BLOOD ISSUES INTENSIFY re Morgellons

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BLOOD ISSUES INTENSIFYClifford E Carnicom

http://www.carnicom.com/culture4.htm

Apr 16 2008This page is under development and is subject to revision. It will be completed as time and circumstances permit.

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.

Three independent methods have been established that appear to confirm the presence of developing erythrocytes (red blood cells) within cultured dental samples that exhibit the characteristics of the Morgellons condition as previously researched and identified. All individuals tested thus far have produced the dental filamentous materials, regardless of whether visible skin anomalies are present or not. Please see previous research for further clarification on the prevalence of the condition.

The erythrocytic detection methods are:

1. Direct observation under the microscope at relatively high magnification (8000x - 10000x) using developed microscopy techniques. 2. The use of the Kastle-Meyer presumptive test for blood, a method commonly used in forensics for blood identification. 3. The Hemastix (TMP) presumptive forensic test commonly used for blood identification.

The appearance of the cultured erythrocytic cellular structures, if accepted as properly identified, in and of itself defies all conventional understanding of blood cell development. This appearance also corroborates a long history of research througb this site of environmental and biological samples that defy conventional expectations and knowledge with respect to the state of public health and the environment (e.g, refer to Extraordinary Biological Observations, Carnicom, May 2004). Simply put, erythrocytes are not to be grown in the the test tube under the current state of conventional knowledge. To do so, however, is considered to be a holy grail of biological achievement with huge implications for bioengineering, human health and the human species. Ground breaking research in this aspect of biology, i.e, the "growing of blood cells" has been reported in the media throughout this last year, and was simultaneously stated to entice immediate interest from the Defense Department for battlefield applications (radio news report). Research previous to this recent announcement reports the sustenance and perpetuation of existing cells within a growth medium, but not the creation of new cells. Achievements of growth on any scale are clearly on the leading front of stem cell research, and comparative questions must be raised regarding the state of public disclosure on the subject vs. actual technological achievements that may already be in place.

I have no desire to sensationalize this subject as the seriousness of the issue is apparent to those that understand the ramifications of this report, should it bear itself to be true. I am obligated, however, to report on the state of affairs as they are encountered through honest research. I would hope that all three methods used here along with all previous reports involving erythrocytes for more than 10 years can be shown to be false, but if so, it will have to be done with open and public research that is subject to full cross-examination. I would prefer to not be forced to continue to report findings of this nature but the obligations with respect to public health and the environment do not afford me that liberty.

It has taken some time and effort for me to be able to employ three independent methods of erythrocyte identification at the forensic level, but the seriousness of the subject requires this as a minimum. I do not state this subject to be a closed affair, and quite to the contrary, I am opening a door that requests that there be additional resources activated to conduct the investigations in proper earnest. The purpose of this paper is not to incite controversy. It is to acknowledge what appears over and over to be a very real issue that appears to be of consequence whether we would like to confront it or not.

Now, for some of the specifics:

 

 

 

 

 

 

 

 

 

 

 

 

View of cultured dental sample #1subjected to Kastle-Myer blood detection forensic test. Peroxide activity characteristic of hemolysis and phenolphthalein color change to bright pink-red is evident. A positive presumptive test for the existence of blood within the cultured dental sample. On glass microscope slide. Magnification approx. 2x.

 

 

 

View of cultured dental sample #2 subjected to Kastle-Myer blood detection forensic test. Peroxide activity characteristic of hemolysis and phenolphthalein color change to bright pink-red is evident. A positive presumptive test for the existence of blood within the cultured dental sample. On glass microscope slide. Magnification approx. 2x.

 

 

 

 

 

 

 

 

 

Control case for the Kastle-Meyer presumptive blood detection test View of human blood sample subjected to Kastle-Myer blood detection forensic test. Peroxide activity characteristic of hemolysis and phenolphthalein color change to bright pink-red is evident. A positve test result On glass microscope slide. Magnification approx. 2x.

 

 

 

Second control case for the Kastle-Meyer presumptive blood detection test. No blood present in the sample. No peroxide hemolysis evident and no color change. A negative Kastle-Meyer forensic test result. On glass microscope slide. Magnification approx. 2x.

Summary : Both the human blood cell control test and the cultured dental samples produce the same visible physical and chemical reactions at the visible level and satisfy the expected conditions of blood detection by the Kastle-Meyer forensic test.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Microscopic view of human blood sample subjected to Kastle-Myer blood detection forensic test. Peroxide activity characteristic of hemolysis and phenolphthalein color change to bright pink-red is evident. Magnification approx. 600x.

 

 

 

Microscopic view of cultured dental sample #1subjected to Kastle-Myer blood detection forensic test. Peroxide activity characteristic of hemolysis and phenolphthalein color change to bright pink-red is evident. Magnification approx. 600x.

 

 

 

Microscopic view ofcultured dental sample #2 subjectedto Kastle-Myer blood detection forensic test. Peroxide activity characteristic of hemolysis and phenolphthalein color change to bright pink-red is evident. Magnification approx. 600x.

Summary : Both the human blood cell control test and the cultured dental samples produce the same visible physical and chemical reactions at the microscopic level and satisfy the expected conditions of blood detection by the Kastle-Meyer forensic test.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

HEMASTIX control blood test. The lower stick is that of a negative, i.e., no blood of any trace evident. The upper stick is a positive test that corresponds to one to two drops of human blood in 50 milliliters of distilled water. The HEMASTIX test is positive for the existence of blood essentially if any green to blue-green tint shows on the stick after a time interval of 60 seconds. The HEMASTIX test (TMB) is highly sensitive to the existence of blood in a sample. Magnification approx. 2x.

 

 

 

Positive HEMASTIX test result when exposed to dental culture sample #1. The sample is prepared by extraction of a small portion of the filamentous growth which is then placed on a glass slide. The sample is mechanically broken down with a scalpel and the HEMASTIX is exposed to the residual solution. The results are recorded at the stated time of 60 seconds. The cultured dental sample produces a positive test for the existence of blood. Magnification approx. 2x.

 

 

 

Positive HEMASTIX test result when exposed to dental culture sample #2. The sample is prepared by extraction of a small portion of the filamentous growth which is then placed on a glass slide. The sample is mechanically broken down with a scalpel and the HEMASTIX is exposed to the residual solution. The results are recorded at the stated time of 60 seconds. The cultured dental sample produces a positive test for the existence of blood.. Magnification approx. 2x.

Summary : Both the human blood cell control test and the cultured dental samples produce the same visible physical and chemical reactions and satisfy the expected conditions of blood detection by the HEMASTIX forensic test.

This page is under development and is subject to revision. It will be completed as time and circumstances permit.