinylpyrrolidone,

123. Medline Plus : Iodine, National Institutes of Health

124. The Great Iodine Debate,

125. Ibid., Cotran.

126. Oxidative stress and neurological disorders in relation to blood lead levels in children, M Ahamed, National Institutes of Health.

127. Naton Gadoth, Oxidative Stress and Free Radical Damage in Neurology, Springer, 2011.

128. Oxidative Stress in Neurodegeneration, Varsha Shukla, Hindawi Publishing Corporation, 2011.

129. Katlid Rahman, Studies on free radicals, antioxidants, and co-factors, National Institutes of Health.

130. Bryce Wylde, The Dopamine Diet,

131. Ibid., Wylde.

132.James A. Joseph, Nutrition and Brain Function, U.S. Department of Agriculture.

133. Enhancing Memory and Mental Functioning , NYU Langone Medical Center,

Environmental Filament : Keratin Encasement

Environmental Filament : Keratin Encasement
Clifford E Carnicom
Jan 07 2013


It can now be established with a high degree of certainty that the external casing of the environmental filament samples are composed of keratin or a keratin-like material.  This supposition has been in place for a number of years by this researcher; it can now be demonstrated to be the case by direct chemical and spectroscopic means.  Certain ramifications of this finding, in conjunction with earlier work, are as follows:

1.  It is deduced that the environmental filament is not a naturally occurring material. 

2. The filaments contains non-keratin based chemical and biological components within the internals of the filaments.   Considerable information regarding the nature of the environmental filaments is available on this site; this information has been accrued over a period of several years of progressive research.

3. The emphasis upon study of the filaments is to be directed to the sub-micron components (biological and chemical) that are internal to the filaments.  The keratin aspect of structure is to be interpreted as an encasing mechanism only.

4.  The filaments are not hair or spider webs. 

5.  A false laboratory report has been issued in the past regarding the identification of this filament material (to be discussed in a separate report). 

The primary method by which this conclusion has been reached is with chemical and spectroscopic comparison of a known source of keratin with the environmental filament by similiar means.  This comparison has been made possible with the recent advance in methods of chemical decomposition of keratin based substances by this researcher.  Please see the report entitled “Environmental Filament Penetrated” for this discussion and presentation. 

human hair serbian sample
Human Hair Environmental Filament Sample

Spectroscopic comparisons of keratin obtained from human hair and the same substance obtained from the environmental filament casing are shown immediately below; it will be seen that they are essentially identical.  Additional notes and discussion will follow below the spectra.

spectroscopic analysis of keratin

A visual light spectroscopic analysis of keratin obtained from the decomposition of human hair in combination with ninhydrin and heating.  Human hair is composed predominantly of keratin.


spectroscopic analysis of the environmental filament


A visual light spectroscopic analysis of the environmental filament after chemical decomposition and in combination with ninhydrin and heat.  It will be seen that the spectrum obtained is essentially identical to the keratin spectrum above. The keratin of the environmental filament is interpreted as an encasement structure and it does not account for the biological components that have been repeatedly identified within this protein housing.


colored solutions


A photograph of the colored solutions subjected to visual light spectroscopic analysis.  The solutions result from chemical decomposition of keratin based structures, in combination with heat and ninyhdrin.  The solution on the left is derived from the environmental filament sample; the solution on the right is derived from human hair.  Both hues and spectra can vary to some degree by concentration levels within a solution; these examples and spectra indicate a coincidence of relative concentration in each case.



Additional Notes:


Keratin is an especially impervious protein structure.  Observation and study of your own hair is a very good analogy for understanding the hardiness of this particular protein.  During the recent trials of study in decomposition, chemical penetration of hair itself represents an excellent example of the challenge of examination of the environmental filaments and their internals.  Numerous trials were conducted using strong solutions of sulfuric acid, sodium hydroxide, nitric acid, salicylic acid, sodium hypochlorite (bleach), ammonium thioglycolate and others.  All essentially met with failure to the degree needed with the time available.  Although some mild success was achieved with a hair sample, the environmental filament sample remained essentially impervious to almost all methods.  The best success of decomposition has eventually come forth with the use of a commercial hair declogger used in plumbing systems.  This solution is primarily a combination of concentrated sodium hydroxide and concentrated potassium hydroxide.  This solutions is highly caustic. The greater success of this method also becomes  dependent upon the use of applied heat over an extended time period. It was with the use of this method that valid comparisons, both chemically and spectroscopically, could be made.  Considerable work remains before us to acquire the detailed biochemical knowledge of the internal nature of the environmental filaments; this work will continue as the proper resources and equipment avail themselves.


Morgellons : The Breaking of Bonds and the Reduction of Iron

Morgellons :
The Breaking of Bonds and the Reduction of Iron

Clifford E Carnicom
Nov 03 2012

Note: I am not offering any medical advice or diagnosis with the presentation of this information. I am acting solely as an independent researcher providing the results of extended observation and analysis of unusual biological conditions that are evident.  Each individual must work with their own health professional to establish any appropriate course of action and any health related comments in this paper are solely for informational purposes and they are from my own perspective.


Three methods that appear to interfere with the molecular bonding of the iron-dipeptide complex that is now understood to be characteristic of the “Morgellons” growth structure have been established and identified.  The iron-protein complex is believed to be of, or similar to, the “Rieske Protein” (iron-sulfur) form.  These three methods also appear to be variably successful in reducing the oxidation state of the encapsulated iron from the Fe(III) state to the Fe(II) state.  The discovered methods involve the use of ascorbic acid (Vitamin C), N-acetyl cysteine (NAC) and glutathione.  The results of applying glutathione appear to be especially promising at this time, as it appears that a major disruption in the bond structure has taken place after approximately 72 hours.  The methods have been established and verified through visual, chemical and spectroscopic methods and each has an effect independent of the others.  The hypothesis to be made here is that the growth of the organism itself may be interfered with as a result of this work.

This result has been a primary target of research through this past year, and it may represent an important potential inhibitor to the structure growth.  The results may also indicate a certain level of coincidence of research or result that has been achieved; an interest in the use of NAC as a mitigating influence (i.e., bio-film reduction) by direct experience has been expressed by independent parties over time1.  Synergetic use of all three compounds is also a prospect for investigation.  Additional research will seek out the particular chemistry of the disassociation and reduction process (see Additional Note below).  Intensive and exhaustive study of the molecular structure of the proteinaceous compound with more sophisticated equipment remains in need.

It will be found that there are important interactions and relationships in the body between cysteine compounds, NAC and glutathione.  The combination of influences and interactions between iron, cysteine, histidine, ascorbic acid, N-acetyl cysteine and glutathione represents an important pathway of research for the Morgellons condition.  These considerations are to be added to those that have also been outlined in previous research papers on this site in recent years.  Full consideration of all information that has been made available may be beneficial in developing any strategies of mitigation for the condition.

All tests have been conducted within a laboratory setting and they do not involve the human body in any fashion; please note the caution at the introduction of this paper.  Formidable difficulties remain with the consideration of the highly impervious casing (likely keratin based) that encapsulates the internal growth forms and the environmental forms.  The work herein, in combination with the importance of iron within the structure, as well as specific amino acids (cysteine and histidine) that have been identified as a part of the growth form, may represent important milestones in the prolonged research of the so-called “Morgellons” condition.

Listen to a Research Discussion on This Topic

Additional Discussion:

The iron in an oxidized Rieske protein form exists in the Fe(III) state.  In the reduced Rieske protein form, one iron atom is in the Fe(III) state and the other iron atom is in the Fe(II) state.  The iron-sulfur centers perform a function of electron transfer by alternating between the oxidized and reduced state; this is known as a redox couple.   Ascorbic acid and NAC are both known to be powerful reducing agents.  Glutathione is also a powerful reducing agent and it is a tripeptide that is known specifically to be able to break disulfide bonds.  Disulfide bonds have long been though by this researcher to be a key element of the structural framework of growth.  It can be shown directly by chemical tests that ascorbic acid, NAC and glutathione reduce iron from the Fe(III) state to the Fe(II) state.  It is anticipated that this fact plays an important role in the protein (dipeptide) bond disruption that has been identified in this report

The inability of glutathione to be effectively absorbed in the human digestive system is another important consideration; attention must be given to the “precursors” of formation of glutathione, such as N-Acetyl Cysteine ( NAC), denatured whey and cysteine-rich foods.  Please refer to the research discussion and the informational videos linked into this report for additional information on this important aspect of this research.

(Note the references to N-Acetyl Cysteine (NAC) and whey(lactoferrin) in the second video of the series(Dr. Mark Hyman))
(No endorsements of products to be implied or stated herein)

Dr. David Perlmutter
Glutathion Therapy – Part I (2 min)

Dr. David Perlmutter
Glutathion Therapy – Part II (5 min)

 ferric (III) chloride

A Demonstration of the Reduction of the Ferric (III) Iron Ion to the Ferric (II) Iron Ion Using Glutathione. 
Both test tubes contain a solution of ferric (III) chloride.  In addition, glutathione has been added to the test tube on the right.  Both test tubes are subsequently tested for the presence of the ferrous(ii) ion.  The test tube on the right with glutathione passes this test; the test tube on the left fails the test.  This demonstrates the ability of glutathione to reduce iron from the ferric (III) to the ferrous (II) state.  The spectrophotometer graphs that follow within this report demonstrate this same phenomenon using developed cultures from oral filaments, i.e, a reduction in the iron oxidation state indicated by a shift  of the wavelengths toward the red portion of the spectrum with the addition of glutathione and other anti-oxidants to the culture extracts. 

Chemistry for the Life Sciences, Rutton, 2003.

Source : Chemistry for the Life Sciences, Rutton, 2003.

The diagram above shows how gluathione is effective in breaking down disulfide bonds that are an integral part of the growth structure of the cultured forms.  Sulfur is indicated by ‘S” in the sketch and the sulfhydryl group (sulfer attached to hydrogen) is indicated by “SH”.  The disulfide bond is indicated by the two S units linked together in the left segment of the diagram.  The irregular structure is essentially arbitrary in form and could represent a proteinaceous structure, for example (as in this report).

The objective of the graphs below is to demonstrate, in much greater detail, a particular shift in color that takes place with the addition of certain antioxidants (vitamin C, NAC and glutathione).  The shift in color occurs (towards the red end of the spectrum, peaking at approximately 490 nanometers (nm)) with the addition of a specific chemical reagent that turns red in the presence of ionic iron (Fe+2 and Fe+3).  This test is useful from two standpoints: It detects both the breakdown of the iron-sulfur  bonds within the core of the dipeptide and it demonstrates the reduction of the coordinated iron complex to ionic form(Fe+2).

Visible Light Spectrum of Oral Filament Culture Fe(III) Test (negative result)

Visible Light Spectrum of Oral Filament Culture Fe(III) Test (negative result)

The graph above serves as a reference spectrum for us.  The sample for the spectrum is an extract from the numerous identical cultures that have been developed from oral filament samples.

The extract is formed in the following fashion:  The culture is fully developed into the filamentous form.  The culture is then removed from the growth medium (in this case red wine), thoroughly rinsed and then dried by subjecting it to low heat for a prolong period.  The dried culture is then pulverized to a powder state with mortar and pestle.  After drying and pulverization, the sample subjected to a sodium hydroxide (lye) solution along with heating to the boiling  point.  This process will break down the growth form sufficiently to at least partially dissolve the powdered form to produce a colored solution, which is required for visible light spectral analysis.  The heat and lye process is a known method that will break down, at least in part in this case, proteinaceous materials.   The color of solution that results is dark brown.  This alkaline solution is then filtered into a storage container and exists as a concentrated extract of the original culture.

All information at this time indicates that it can be stored essentially indefinitely in this state without biological degradation; subsequent cultures can be developed further at any time in ease.  This result strongly suggests that a “spore-like” state of existence is in place under these circumstances. This fact has actually been demonstrated earlier on many occasions, such as the development of cultures from environmental filaments (e.g, the “EPA” filament)  ten years after the original collection.  As has been repeatedly expressed, there appears to be no significant chemical , biological or morphological difference between the environmental filament samples the oral filament samples, the skin lesion filament samples and the culture filament samples.  This statement alone is profound with respect to expected distribution of the “Morgellons” condition.

The extract that has been created is too concentrated to use directly in spectral analysis; it must be diluted to allow sufficient light to pass through the solution.  In the case above, approximately four drops of the extract are placed into approximately three milliliters (ml) of distilled water; the original solution and culture spectrum under the lye-heated treated condition is a pale brown.  It is of passing interest that this color alone corresponds well with that of the hydrated ferric ion complex.  The subject of iron within the growth form has been discussed at great length in prior reports (e.g., see Morgellons : A Thesis).

For the purpose of this study, the sample is then subjected to a chemical reagent (potassium thiocyanate) that is extremely sensitive to the presence of the ferric iron state, i.e., ionic iron iron in the +3 oxidation state (III).  This reagent will cause a solution to turn red in the presence of the ferric ion.  Spectral analysis is useful here as it can graphically demonstrate shifts in frequency that may not be apparent to the human eye.  In the case above, there is no discernible difference in color by eye or by spectral analysis with the addition of the Fe(III) detection reagent.  This proves to us that iron in the ionic state of +3 does not exist in the original culture extract.  It says nothing about the presence of iron forms that may exist in other states (e.g. such as a coordinated iron complex) as we shall soon see.  These complexities of the iron presence issue have also been discussed at length in the previously mentioned report.

The spectrum is then taken after the Fe(III) reagent detection addition and the result is shown above as a reference spectrum.  What we observe in the visible light portion of the spectrum is  a fairly monotonic and steady decrease in absorbance as the wavelength decreases.  It would be of great value to extend this spectral analysis into the infrared and ultraviolet regions, but this equipment is considerably more expensive to obtain and it is not yet available to the Institute.  The resources to expand the current analysis remain in great need.  This spectrum, nevertheless, is of great value as a reference point, and it suffices to be able to detect the shifts in frequency that result from the anti-oxidant studies that are the basis of this report.

Visible Light Spectrum of Oral Filament Culture Fe(II) Test (negative result)

Visible Light Spectrum of Oral Filament Culture Fe(II) Test (negative result)

The description for the graph above is identical to that of the previous one with one important exception.  In this case the reagent that has been applied (1,10 phenanthroline) is a test for the presence of the ferrous (Fe+2) iron state(II) within the culture extract vs. the ferric (III) form.  This test result is also negative and it likewise shows that iron (III) does not exist in ionic form within the culture extract.  Equally, it says nothing about the existence of iron in another form (e.g. ionic or complexed state) within the culture extract.  The importance of the state of iron that exists within any compound or complex is therefore paramount and it will be demonstrated further later in this report.

Visible Light Spectrum of Oral Filament Culture Fe(II) Test NAC (positive result)
Note shift toward the red portion of the spectrum.

This spectrum shows an important difference with the two reference graphs that have been previously presented.  This particular sample has N-acetyl cysteine (NAC) applied to the culture extract in addition to the reagent for the detection of iron (III).  What is important to observe here is s the shift in frequency toward the red portion of the spectrum.  What this means, in simpler terms, is that iron in the ferrous ionic state (III) has now been detected.

This change means that two very important changes have taken place.  First, the bonds that hold the iron within the growth structure have been broken to release the iron in the first place.  Secondly the iron is the the reduced state of Fe(+2), or in the state that is again able to combine with oxygen in hemoglobin. These two findings potentially represent distinct advantages in the quest to “interfere” with the growth stages of this (i.e., “Morgellons” associated) organism.  Thirdly, this particular anti-oxidant (reductant) can be incorporated into general health improvement regimens as it is already widely known and used to that end in the health and medical communities.

Visible Light Spectrum of Oral Filament Culture Fe(II) Test Ascorbic Acid  (positive result)
Note shift toward the red portion of the spectrum.

The discussion as it relates to NAC above can be applied equally in this case, but again with one important exception.  In this case, the added agent to the culture extract is ascorbic acid, or Vitamin C.  All conclusions above made with respect to the use of NAC above remain similar and valid with the use of ascorbic acid.  The reduction level  in both cases appears to be relatively weak, i.e. the shift in color is also detectible by eye, but barely so.  The ability to break the iron-disulfide bond complex (as concluded by the detection of iron oxide and cysteine within the complex) and to reduce the iron to a free +2 state is of potentially monumental significance.

It is also wise to recall earlier research that indicated a level of effectiveness in inhibiting the growth of the culture using ascorbic acid as well.  That earlier research may be deserving of additional attention and repetition in light of these current findings.  It may well be found that there will be associated relationships, particularly in the anti-oxidant (i.e., reductive) qualities of ascorbic acid.  Recollection of the mechanisms involved in the “Fenton” reaction may also serve us well in the near future and they too have been described within earlier research.

Visible Light Spectrum of Oral Filament Culture Fe(II) Test Glutathione (positive result)
Note shift toward the red portion of the spectrum.

The case of using glutathione as an anti-oxidant (or as a reducing agent) is an especially interesting one.  The call to consider the use of glutathione was based upon research related to the need to break down disulfide bonds, and as such it arose from a strongly directed proposition.  The results have been favorably surprising and they have led to an in-depth interest in glutathione and to how it affects our health in the main.

With respect to the spectrum immediately above, we can actually regard it as being essentially equivalent to the two previous cases, i.e., NAC and ascorbic acid.  There is indeed  a shift in the wavelength towards the red end of the spectrum (indicating the presence of Fe(II), but it continues to affect the culture in a relatively weak sense.  Our pleasant surprise comes with the final spectrum shown below.

Visible Light Spectrum of Oral Filament Culture Fe(II) Test Glutathione after 72 hours. (positive result)
Note major shift toward the red portion of the spectrum.

This last case, again involving the use of gluthathione as a reducing agent, has come about by “accident”.  Many acts of discovery seem to follow that fortuitous path.  What has happened here is that the test tube was allowed to sit for approximately three days.  At the end of this period the extract solution had turned a bright and visible red.  The spectrum above is another way of verifying this same fact; peak absorbance has been clearly, strongly and definitively shifted toward the reddish portion of the spectrum, peaking at approximately 500 nm.  The reddish color appears, again, because of the induced presence of the ferrous iron ion by the glutathione, in addition to the breaking of the bonds that encapsulate (or chelate) this same iron.

What this means, also in simpler terms, is that glutathione (with the sufficient passage of time) is quite effective in breaking down the bonds in the proteinaceous complex that has been identified within the “Morgellons” growth form.  In addition, it appears equally and concomitantly effective in releasing and reducing the free iron to a +2 oxidation state.  Iron is required to be in the +2 oxidation state to bind to oxygen within hemoglobin.

The aggregate impact of these anti-oxidants (reducing agents) does hold some promise for us.  Interference with the bond structure of the dipeptide that has been identified, along with the release of the chelated iron within the complex, have been the primary goals of this researcher for some time now.  The continued pursuit of this strategy appears to remain as a wise choice of energy, effort and research.  The pace and depth of this research can be increased with proper support, should it ever come to pass.  There remain other viable strategies as well to be explored.

Readers , as always, are advised to consult with their health practitioners as to how this information may be best put to use.  For instance, the complexities of glutathione actions within the body do not allow for simple “replacement by supplement”.  There is a host of knowledge about the “precursors” of glutathione that is required to more effectively use the information and discoveries within this report.  Nevertheless, the role of anti-oxidants (reducing agents) with particular emphasis upon glutathione, N-acety cysteine and ascorbic acid appears to be justified with promise at this stage.  Readers may wish to avail themselves of additional mitigating strategies that have been enumerated within the numerous research papers on the Morgellons issue within this site.


Clifford E Carnicom
October 27, 20122,3,4


Additional notes:

1  Appreciation is extended to Sandra Autry, former Carnicom Institute Associate Member, for her interests, recommendations and experiences expressed on this topic – Personal conversation.

2.  Many thanks to Carol Carnicom for her recent expressive cello playing in Devorak’s New World Symphony, which served as a dramatic and energetic backdrop to one of the sessions for this report.

3. This paper authored by Clifford E Carnicom, originally entering  this world as Clifford Bruce Stewart, born January 19, 1953.  Call it a journey of adoption.

4.Many thanks to the Pecos River at Villa Nueva in New Mexico, where the vestiges of Indian summer have graciously closed down this report..