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, I live in an area that is not officially " endemic, " which means that

there are very few fellow Lyme patients who live near me. If there were

more, I'd form a support group. I, too, have felt so much worse with the abx

-- and have, as I told you in an earlier e-mail, periods of terrible,

suicidal depression. This group helps me a lot, but I do think it's

important to have someone to " unload " to, as you say. I think your having

written to the e-list and asking for help was not a burden to any one of us.

Most of us have felt at least some of what you're feeling. I guess you've

seen how many great, caring people there are on this list. Please stay with

us! I'm relatively new (just dx in May, started abx in June), and without

this group I'd be lost. I also have a wonderful therapist -- and I can

unload on her, too. Do you have a therapist? Friends are great and

supportive, but I think nothing can beat a good therapist/psychiatrist (the

latter could prescribe antidepressants if you would consider trying them).

My psych. didn't know a lot about Lyme when I was diagnosed but has actually

taken it upon herself to learn about the psychiatric/emotional aspects of the

disease. I'm very lucky. Anyway, I just wanted to say, again, that I'm

pulling for you. Hang in there, and hang in here with us. --charlotte in

vermont

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