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About Me
clairejean
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Recent Activity
Today
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clairejean wrote a discussion post in the Lyme Disease support group: the treatment years 5:36am
Hi all, Almost to the end of my first year of tx. I'm now minimally functional on my best days. And that's…
November 9
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clairejean wrote a discussion post in the Lyme Disease support group: Vertigo and lyme 8:26pm
Hi all, Seems there is no rest from lyme! As soon as one symptom calms down, a new one flares up -- all…
November 7
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clairejean wrote a discussion post in the Lyme Disease support group: lyme and thyroid issues 4:36am
Hi all, i had some recent blood testing done to see how the lyme was affecting things and my throid t-3…
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Journal
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Prayer
Keep the Faith.
Congrats
So glad to read that your starting to see some real progress with your symptoms. I realize there are more sx to be addressed, but to me, the brain fogginess lifting was a HUGE first step. The physical improvements lagged behind the lifting of the brain fog; so hang in there, there is so much reason for hope!
Jenn-
Hug
Hi,
I'm also in Massachusetts. My Lyme doctor (a neurologist) is in Harvard MA. Is that far enough West for you? Let me know, and I can give you her name etc.
Jenn 
I’m With You
Hi, I've read your recent posts about lyme and herxing. Herxing can be so horrible! Do you have "lyme literate" doc (LLMD)? Some folks get better by going the natural route, but most seem to need heavy duty antibiotics for a while, when it's chronic lyme...and then, many "maintain" with herbs, supplements, etc. That's your call, though, of course! I do hope that you will feel much better very soon :)
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Support Groups
Close Pulmonary Embolism
hi, i had multiple pulmonary emboli on march 8, ion hospital 5 weeks and bedrest home five weeks - bararely getting back on my feet on blood thinner arixtra with bad side effects - need support thanks claiarejean
Close Lyme Disease
I have chronic lymes
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