I really appreciate all the sharing and support offered across this site!
Lyme has recently come up as a differential diagnosis for the several health problems I've had over the years. I've scheduled my first LLMD appt with Dr. S in SF per the advice of my neurologist, so hopefully I will know more soon.
Anyone know of any lyme groups in the Seattle area? If there are any that meet on the Eastside, that would be preferable.
I'd love to get connected with others locally who might be working through similar challenges.
Thanks!
Posts: 10 | From USA | Registered: Jan 2009
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posted
Anna, thanks so much for the info! I've signed up to join the yahoo group... pending approval now.
I'll PM you with more specifics on reasons for going to see an SF LLMD. Would be good to hear more on your Seattle LLMD experiences.
Thanks! -s
Posts: 10 | From USA | Registered: Jan 2009
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bettyg
Unregistered
posted
beating, your state is blessed to have 30-35 ll/lfriendly llmds! boy, what we wouldn't give in the midwest to have that many to chose from!
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