Re: EDS & Nutrition - Re Web Link

[Guest guest]

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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Pam -

Thanks much for posting this link. I don't have time right now to

review it in detail because I am trying to get the RV all loaded and

ready to hit the road for a couple of weeks starting tomorrow.

I did, however, have a chance to check a couple of the links within

the site for a quick and dirty cross check. Specifically, I checked

the link for Sciatica Treatment to see what it said. Is any one

suprised that I found it very interesting that she listed

acupressure as a viable treatment along with " Acupressure's Potent

Points " as a recommended reference source?

I added it to my list of favorites for review when I get back home

at the end of the month. Preliminary review, however, shows it to

be very detailed and well done. I definitely want to get into it

much more heavily when I get the time.

Again, thanks and good job.

Mike