lyme in Putnam
Frequent Contributor (1K+ posts)
Member # 11561
posted
thanks Tracy - what bart symptoms do you have?
-------------------- He took u to it, He'll you through Posts: 2837 | From NE. | Registered: Apr 2007
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
Oh boy, I will have to look at a Bart list to differentiate them from the others; it seems so many overlap. I can't always tell what is Bart, and what is Lyme, never mind what is Babs which I am waiting right now on test results....
Anyway, one thing I have that developed over the last six months or so is the sole of the feet pain. It's really weird, it feels like you have been on your feet all day and they ache, burn, and sting.
The new neuro LLMD I just saw thinks many of my symptoms may actually be bart related: fatigue, night sweats, loss of balance, pain, and rashes I get. I had tested positive for Bart a while ago on Quest, but current LLMD hadn't treated it yet.
The new consult LLMD felt Bart should be immediately addressed, and basically said all my symptoms that I think are Lyme could be mostly Bart. So we'll see!!!
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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sometimesdilly
Frequent Contributor (1K+ posts)
Member # 9982
posted
tracy-
sole of feet pain is classic bart.
for what that is worth.. Posts: 2507 | From lost in the maze | Registered: Aug 2006
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
Ahem.....I thought you went to bed HOURS ago, girl???!!!????
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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bettyg
Unregistered
posted
AND i'm here just checking up on you both !! somebody's got to do it; you 2 have some really good times on the board, and i just wanted to join you!
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
LOL Betty, join on in!!!
I hope by now Dilly is fast asleep! Hoping I am soon, though knowing you, you are just getting going!
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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