Interesting case for us Lyme folk.
Sound familiar? I sure hope they are treated with more respect and dignity than chronic LD patients are. They will call it: "Post Ebola Treatment Syndrome" P.T.E.S. right up there next to
P.T.L.D.S.!! (AKA: "Aches & Pains of Daily Living.") Are the Lyme-like symptoms (arthralgias etc) from local persistent Ebola or a result of remotely-triggered inflammation by sequestered localized ocular Ebola?
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