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Dear Yankee

Updated Friday, October 12th, 2007

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3 Responses to Dear Yankee

  1. Lucy Barnes December 26, 2007 at 1:43 am #

    Imagine the audacity of a individual who feels it is acceptable to write a letter to Yankee Magazine in order to drum up business for himself and his medical colleagues at the expense of a well known, beloved and successful pediatrician who they have collectively tried to ruin both professionally and financially. Combine that lunacy with the fact that some of these self-absorbed block heads who declare themselves willing and able to take on this trampled doctor’s patients are already connected to a governmental investigation into illegal practices for possible fraud, anti-trust, monopolization and exclusionary conduct related directly to what they claim they are ?highly qualified? to do.

    My question- Would Larry Zemel (University of Connecticut School of Medicine, Farmington, CT) and his hand-picked cronies be more suited to be poster boys for the arrogant, the pompous or the narcissistic community?

    One thing for certain- They shouldn?t be allowed to treat ?sick or symptomatic children? with acute infections or the aftermath that follows. That is the last thing the Lyme disease community needs right now.

  2. Phyllis Mervine August 17, 2008 at 1:17 am #

    Dr. Zemel is correct, as far as he goes. There may not be a shortage of doctors treating “noninfectious” later symptoms of Lyme disease. However there WILL be a shortage of doctors treating the INFECTIOUS later symptoms of Lyme disease.

    Numerous peer-reviewed scientific studies document the resistance of Lyme disease to treatment and persistence of the Lyme spirochete in spite of much more aggressive treatments than Dr. Zemel is happy prescribing. Post-treatment symptoms are the norm because most cases are not treated adequately.

    Dr. Zemel relies on the guidelines of the Infectious Disease Society of America. These guidelines are currently being revised under strict conditions laid down by the Attorney General of Connecticut because the guidelines panel was corrupted by commercial conflicts of interest.

    Please visit for frequent updates on the revision process and order the summer issue of the Lyme Times to read about it.
    Phyllis Mervine, Pres.
    California Lyme Disease Assn.

  3. Donna Zuk August 20, 2008 at 12:48 am #

    I always wondered why rheumatologists take care of “fibromyalgia” patients. Fibromyalgia is suspected to be none other than undiagnosed, untreated or poorly treated late stage Lyme.

    Lyme has been found to have many coinfections which include mycoplasmas and fibromyalgia has also been found to have 3 types of mycoplasmas–fermantans, pneumoniae, genitalium–3 of which Eva Sapi, of the University of New Haven has found in Lyme.

    What do these rheumatologists do? They give you a psych exam, and then tell you you have ‘atypical rheumatoid arthritis’ and fibromyalgia (and send you to a neurologist who does the same) because they do not want to admit it is Lyme.

    The Western Blot is frequently negative because they use a GERMAN strain, not an American strain. There are 300 strains of Barrelia Burgdorferi– 100 of which are in America, yet they use a German strain. It only tests for that one strain, and does not test for any of the other co-infections that come along for the ride with Lyme

    In addition, many late Lyme sufferers don’t have enough antibodies to be detected on the Western Blot. If you get a test done on Polymer Chain Reaction (PCR) and get a positive result, the CDC will not add your Lyme to their statistics (Although they accept a positive PCR on cattle who have mycoplasmas and treat them with antibiotics. Oddly, only when it pertains to animals do they admit it is hard to treat. They also admit –when it’s cattle– that if the antibiotic is not strong enough, it is only bacteriostatic (stays the same, does not kill them) It is, in effect is only a temporary birth control for the little buggers, then they begin to multiply again as soon as the antibiotic is stopped.

    They attempted to have a vaccination for Lyme–Lymex– and used Osp A in the vaccine because it was so specific to Lyme. Osp A and Osp B are both specific to late stage Lyme, but they have removed them from the test, yet conveniently state late Lyme does nto exist. Removing the dinosaur footprints does not get rid of the dinosaur!

    Despite their stating they removed Lymex from the shelves because of lack of demand, the truth is, it was GIVING people Lyme symptoms.

    They’ve even tried, the worst of all sins, to get rid of colloidal silver, even lying about it, even trying to get it off the markets. But the fact is, it already has a patent, and it was used for infections WAY before chemical antibiotics were invented, and doesn’t create superbugs or kill your gall bladder. The blue man story was a man abusing it by drinking too much of his own homemade ionic batch. True colloidal silver is not ionic.

    The US has patents on mycoplasmas: US PATENT NO. 5,242,820 is one of them.

    US Law, the Ferres doctrine, gives them the right to experiment on the military:

    The government also has the legal right to experiment on “human subjects” aka citizens:

    The US CODE Title 50 chapter 32

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