I am starting a Lyme support group in Los Angeles. It will be confidential. I don't know where we will be meeting yet or when. But it will be most likely once every six weeks or so. Let me know if you are interested by replying to this message on this thread and where you would like me to contact you.
I will contact you with the details as soon as I know them.
Posts: 298 | From los angeles | Registered: Mar 2006
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bettyg
Unregistered
posted
lalyme,
have you checked out left side support groups?
here's california link to see what groups exist OR used to since the support group info is NOT UP TO DATE.
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
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