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◄Mycoplasms�?/A> : TESTING FOR MYCOPLASMA IN YOUR BODY
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Reply
 Message 1 of 3 in Discussion 
From: Rene  (Original Message)Sent: 4/12/2006 9:06 PM
 

 

VI - TESTING FOR MYCOPLASMA IN YOUR BODY

Polymerase Chain Reaction Test

Information is not generally available about this agent because, first of all, the mycoplasma is such a minutely small disease agent. A hundred years ago, certain medical theoreticians conceived that there must be a form of disease agent smaller than bacteria and viruses. This pathogenic organism, the mycoplasma, is so minute that normal blood and tissue tests will not reveal its presence as the source of the disease.

Your doctor may diagnose you with Alzheimer's disease, and he will say: "Golly, we don't know where Alzheimer's comes from. All we know is that your brain begins to deteriorate, cells rupture, the myelin sheath around the nerves dissolves, and so on." Or if you have chronic fatigue syndrome, the doctor will not be able to find any cause for your illness with ordinary blood and tissue tests.

This mycoplasma couldn't be detected until about 30 years ago when the polymerase chain reaction (PCR) test was developed, in which a sample of your blood is examined and damaged particles are removed and subjected to a polymerase chain reaction. This causes the DNA in the particles to break down. The particles are then placed in a nutrient, which causes the DNA to grow back into its original form. If enough of the substance is produced, the form can be recognised, so it can be determined whether Brucella or another kind of agent is behind that particular mycoplasma.

Blood Test

If you or anybody in your family has myalgic encephalomyelitis, fibromyalgia, multiple sclerosis or Alzheimer's, you can send a blood sample to Dr Les Simpson in New Zealand for testing.

If you are ill with these diseases, your red blood cells will not be normal doughnut-shaped blood cells capable of being compressed and squeezed through the capillaries, but will swell up like cherry-filled doughnuts which cannot be compressed. The blood cells become enlarged and distended because the only way the mycoplasma can exist is by uptaking pre-formed sterols from the host cell. One of the best sources of pre-formed sterols is cholesterol, and cholesterol is what gives your blood cells flexibility. If the cholesterol is taken out by the mycoplasma, the red blood cell swells up and doesn't go through, and the person begins to feel all the aches and pains and all the damage it causes to the brain, the heart, the stomach, the feet and the whole body because blood and oxygen are cut off.

And that is why people with fibromyalgia and chronic fatigue syndrome have such a terrible time. When the blood is cut off from the brain, punctate lesions appear because those parts of the brain die. The mycoplasma will get into portions of the heart muscle, especially the left ventricle, and those cells will die. Certain people have cells in the lateral ventricles of the brain that have a genetic predisposition to admit the mycoplasma, and this causes the lateral ventricles to deteriorate and die. This leads to multiple sclerosis, which will progress until these people are totally disabled; frequently, they die prematurely. The mycoplasma will get into the lower bowel, parts of which will die, thus causing colitis. All of these diseases are caused by the degenerating properties of the mycoplasma.

In early 2000, a gentleman in Sudbury phoned me and told me he had fibromyalgia. He applied for a pension and was turned down because his doctor said it was all in his head and there was no external evidence. I gave him the proper form and a vial, and he sent his blood to Dr Simpson to be tested. He did this with his family doctor's approval, and the results from Dr Simpson showed that only 4% of his red blood cells were functioning normally and carrying the appropriate amount of oxygen to his poor body, whereas 83% were distended, enlarged and hardened, and wouldn't go through the capillaries without an awful lot of pressure and trouble. This is the physical evidence of the damage that is done.

ECG Test

You can also ask your doctor to give you a 24-hour Holter ECG. You know, of course, that an electrocardiogram is a measure of your heartbeat and shows what is going on in the right ventricle, the left ventricle and so on. Tests show that 100% of patients with chronic fatigue syndrome and fibromyalgia have an irregular heartbeat. At various periods during the 24 hours, the heart, instead of working happily away going "bump-BUMP, bump-BUMP", every now and again goes "buhbuhbuhbuhbuhbuhbuhbuhbuh". The T-wave (the waves are called P, Q, R, S and T) is normally a peak, and then the wave levels off and starts with the P-wave again. In chronic fatigue and fibromyalgia patients, the T-wave flattens off, or actually inverts. That means the blood in the left ventricle is not being squeezed up through the aorta and around through the body.

My client from Sudbury had this test done and, lo and behold, the results stated: "The shape of T and S-T suggests left ventricle strain pattern, although voltage and so on is normal." The doctor had no clue as to why the T-wave was not working properly. I analysed the report of this patient who had been turned down by Canada Pensions and sent it back to them. They wrote back, saying: "It looks like we may have made a mistake. We are going to give you a hearing and you can explain this to us in more detail."

So it is not all in your imagination. There is actual physical damage to the heart. The left ventricle muscles do show scarring. That is why many people are diagnosed with a heart condition when they first develop fibromyalgia, but it's only one of several problems because the mycoplasma can do all kinds of damage.

Blood Volume Test

You can also ask your doctor for a blood volume test. Every human being requires a certain amount of blood per pound of body weight, and it has been observed that people with fibromyalgia, chronic fatigue syndrome, multiple sclerosis and other illnesses do not have the normal blood volume their body needs to function properly. Doctors aren't normally aware of this.

This test measures the amount of blood in the human body by taking out 5 cc, putting a tracer in it and then putting it back into the body. One hour later, take out 5 cc again and look for the tracer. The thicker the blood and the lower the blood volume, the more tracer you will find.

The analysis of one of my clients stated: "This patient was referred for red cell mass study. The red cell volume is 16.9 ml per kg of body weight. The normal range is 25 to 35 ml per kg. This guy has 36% less blood in his body than the body needs to function." And the doctor hadn't even known the test existed.

If you lost 36% of your blood in an accident, do you think your doctor would tell you that you are alright and should just take up line dancing and get over it? They would rush you to the nearest hospital and start transfusing you with blood. These tragic people with these awful diseases are functioning with anywhere from 7% to 50% less blood than their body needs to function.

VII - UNDOING THE DAMAGE

The body undoes the damage itself. The scarring in the brain of people with chronic fatigue and fibromyalgia will be repaired. There is cellular repair going on all the time. But the mycoplasma has moved on to the next cell.

In the early stages of a disease, doxycycline may reverse that disease process. It is one of the tetracycline antibiotics, but it is not bactericidal; it is bacteriostatic--it stops the growth of the mycoplasma. And if the mycoplasma growth can be stopped for long enough, then the immune system takes over.

Doxycycline treatment is discussed in a paper by mycoplasma expert Professor Garth Nicholson, PhD, of the Institute for Molecular Medicine.15 Dr Nicholson is involved in a US$8-million mycoplasma research program funded by the US military and headed by Dr Charles Engel of the NIH. The program is studying Gulf War veterans, 450 of them, because there is evidence to suggest that Gulf War syndrome is another illness (or set of illnesses) caused by mycoplasma.

Excerpted from a much longer article http://www.nexusmagazine.com/articles/mycoplasma.html

 



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Reply
 Message 2 of 3 in Discussion 
From: ReneSent: 10/28/2006 5:50 PM
 

Virus - Tip of the Day

Tip of the Day for July 02, 2003

At this year's AACFS International Research and Clinical Conference, Dr. Dan Peterson of Incline Village, Nevada, described his experience with Human Herpes virus 6 (HHV6). Dr. Peterson stated that HHV6 subtype "b" is common in infants and has been associated with MS, while subtype "a" is highly associated with CFS. He studied 135 patients who had encephalopathic features (such as vertigo, headache, and neurocognitive symptoms) and abnormalities on both MRI and SPECT scanning. 29 of these subjects had viruses identified in their cerebrospinal fluid: EBV (1), CMV (1), and HHV6a (27), but none had HHV6b, 7 or 8. Treatment with the antivirals valcyclovir and gangcyclovir were unsuccessful. However, on intravenous foscarnet 8 subjects improved and 4 were able to return to gainful employment.

(Source: AACFS 6th International Research and Clinical Conference - excerpted from Dr. Charles Lapp's summary of the conference.)

http://www.immunesupport.com/news/98sum006.htm

 http://www.hhv-6foundation.org/index.html

http://www.hhv-6foundation.org/testing.html

 

Patty Tam, Ph.D. and Ronald Messner, M.D. are interested in how viruses and their interaction with the host affect the development of chronic rheumatic and autoimmune diseases. Molecular analysis of coxsackievirus strains has identified the genetic determinants that cause chronic autoimmune myositis following infection. In a second project, second harmonic generation imaging technology that is used to detect changes in diseased muscle is being adapted to perform non-invasive imaging of the collagen found in knee joints. This project represents an interdisciplinary effort headed by Tam that includes investigators in dermatology, chemical engineering, and materials science; the Biomedical Image Processing Laboratory; and physics. The ability to detect minor degenerative changes in collagen on the cartilage surface will translate into earlier diagnosis and improved opportunities for therapeutic intervention in joint diseases such as osteoarthritis.

 Finally, in collaboration with other faculty in the Autoimmunity group at the University and faculty at the Mayo Clinic, Peterson is looking for clues to the patho­genesis of human psoriatic arthritis. He is using microarray technology to probe gene expression profiles in peripheral blood of patients with this disorder.


Research in the Tam laboratory
Enterovirus infection has been linked to the development of a number of chronic diseases including dilated cardiomyopathy, type I diabetes, and muscle diseases such as myositis and chronic fatigue syndrome. Investigations by Patty Tam are focused on a mouse model of chronic muscle weakness and myositis induced by myopathic coxsackievirus infection. The development of amyopathic virus variants that cause a typical acute infection but are attenuated for the later development of chronic muscle disease has led to reverse genetics studies to map the viral genetic determinants that control disease development. As many as five genetic differences between myopathic and amyopathic viruses appear to be involved, and some of these determinants may interact with each other. The location of these determinants within the viral genome has paved the way for future studies to explore their effects on viral tropism, persistence, and the host immune response to virus. These studies will lead to a better understanding of the mechanism by which enterovirus infection triggers the development of chronic muscle disease. They may also identify viral determinants that can be used to improve molecular epidemiologic studies. A second project is based on reports of persistent enterovirus RNA in the blood and/or muscle of patients with diseases such as chronic fatigue syndrome and fibromyalgia. Although enteroviruses possess a single-stranded RNA genome, studies in this laboratory have shown that viral RNA persists in muscle as a double-stranded molecule (dsRNA). This project explores the hypothesis that low-level persistence of viral dsRNA induces specific cellular stress-response pathways and is directly pathogenic for muscle, even in the absence of infectious virus. Cellular and mouse models of regulated transgenic expression of viral dsRNA are being developed to explore the nature of muscle pathology and identify a diagnostic signature for disease mediated by persistent viral dsRNA.

From   http://www.med.umn.edu/rheum/home.html



Reply
 Message 3 of 3 in Discussion 
From: ReneSent: 10/28/2006 5:51 PM
 


 LABORATORY TESTING INTRODUCTION 


Mycoplasma's are intracellular organisms that are extremely small, have pleomorphic characteristics (change shape and structure), lack rigid and distinctive cell walls and have unusual growth cycles and growth requirements (a semi-hibernation state for prolonged periods). This makes testing for Mycoplasma's much harder and more complicated than testing for all other bacteria.

Because the Mycoplasma is intracellular, the immune system does not readily produce antibodies (proteins made by a white blood cell as a primary defense against foreign substances, like IgG, IgM, etc). An antibody response has been demonstrated, but usually not until the disease has progressed.

Accurate diagnosis of Mycoplasma is complicated because mycoplasma is one of the few major bacterial pathogens of humans that can not be cultivated in vitro (or outside the body-- grown on a culture dish). Because of their extremely fastidious nature and the lack of reliable means for cultivation on artificial media, detection of these Mycoplasmal organisms rests primarily with molecular techniques.

The most reliable molecular technique offered today is with a lab test called a PCR test (Polymerase Chain Reaction). PCR, one of the most significant advances in DNA and RNA-based technologies, is a powerful tool enabling laboratories to detect a single gene of an infectious agent in any body fluid with improved accuracy and sensitivity . However, performing a PCR lab test on a standard whole blood sample may not even find the Mycoplasma, simply because it may be residing in other fluids and tissues in the body and not the blood (i.e.; the fluid in the joints, in the spinal fluid, or in any tissue cell or organ). A PCR test is usually done to detect each Mycoplasma species. These individual laboratory tests can be expensive, but are insurance reimbursable if ordered by your primary care physician.

These ultra-sensitive and ultra-specific Mycoplasma PCR tests can only be done by a small number of laboratories, and most university or government labs that have been specifically trained under a U.S. government contract.

MYCOPLASMA PATHOGEN SPECIES

Mycoplasma fermentans incognitus
Mycoplasma pneumoniae
Mycoplasma hominis
Mycoplasma genitalium
Mycoplasma penetrans
Ureaplasma urealyticum

(Created 7/1/05 by Sharon Briggs), ©2005 Mycoplasma Support All Rights Reserved Revised 9/23/05

 

TESTING GUIDELINES

INSTRUCTIONS FOR ACCURATE AND RELIABLE PCR TEST

Do not take any antibiotics for at least one month or more before a PCR blood test. The antibiotics will remove most of the infection from the blood, preventing an accurate result. This restriction also applies to natural products that kill Mycoplasmas,

The best time to have blood drawn is when an individual is symptomatic. Mycoplasma can remain in a semi-hibernation state and not cause symptoms. When the individual has symptoms, the Mycoplasma are more likely to be circulating in the blood.

Have the blood drawn at the testing lab. If that is impractical, have the blood drawn at a local lab and delivered to the testing lab by courier (i.e., Fed Ex) within 24 hours.

Have the blood sample drawn later in the day if you are shipping by overnight courier.

Send the sample early in the week to insure that it will be processed promptly.

A PCR test can also be performed on tissue samples (bone marrow, thyroid gland, etc.) and on other fluids (cerebrospinal and synovial).

Specimen Requirements: one (1) 5 cc Lavender top Plastic Tube (EDTA). The blood, fluid or tissue is collected, immediately mixed and placed on blue ice. The specimen is then shipped on blue ice (avoid freezing sample) by courier to arrive at the testing lab within 24-36 hours.

(Created 7/1/05 by Sharon Briggs)

From:   http://www.mycoplasmasupport.org/Web_pages/Lab/lab_guide.htm

and more here, too:   http://www.mycoplasmasupport.org/