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Lyme and Autism

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For those of you that have treated for Lyme, what protocols have you done? What

were the results? Adverse reactions?

My 4yo son with ASD was recently tested for Lyme by the labs at Stony Brook, NY

(supposedly one of the best) and Igenex. Results were virtually identical with

indication of chronic lyme (no co-infections luckily). Our integrative ped

neurologist recommends that we treat and suggested an herbal protocol (she

mentioned Cowden and someone else I can't remember). I am totally open to it as

we're tried many avenues and often see some initial improvement but then

backtrack. There seems to be a missing piece that we're not getting.

Anyway, back to my questions above. Experiences? Advice? Adverse outcomes?

Thanks,

Sylvia

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