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Question to the Lyme patients

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I have noticed quite a number of group members have found out they have Lyme or

Lyme-induced MS. What I am wondering is what is the treatment you are doing? I

assume it is long term and alternating of antibiotics? Also what is the outcome?

Are you getting better from the Lyme treatment with antibiotics or other Lyme

treatment?

The reason I ask is that I am not sure it is worth it for me to spend the money

on specialized Lyme testing given that I don't think I would want to take the

antibiotic treatment regimen.

Thanks for any input.

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