New to a community

Hey there I am not new to lyme or it’s co infections, but I am new to the group. I’m currently at the Lyme Center of New England and I see you Sue but I do not feel like I’m being heard or treated correctly I’m on Zithromax and mepron I’m not too sure that it’s working at all I’m looking for an llmd that’s near to me I live in Fall River Massachusetts, I’m just looking for somebody who’s understanding caring can help me with supplements because she doesn’t even believe in them . Just need all around help

Snowisis – on the left hand side of the Home page about half way down is a link to Complementary Therapies – these are posts from community members about other things they’ve done to help themselves. You might find some good (or at least interesting) info there.

azurelle