If you are still looking, please let us know more about what your friends are looking for: eg. location, price range (since most LLMDs don't take insurance), and any other helpful info.
Posts: 408 | From California | Registered: Apr 2008
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lpkayak
Honored Contributor (10K+ posts)
Member # 5230
posted
i got a bunch and they say "thanks"
-------------------- Lyme? Its complicated. Educate yourself. Posts: 13712 | From new england | Registered: Feb 2004
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Kathy Boss
Frequent Contributor (1K+ posts)
Member # 3062
posted
Contact the CA lyme group.
They will give you lot's of info.
What part of CA do you live in?
Brooke Landau who is a news anchor out of San Diego has Lyme and is a wealth of information for support groups and doctors.
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/