Guest guest Posted July 5, 2008 Report Share Posted July 5, 2008 Hi everyone - Through so many recent posts I've learned tons (thank you Limin) but now find myself wondering what should I be doing next? If someone suspected Lyme in their child with autism what do they do first? Second? Third? It's as overwhelming to me as three years ago when starting biomed in the first place. Only this time the hard-to-test critter is borrelia, not mercury. So since our Western Blot test was inconclusive (only positive for 41d)... what now? I thought using some Nutramedix products and doing a urine pcr test (for corpses, right?) would be more conclusive? It's hard for me to say whether Evan has " symptoms " of Lyme... he's totally nonverbal. I don't know what aches or pains him. But he's a total nonresponder to biomed, his immune system is pretty poor (obviously heavy metal toxicity impacts that) and he's broken out in the bullseye rash (unusual, I know) a couple months ago after starting homeopathy. I'm not sure if our homeopathic treatments caused the reflare or what. If he does have Lyme I assume he got it in utero because I have lots of symptoms but have never tested myself. So what now? Do I do more testing? Do I find a practitioner first (any ideas on that?)? Do I redraw the Igenex test now that I've done 10 days of NutraMedix herbs even though I wasn't using them properly? (Limin - I appreciate the detailed explanation of those herbal remedies in your last post. Thank you.) Or do I just throw in the towel? My brain is starting to get exhausted. I say that without meaning to sound ungrateful for everyone's feedback so far - you've been wonderful. But I still don't know what to do next! Thanks in advance, Dawnmarie Quote Link to comment Share on other sites More sharing options...
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