Followers

Google+ Followers

Thursday, October 8, 2009

Oct.9 - MORGELLONS : A STATUS REPORT‏

Dear Friends,
Click the link if you don't receive the images.

MORGELLONS : A STATUS REPORT
Clifford E Carnicom
Oct 08 2009

This page is subject to additional edits.

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.

SUMMARY STATEMENT:

A partial summary of the research accumulated through this site on the so-called "Morgellons" issue is as follows:

1. The internal filament repeatedly described, as in the dental extraction samples, appears to be a primary pathogenic form. These internal biological filaments have been identified, to a varying degree, in essentially all individuals that have participated in the testing process thus far. The blood of participating individuals also displays, to a high correspondence, anomalies in structural integrity. A sub-micron spherical structure, to be assessed in further detail at a later point, also commonly occurs within the erythrocytes.

2. The morphology, size, structure and chemistry of these internal filaments appears to be highly similar to that of certain environmental filament samples, notably that which has been refused by the Environmental Protection Agency (EPA) for identification. In addition, numerous research papers over the last ten years document the repeated detection of unusual biological components within a series of environmental samples, including that of erythrocytic (red blood cell) forms.

3. Numerous cultures have been developed from the internal filaments on agar and in wine based mediums. These cultures are essentially identical in form and chemistry with that of the original internal biological filament samples.

4. The cultures produced from the internal biological filaments (dental samples) have been shown to produce an erythocytic form. These cultures have produced a positive result for the existence of hemoglobin by two separate forensic level tests. The determination of the erythrocytic form is also repeatedly evidenced by direct observation, measurement and biconcave morphology.

5. The production of erythrocytic forms within direct biological filament samples and by culture is completely outside the known boundaries of conventional science and biology. It is repeatedly evident that these same erythrocytic forms can withstand (and even flourish in) extremely adverse environmental, chemical and thermal conditions. The evidence thus far indicates the original erythrocytic form is dessicated or spore-like and a reconstitution process is required to bring the cellular structures to full form and activity.

6. A method has been developed to break down the outer casing of the internal biological dental filaments. The internal components of these filamaments have been examined in detail upon repeated occasions. Two main structures emerge: an erythrocytic form and a sub-micron spherical form. The best current assessment of the sub-micron spherical form is that of being Chlamydia-like, with a special interest in Chlamydia Pneuomonia. Mycoplasma forms are also strong candidates of consideration as a "tertiary form" that is also frequently observed. Please also refer to the the paper entitled Pathogens and the General Population, April 2008, for the introduction of the Chlamydia-like structure as a primary topic of interest; the rationale of identification for this candidate remains. In addition, recent size measurements and the response of the Chlamydia-like structure to Giemsa stain further solidifies that rationale.

7. There is a strong consideration that the internal structures from the internal biological filaments are of a synthetic or artificial nature. This assessment is based upon an observed unifomity in geometry as well as the hostile chemical environment under which reconstitution takes place.

8. The internal biological filaments and the cultured form of the filaments have been subjected to the same chemical and thermal breakdown process. The same two internal sturctures are evident and observed in each case, that of an erthyocytic form and a Chlamydia-like form.

9. The existence of the internal biological filaments, the existence of introduced or modified erthrocytic forms, the Chlamydia-like strructure and the tertiary form are interpreted by this researcher to be critical and central aspects of the " Morgellons" condition. It is accepted that numerous symptom manifestations are reported in association with the condition; this report simply enumerates that which exists as a common denominator within all studies conducted thus far.

10. The source of the erythrocytic form and the Chlamydia-like organism is the filament under study, either in the direct biological internal form or identically from the cultured source. This assessment is reached through direct observation.

11. Success has been achieved in developing a solution based culture that originates from the decomposition (chemical and thermal) of the cultured filaments. A complete cycle of growth has been obtained. An aqueous or solution based culture development has numerous advantages in the development and application of experimental procedures. This culture work is based upon the following sequence:


1. Original filament form (biological or cultured).
2. Decomposition of the filament through chemical and thermal processes.
3. A single drop of the resulting solution is sufficient to reproduce the entire cycle.
4. The decomposed filament solution is cultured in a wine medium.
5. Two structures appear simultaneously over a period of several days within the solution when observed under the micrsocope: The Chlamydia-like form and the pleomorophic form (Mycloplasma candidate). Visually this material has an appearance similar to that of the original dental filament extractions, but not as fully developed.
6. Lastly, the original filament form (white in color) appears on the surface of the solution, completing the full cycle of development and growth.

12. The recent solution-based culture work infers that four varying components comprise the basic pathogenic form:


1. The encasing filament which appears to serve the purpose of housing, transport and delivery of the internal components.
2. An ethryrocytic form (primarily internal to the filament)
3. A Chlamydia-like structure ( primarily internal to the filament).
4. An apparent pleomorphic form (primarily internal to the filament). One candidate of identification is a Mycoplasma variant.
5. All items listed require positive analytic, chemical and biological testing and identification; candidate mention is dependent upon resources available at this time. The ability of the structures to withstand hostile and adverse chemical and environmental conditions strongly indicates modification to originating organisms or structures.

13. It can be shown by direct observation that the cultured filaments, after decomposition through chemical and thermal processes, appear to be the source of the blood anomalies first reported on by this researcher in November and December 2007. It is anticipated that the direct biological form of the filaments is likely to produce an identical result, as the cultured forms derive from the direct biological forms. Please also refer to the papers entitled Blood Testing and Morgellons : Airborne, Skin and Blood - A Match for a partial background preparation on this subject. Three structures are observed in the process : erythrocytic, Chamydia-like, and a "pleomorphic" (many form) ribbon or sausage-like form as shown in these original papers. A mycoplasma form is a viable candiate for the "pleomorphic" (tertiary) form.

14. Some of the primary functions of the blood include:

1.

Transports:

Dissolved gases (e.g. oxygen, carbon dioxide);

Waste products of metabolism (e.g. water, urea);

Hormones;

Enzymes;

Nutrients (such as glucose, amino acids, micro-nutrients (vitamins & minerals), fatty acids, glycerol);

Plasma proteins (associated with defence, such as blood-clotting and anti-bodies);

Blood cells (incl. white blood cells 'leucocytes', and red blood cells 'erythrocytes').

2.

Maintains Body Temperature

3.

Controls pH

The pH of blood must remain in the range 6.8 to 7.4, otherwise it begins to damage cells.

4.

Removes toxins from the body

The kidneys filter all of the blood in the body (approx. 8 pints), 36 times every 24 hours. Toxins removed from the blood by the kidneys leave the body in the urine.
(Toxins also leave the body in the form of sweat.)

5.

Regulation of Body Fluid Electrolytes

Excess salt is removed from the body in urine, which may contain around 10g salt per day
(such as in the cases of people on western diets containing more salt than the body requires).

Source: Structures and Functions of the Blood
Ivy Holistic
http://www.ivy-rose.co.uk/HumanBody/Blood/Blood_StructureandFunctions.php

15. There are now strong parallels of interest (specifically Chlamyida Pneumonia and Mycoplasma) that have emerged between the current work and that of prominent research on the so-called "Gulf War Syndrome". Additional parallels of interest occur with such conditions as Lyme Disease, fibromyalgia and Chronic Fatique Syndrome.

16. The structure, chemistry and internal composition of the biological based filaments appears at this stage to be essentially identical to that of the cultured filaments. This offers the distinct advantage that numerous research projects can now be pursued within a controlled laboratory environment, including that of growth inhibition.

17. It is understood that there are likely many numerous variations of development, form and manifestation with respect to the " Morgellons" condition. This researcher has focused on, and continues to focus on, those elements that appear to exist as a common denominator in most (or all) subjects, regardless of any external symptoms that may or may not be present. It remains the assessment of this researcher that the blood (and the alteration of it) and the existence of certain filament forms (INTERNAL to the body) are central to the condition. The existence of skin anomalies does not appear to be, in any way, a suitable criteria for establishing or denying the existence of the condition. Thus far, essentially any individual that has been studied displays, to a varying degree, the common denominators of blood anomalies and filament existence that are a basis of this report. Exceptions to this last statement in some fashion are presumed to exist (although not identified thus far) and they are an obvious desirable pursuit in the research.

18. Future immediate needs include a full protein and genetic analysis of the filament forms, cultures and components that have been repeatedly identified. Additional resources will be required to accomplish this.

19. Growth inhibition studies, especially upon the culture forms that have been developed, also exist as an immediate requirement. Preliminary studies with prospect are in progress. Additional resources can accelerate this process.

20. The available information indicates that the human condition is likely to have been affected en masse.

PHOTOGRAPHS:


Original previously analyzed dental sample material in wine base. Essentially all individuals tested thus far produce varying degrees of this dental filament material.


Representative dental sample material, previously analyzed, placed onto a glass slide. This particular sample uses a wine-hydrogen peroxide base mix.

The culture of the dental filaments at the early stage. Characterised by a pure white color. Micrsocopic and time lapse imagery of this development are available in more detail in the papers entitled Culture Breakthrough (?), (Jul 2008), Culture Work is Confirmed (Aug 2008) and Morgellons : Growth Captured (Aug 2008).


This is the culture material used in this test. This culture has been developed from extracted dental samples that have been placed within a red wine culture medium. The approximate time of development is approximately two weeks. The first stage of development is characterized by a pure white filament as shown above; subsequent stages will transform to a greenish color and ultimately to a deep black color.


A close-up of the culture development to the left. This is typical of a culture in the mid to mature development stage. Folding with the developed culture is common during maturation. Growth and folding up to approximately 3/4" to 1" has. been. observed, apparenly only restrained by the lid of the culture dish and the available growth medium.


Decomposition of the fillaments, either biological or cultured, involves the use of an alkali solution and heat. Currently, the filaments are placed within approxmately 1-2 ml. of distilled water with a drop of concentrated sodium and potassium hydroxide added. The concentration of the base can be determined at a later point; it does not appear to be critical at this stage. Initial decomposition takes place along with a transformation of the solution to a blackish color. The addition of heat, to the boiling point, appears to be an additional critical factor in the decomposition process. The addition of the strong alkali and the additional heat will turn the final solution to a deep red color (visually similiar to that of blood in solution). If the solution is made in a concentrated form, i.e., limited water, the subsequent examination of components under the microscope will be faciliated.


An erythrocytic form that appears from within a cultured filament after decomposition by chemical and thermal processes.. Varying degrees of reconstitution occur.. Reconstitution is not complete in all cases, and thus varying final diameters will occur. The source form appears to be on the order of four microns in diameter; the average of a final reconstitued erythrocytic form is on the order of 6-8 microns. This is also the diameter of a human erythrocyte. Biconcavity is a distingquishing visible characteristic. The fact that reconsitution of biological structures occurs within a hostile chemical and thermal environment is a primary topic of interest in the research.
Magnification approx. 8000x.


Direct evidence of decomposition of a cultured filament when subjected to alkali and heat. On numerous occasions, a breakdown in the bounding structure of the filament has been observed. The black arrow points to the boundary of the filament, which measures on the order of 15 microns in width. The blue circle encloses an erythroytic form in an early stage of reconstitution. Magnification approx. 8000x.


Additional direct evidence that the erythrocytic form are contained within the fllament forms. Another example of the breakdown of the filament boundary when subject to an alkali and heated solution. A series of erythroytic forms, prior to reconstitution, are visble emanating from the filament. Magnification approx. 8000x.


An internal component of a decomposed (alkali and heat) cultured filament. A reconstituted erythrocytic form with the intracellular sub-micron spherical structure visible (black arrow). Chlamydia-like, especially Chlamydia Pneumonia, organisms are primary candidates of consideration in the future identification of this structure. Speciallized modifications to any original biological form, should it be identified, are anticipated. Magnification approx. 8000x.


An internal component of a decomposed (alkali and heat) cultured filament. Another example of the intracellular sub-micron structure within an reconstituted erythrocytic form (blue circle). This phenomenon occurs frequently in observation, and is identical to that observed in the anomolus human blood observations reported on this site. The structure on the right edge appears to be an erythrocytic source form prior to reconstitution.
Magnification approx. 8000x.

Internal component of a decomposed (alkali and heat) cultured filament. Several examples of the sub-micron structure (black arrows) occuring within apartially reconstituted erythrocytic form. In human examples studied thus far, the damage to the integrity of erythrocytes appears to occur in direct proportion to the prevalence of the Chlamydia-like structure shown above. Magnification approx. 8000x.


The Chlamydia-like structure isolated and in detail. Numerous criteria (e.g, intracellular, size, Gram-Stain, symptomology, etc) suggest the Chlamydia-like organisms as a primary candidate for identification. Positive tests and additional resources will be required for completion of this stage of the research. In addition, this photograph shows the structures subjected to a Giemsa staining process (methylene blue and eosin). Chlamydia structures are expected to accept the blue stain under this test. This additional test is positive in this case, and further solidifies Chlamydia-like organisms as candidates for positive identification. The best size assessment thus far for this structure is on the order of 0.7-0.8 microns; also within the primary range of consideration for Chlamydia-like(esp.ChlamyidaPneumonia) organisms.
Magnification approx. 8000x.


A CONTROL photograph of human erythrocytes for comparison of size, geometry and biconcavity. A modified conventional analog micrroscope is used in this research; these modifications include the substitution of a digital camera chipfortheeyepiece (CCD) and a barlow lens to increase the magnification levels. Magnification approx. 8000x.


Additional examples of clusters of the Chlamydia-like structures that have been subjected to a Giemsa stain process. This stain process is damaging to the reconstituted erythrocytic forms, but it is helpful to accentuate the observation of the sub-microns structures as shown in this photograph. Human blood observations have shown identical forms under numerous occasions, and the severity of the so-called Morgellons condition appears to occur in proportion to the presence of this organism..
Magnification approx. 8000x.


An additional example of the Chlamydia-like structures that have been subjected to a Giemsa stain process.
Magnification approx. 8000x.


This photograph is unique and important in the fact that it represents the first successful complete cycle of the filament culture process.

The sequence of culturing is as follows:

1. Biological dental filament sample is extracted.
2. The biological filament sample is subjected to the alkali and heat process.
3.
A single drop of the resulting decomposed filament in solution is placed into a wine medium culture.
4. The resulting culture now develops through the following sequence:

a) Chlamydia-like organism develops first at the bottom of the solution over a period of a a few days.. This appears as the darkened, more diffuse form shown in this petri dish.
b) The pleomorphic, or tertiary form (ribbon-like) appears gradually over the next few days as well, also at the bottom of the wine medium. One candidate for identification of this form is mycoplasma.
c) The final stage is the development of the filament form on the top of the wine medium as is visible on this photograph. The initial development of the filament will be pure white; it will eventually transform through green and black stages at maturity.

It can be concluded that a single drop of the cultured solution (decomposed filament) is sufficient to reproduce the entire growth cycle of this pathogenic form.

The ring like distrubance in the central fluid portion of the petri dish is due to a copper sulphate inhibition study that is in progress. .


A filament culture in a wine medium, well developed, in the mid-level stages of development. The filaments will progress though a stage of pure white, green and subsequent black color, usually over a period of a couple of weeks.

An example of the pleomorphic, or tertiary form (ribbon-like) accompanied with a Chlamydia-like structure in the right central portion of the photograph. These forms develop in the culture sequence as described previously. These are the two most common forms also identified in the numerous anomalous blood observations that have been reported on extensively within this site. Magnifcation approx. 10,000x.


An example of what appears to be a developing filament form within the latter stage of the culture sequence described immediately above. Examples of the Chlamydia-like structures are visible to the left (black arrows) and the pleomorphic, tertiary (ribbon-like) form (black arrow) is visible on the right. In addition, a coelescing and enveloping structure is visible that contains the identified components ; it possesses full similarity to the filament forms studied extensively.
Magnification approx. 8000x.


Back to Aerosol Operations Main Page
Carnicom Institute

From:
AEROSOL OPERATION
CRIMES & COVER-UP

http://www.carnicom.com/blood2.htm
Author:
Clifford E Carnicom
Oct 08 2009

Note: Please go to this website to see the pictures clearly.

No comments:

Post a Comment

esoteric



SUBTITLES IN ENGLISH, ESPAÑOL, PORTUGUÊS

Click upon the circle after the small square for captions

MUFON

How to Digitally Record/Video a UFO sighting:


Como registar digitalmente ou gravar um vídeo de um avistamento de um UFO:




Stabilize the camera on a tripod. If there is no tripod, then set it on top of a stable, flat surface. If that is not possible lean against a wall to stabilize your body and prevent the camera from filming in a shaky, unsteady manner.

Estabilize a camera com um tripé. Se não tiver um tripé, então coloque-a em cima de uma superfície estável. Se não for possível, então encoste-se a uma parede para estabilizar o corpo e evitar que a camera registe de maneira tremida e instável.

Provide visual reference points for comparison. This includes the horizon, treetops, lampposts, houses, and geographical landmarks (i.e., Horsetooth Reservoir, Mt. Adams, etc.) Provide this in the video whenever is appropriate and doesn’t detract from what your focus is, the UFO.

Forneça pontos visuais de referência para comparação. Isso inclui o horizonte, cimo das árvores, postes de iluminação, pontos de referência geográficos (como o Reservatório de Horsetooth, Mone Adams, etc) Forneça esses pontos no vídeo sempre que for apropriado e não se distraia do que é o seu foco, o UFO/a Nave.

Narrate your videotape. Provide details of the date, time, location, and direction (N,S,E,W) you are looking in. Provide your observations on the weather, including approximate temperature, windspeed, any visible cloud cover or noticeable weather anomalies or events. Narrate on the shape, size, color, movements, approximate altitude of the UFO, etc and what it appears to be doing. Also include any unusual physical, psychological or emotional sensations you might have. Narrate any visual reference points on camera so they correlate with what the viewer will see, and thereby will be better able to understand.

Faça a narração do vídeo. Forneça pormenores sobre a data, hora, local e direcção (Norte, Sul, Este, Oeste) que está a observar. Faça observações sobre as condições atmosféricas, incluindo a temperatura aproximada, velocidade do vento, quantidade de nuvens, anomalias ou acontecimentos meteorológicos evidentes. Descreva a forma, o tamanho, a cor, os movimentos, a altitude aproximada onde se encontra o UFO/nave, etc e o que aparenta estar a fazer. Inclua também quaisquer aspectos pouco habituais de sensações físicas, psicológicas ou emocionais que possa ter. Faça a narração de todos os pontos de referência visual que o espectador irá ver e que, deste modo, será capaz de compreender melhor.

Be persistent and consistent. Return to the scene to videotape and record at this same location. If you have been successful once, the UFO sightings may be occurring in this region regularly, perhaps for specific reasons unknown, and you may be successful again. You may also wish to return to the same location at a different time of day (daylight hours) for better orientation and reference. Film just a minute or two under “normal” circumstances for comparison. Write down what you remember immediately after. As soon as you are done recording the experience/event, immediately write down your impressions, memories, thoughts, emotions, etc. so it is on the record in writing. If there were other witnesses, have them independently record their own impressions, thoughts, etc. Include in this exercise any drawings, sketches, or diagrams. Make sure you date and sign your documentation.

Seja persistente e não contraditório. Volte ao local da cena e registe o mesmo local. Se foi bem sucedido uma vez, pode ser que nessa região ocorram avistamentos de UFOs/naves com regularidade, talvez por razões específicas desconhecidas, e talvez possa ser novamente bem sucedido. Pode também desejar voltar ao mesmo lugar a horas diferentes do dia (durante as horas de luz)para ter uma orientação e referência melhor. Filme apenas um ,inuto ou dois em circunstâncias “normais” para ter um termo de comparação. Escreva tudo o que viu imediatamente após o acontecimento. Logo após ter feito o registo da experiência/acontecimento, escreva imediatamente as impressões, memórias, pensamentos, emoções, etc para que fiquem registadas por escrito. Se houver outras testemunhas, peça-lhes para registar independentemente as suas próprias impressões, pensamentos, etc. Inclua quaisquer desenhos, esbolos, diagramas. Certifique-se que data e assina o seu documento/testemunho.

Always be prepared. Have a digital camera or better yet a video camera with you, charged and ready to go, at all times. Make sure you know how to use your camera (and your cell phone video/photo camera) quickly and properly. These events can occur suddenly, unexpectedly, and often quite randomly, so you will need to be prepared.

Esteja sempre preparado, Tenha sempre uma camera digital, melhor ainda, uma camera vídeo consigo, carregada e pronta a usar sempre que necessário. Certifique-se que sabe como lidar com a sua camera (ou com o seu celular/camera fotográfica) rápida e adequadamente. Esses acontecimentos podem acontecer súbita e inesperadamente e, por vezes, acidentalmente, por isso, necessita estar preparado.

Look up. Be prepared. Report. Share.

Olhe para cima, Esteja preparado, Relate, Partilhe.

MUFON.COM

ESOTERIC



Pf., clique no símbolo do YouTube e depois no quadrado pequeno, em baixo, ao lado direito para obter as legendas CC, e escolha PORTUGUÊS

埋め込み画像 4埋め込み画像 5

What time is Around the World?

Translate

AND YOU AND I - click image

JAIL THE BANKERS

ET CONTACT MEDITAWTION

NGC - UFO's in EUROPE (Porugal included)

FEBRUARY 7, 2013 - 7:00PM EST

FEBRUARY 7, 2013 - 7:00PM EST
T O R O N T O