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[quote=Anonymous]20% of cases won’t resolve with initial treatment.  There are tests like TLab they can look for actual infection not antibodies as this will frequently make your immune system malfunction.  You need a Lyme literate MD now.  Fwiw I was a doctor, misdiagnosed for years until it got very bad and now I’m trying to get better.  Local providers are a bit all over the place.  Jemsek is probably most experienced local provider.  You’ll find some people use combos of antibiotics pulsed, some use rife machine, some use herbals.  I know this stuff looks like sci-fi garbage when you look it up.  Trust me when I say you sing a very different tune if you get sick enough.  The Washington post guy wrote a book of his experience that discusses some of this.  It’s very hard as there is no straight path to treatment because until extremely recently this was not acknowledged to be a persistent infection.  If you can get the folks in Columbia to pick up the phone they have a lot of active research up there.  I see a doctor in New York.   ILADS will give you a list of providers or some functional meds can at least tackle the first steps of treatment.   Have your family members evaluated.[/quote]

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