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Saturday, September 02, 2017

How AIDS blunders by the CDC’s Mary Guinan disguised the Chronic Fatigue Syndrome epidemic

Mary Guinan was one of the prominent early "AIDS" investigators at the Centers for Disease Control. This show explores the mistakes she made in the original epidemiology of "AIDS" that led to the mistaken separation of the "AIDS" and "Chronic Fatigue Syndrome" epidemics. This program also presents a discussion of a CDC employee named Gus Sermos who tried to blow the whistle on the shocking dishonesty of CDC AIDS researcher James Curran. Sermos was punished for trying to tell the world what was really going on at the CDC. Curran is now a celebrated Dean at Emory University.
Charles Ortleb's free book about Guinan can be found at
Charles Ortleb's definitive history of AIDS and Chronic Fatigue Syndrome, Truth to Power, can be purchased at Amazon.
The closing song "Hello New York, I'm back" can be heard on Spotify.

Dr. Joseph Brewer on HHV-6

Dr. Brewer's model for HHV-6 Disease

Scientific Literature in Review: Chronic Active Human Herpesvirus-6 (HHV-6) Infection: A New Disease Paradigm by Joseph H. Brewer, M.D.
by Deborah Cooper

(Editor’s Note: Occasionally we will review scientific literature that has strong significance for CFS and FM and related disorders. Many doctors and leading researchers into the causes of chronic immune disorders such as CFS and FM draw a strong correlation between HHV-6 infection and the development of these diseases. Joseph Brewer, MD has written an extensive report on the role of HHV-6 in immune disorders and provides in-depth analysis of current possibilities for the diagnosis and treatment of HHV-6 infection. What follows is a review of his main findings. To read the full text of Dr. Brewer’s paper visit:

According to Joseph Brewer, M.D., CFS is strongly associated with HHV-6. To a slightly lesser degree FM is also linked to the virus. In his paper, “Chronic Active Human Herpesvirus-6 (HHV-6) Infection: A New Disease Paradigm,” Brewer provides a thorough exploration of HHV-6 infection, and includes observations from his several years of scientific study of the virus and the diseases it may preempt.

Dr. Brewer is part of a group of doctors who have studied HHV-6 intensively for the past two years. He writes in the introduction to the paper, that: “Based on the studies and observations in our own patient population…it is our belief that this virus can establish a chronic active infection in certain patient populations and lead to chronic diseases via several different postulated mechanisms.”

HHV-6: types of triggers

Brewer proposes several reasons why HHV-6 leads to chronic immune dysfunction. First, he points to a ‘triggering event’ where the latent HHV-6 virus is reactivated in the body. “The immune dysfunction presumably relates to cell mediated immunity (CMI) and natural killer (NK) cell dysfunction.” In this case, he writes, NK function is crucial to controlling the spread of the virus, because with loss of NK function may then lead to active HHV-6 infection.

Brewer’s research indicates several primary triggers for chronic immune dysfunction, arising from the HHV-6 virus. These are: CMI, genetic predisposition, active HHV-6 infection, chronically active HHV-6 infection, immune cell tropism, HHV-6 infection of the endothelial cells and neurotropism

Diagnosis of HHV-6 virus

Although testing for latent HHV-6 infection is considered to be straightforward and accurate the same cannot be said for detecting active HHV-6 infection. Brewer reviews the nuances of several currently available tests and concludes that the most effective one is the rapid culture test. ‘This test…is the best current assay system for active infection and active/productive infection is of paramount importance in defining this disease process as well as clinical diagnosis.”

A rapid viral culture test, as described by Brewer, is one where the patient’s leukocytes are co-cultured with fibroblasts. This fibroblast layer is stained so that early active infection will show up. This method is sensitive in the range of 80-85% with specificity of nearly 100%. However, this test does not distinguish between HHV-6 variant A and variant B, and no such test is commercially available at the present time.

Treatment Options:

a) Anti-viral drug therapy

Brewer discusses the efficacy of several treatment options. The ‘tried and tested’ anti-viral therapy is thoroughly explored with a discussion of the different medications available such as acyclovir (Zovirax), ganciclovir (Cytovene) and foscarnet (Foscavir), among others.

b) Immune modulation

Brewer describes immune modulation, as “another attractive avenue for consideration.” He writes that interferon may provide one kind of mechanism for this kind of regulation. Interferon has anti-viral properties and could affect HHV-6. However, statistically significant studies have yet to be done in this area so that, in future, “defining the effect of interferon on HHV-6 will be an important area of research.”

c) Anti-coagulants:

Brewer reports that one study with heparin did produce symptom improvement in CFS patients. Several other studies showed that heparin blocked the activity of the HHV-6 virus by preventing it from attaching to cell surfaces. Another possibility Brewer proposes involves “blocking viral activation (antiviral agents or immune modulation such as TF) combined with anticoagulants (heparin or coumadin).” d) Transfer factor therapy

According to Brewer, transfer factor (TF) “has consistently shown efficacy in the prevention and treatment of viral infections. Studies reporting efficacy of specific TF have been reported with HSV 1 and 2 VZV, EBV, and CMV. TF has proven to be extremely safe with virtually no significant adverse effects.”

Brewer goes on to describe studies he has conducted in patients with CFS and chronic active HHV-6 infection using a TF specific for HHV-6. He reports seeing “significant symptom improvement, consistently negative HHV-6 blood cultures and marked improvement in NK function.”

Overall, Brewer regards transfer factor therapy as having substantial promise for the treatment of HHV-6 related disorders.

Another article on Brewer and HHV-6:

Breaking News on HHV-6 Virus , February, 2003

At the February, 2003 meetings of the American Chronic Fatigue Syndrome Association, Dr. Joseph Brewer, an infectious disease specialist from Kansas City, reported a double blind study in which he claimed improvement for two-thirds of persons with chronic fatigue syndrome, while persons taking placebo did not improve.

If Dr. Brewer’s results are valid, then this is the most important treatment breakthrough so far for CFS. Ironically, Dr. Brewer’s study has received little attention so far, perhaps out of fear that it is “too good to be true”. We won’t know for sure until more double blind studies are done to confirm his dramatic findings, or until enough patients try it and report their anecdotal results.

Dr. Brewer’s formal study focused only on that sub-group of CFS patients who had Herpes Virus-6 found on special culture. However, since HHV-6 can be present without showing up on culture, Dr. Brewer now believes that both HHV-6 positive and HHV-6 negative persons may respond. Dr. Brewer told me that he now treats all CFS patients with transfer factor, and that he believes his results for “all-comers” are just as good as in his study. Of course, the “all-comers” data is anecdotal experience, no longer double-blind.

Dr. Brewer identified 38 CFS patients who had a positive culture for HHV-6 Virus. Twenty eight received a capsule containing cow’s milk colostrums. The cow had first been specifically primed to make antibodies against HHV-6 virus. Ten patients, the controls, received standard colostrum, without special HHV-6 antibodies. Treatment lasted six months.

Based on symptom report scores 68% of people treated with anti-HHV-6 colostrum improved by 25% or more. In contrast, none of the “control” patients improved by that much.

For the HHV-6 treated patients the average symptom score decreased from 76 to 41. The control group’s average symptom score increased from 79 to 81. Natural killer cell function scores also improved in the HHV-6 treatment group from an average of 8 units to 54 units. Natural killer cell function for control patients did not change.

If Dr. Brewer’s observations are correct, this would be a major breakthrough treatment, at least for persons who have low grade chronic infection with HHV-6.

One problem: some healthy people also grow HHV-6 from their blood, so the mere presence of HHV-6 doesn’t necessarily mean that it’s making you ill.

Dr. Podell’s Perspective on Transfer Factor and HHV-6 Virus: Dr. Brewer’s treatment is probably very safe, so pending further data, it’s definitely worth a try. Some patients get a mild flu-like reaction when starting the treatment, but that seems to be worst side-effects. Most (but not all) people with cow’s milk allergy tolerate the colustrum. It costs $140 a month. Not cheap, but certainly worth it if the treatment works as claimed. Dr. Brewer feels that a three month trial would be reasonable to judge on.

Three Big Books

Two books on amazon

Everyone needs to know what the CDC is hiding about CFS and HHV-6. NEW YORK NATIVE contains both volumes of THE CHRONIC FATIGUE SYNDROME EPIDEMIC COVER-UP. The print version is $23. Only $7.98 in Kindle.

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