OT: Anyone have any experience with the test My Lyme Immune ID?

[Guest guest]

I saw one gentleman on the boards who had the test, but have found plenty of

negative (though not first hand comments) generally on the web.

My functional medicine doc who's treating me for the mold illness and mercury

poisoning (the latter less effectively than the former) suddenly wants to run

this test after excusing herself from assisting me with the chronic Lyme a year

ago. It's almost $1000 out of pocket.

I've been using Buhner's protocol for year and starting coiling 2 months ago and

I've been taking small amounts of MMS trying to build up. I doubt I would be

having herxes to these healing protocols if I didn't have Lyme and/or friends.

I'd rather put the money into healing since I trust my diagnosis at this point,

unless that test is particularly good at pinpointing something that would yield

more precise guidance.

Anyway, back off to MGH to sit with my husband. Started having severe chest

pain only 4 months after the stent. They're suspecting undue scarring in the

stent is re-blocking, but the cath lab doesn't start up again until Monday, so

he's stable and bored. (I pointed out that he was also fortunate and blessed,

but he's a bit grumpy about the whole thing.) I was getting so behind at work,

because the stress and anxiety about something being wrong with the stent was

pushing the insomnia off the chart which augmented the brain fog. The last 10

days before this came to a head I was able to make great progress on an overdue

project thanks to the folks on the board who mentioned the really high doses of

the detox protocols---the Burbur, Pinella and that Jergins(sp) neuroxtoxII

product. I was not taking nearly enough. Can't recall the names of the

posters...can barely recall the names of the products... but THANK YOU so much

for sharing. I'll be able to concentrate enough to wrap a few things up this

weekend so I can be fully present for his surgery Monday.

Many thanks.

Best regards,

Fifi