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LDN for CFS

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I am new to the group and, like Jim and Beth, am interested in LDN

for ME/CFIDS/FMS. I'm so glad they both posted.

I have been ill for over 20 years and was bedridden for 3 years. I'm

just learning about LDN and trying to gather as much info as possible

before approaching my doctor. I also live in Ontario Canada and when

it comes to health issues, most of our doctors are extremely

conservative. We are well behind you guys.

I notice on the ProHealth Board posting " Is Anyone Using Low-dose

Naltrexone? " , the person mentions clinical trials going on

specifically for FMS as well as MS. Does anyone know to which she

refers as I have been unable to uncover anything in my research.

Thanks to Beth and Lori for their messages of welcome and support.

Thanks to all for sharing your knowledge and experiences to benefit

others.

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