Lyme Disease: The CDC’s Greatest Coverup & What They Don’t Want You To Know

7 thoughts on “Lyme Disease: The CDC’s Greatest Coverup & What They Don’t Want You To Know

  1. hi – I can’t deny chronic lyme does not exist, I suffer myself from symptoms, some debilitating, and have been given numerous diagnoses along the years – fibromyalgia, CFS, DDD, chronic sinusitis, chron’s. The one thing I don’t understand is why would they cover up and illness like chronic lyme disease? If they do cover it up then the insurance companies have to pay way more for treatments for other chronic illnesses that are thought to be a result of chronic lyme disease. (MS, Lupus, ALS) The treatments for these diseases are WAY more costly compared to what insurance companies would pay for say .. an year of IV antibiotics? What’s the catch?

    I hope you get what I mean. Why would the IDSA hide chronic lyme and then the insurance companies have to deal with patients that have 5, 6, 12 other chronic illneses?

    1. Actually, by covering up the disease the insurance companies pay LESS for treatment. Always look for the profit motive, especially the profit motive that exists in a blood-sucking tick masquerading as an “insurance” industry. If the insurance middle man were removed an amazing transformation will be observed in the cost structure of American medicine. Just think of all the non-medical costs built in with this insurance rip-off. You can rest assured that your medical costs cover the buildings, actuarials, and vast quantities of middlemen employed by the insurance industry – quite a pretty penny! – g

  2. Rob,
    Please look for a LLMD in your area. If you live in CT and have ALS you absolutely need to make sure that you don’t have lyme. You very likely could have it. You can find an llmd through: http://www.iwww.ilads.owww.ilads.org
    Lyme is very commonly misdiagnosed as ALS 🙁 please see an llmd asap.
    Good luck,
    Katy

  3. hey … i have ALS in second year…. 52 year old male. Bulbar palsey. Is anyone willing to test me?

    I live in connecticut and have had Lyme antibiotics a few times…

    1. Really sorry to learn you’re a sufferer, Rob. Perhaps if you contact the author you might be able to get some test referrals. Thanks for commenting g

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