A site ive posted n spoke of often(a site for RSD) -thought id share for the ''newbies''or anyone interested

[Guest guest]

Hi all,

Ive come across ALOT of websites in the past 6 +yrs of my having RSD...some

have been filled with lies and what i call scare tactics. I remember going

into my drs office back in 2001 with my mother completely hysterical and

freaking out- showing him pages we had printed out. He threw them down and

said we have to be careful where we get info on the internet.

this one site I LOVE and am a member with/get newsletter and know the owner

is incredible, its an rsd association based in my home state of

Connecticut.

please look around , send to friends and family and I pray that maybe itd

help offer some info and understanding.

Luv

http://www.rsds.org/index2.html