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Re: EDS & Nutrition

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Hi Pam, Welcome to our group! This is Cindy C. We have talked before. I have

seen the site, and surfed around it several times. I found it very interesting.

Probably time for me to read it again. Glad to see you found us. Ask anything

big or small, and we'll try to help. Cindylouwho

From: Pam B To: ceda

Hi everyone.. I'm new to this... I haven't been officially diagnosed w/EDS,

but I have many of the symptoms associated w/type III.

But I've been doing a lot of research. And I was wondering if anyone has read

the following website devised by a women who has linked EDS & other connective

tissue disorders, Fibromyalgia, etc. with not only genetics but also nutrition.

It's a very comprehensive & extensive website. But I found it very interesting.

I'm sure some, if not all of you have seen this website, but just in case here

it is: Thanks, Pam Brewer

http://www.ctds.info/index.html

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