T would like to know more about the group? ____________________________________________________________________________________ Never miss an email again! ...
-Hi Bill,My name is Regina and I joined the group a couple weeks again.First thanks for having me.I was told I had RSD almost 2 years ago and really didn't...
My name is Regina Cummings, and i'm so happy to say that I have found a group that I can relate with.About 1 year and a half ago I was told that I have RSD...
Looking Nudist friends and soul mates to share the clothes free life style ? This is the Best and Largest Personals network for Nudist&Naturist singles ! Join...
Hi, new here. Injured Dec 2, 06 and diagnosed last Wednesday. People and reading websites state I am lucky to have discovered it so soon. However, how soon is...
Welcome! There isn't much action here, unfortunately. I just wanted to let you know that what you read on the web can sometimes paint a very bleak picture of...
Dearest Friends, I am writing to let you know that a friend and fellow RSD member died last Saturday night. Stacy Johansson (aka, Blue Angel) was diagnosed...
It might really help you to join this online forum for people with RSD: http://neurotalk.psychcentral.com/forumdisplay.php?f=21&order=desc You can ask any...
Dana, I have a group that has a lot of info to help you. It's at - http://www.care2.com/c2c/group/No_Pain The group is free to join. I have RSD now for seven...
Hello everyone, I'm new to this group. I had RSD and recovered from it 8 years ago when I was 13 years old. Although we called it Reflexive Neurovascular...
Hi there, my name is Regina and i'm very happy to meet u. No the group is not very active, no 1 seems to be on when I come to thr site, maybe u will have...
Well, here is a real good, active group: http://neurotalk.psychcentral.com/forumdisplay.php?f=21&order=desc Many experienced RSDers there to anwer questions!! ...
yes, check us out. From: Smith Vanessa <missvanessalynn16@...> Reply-To: RSD_LINKS@yahoogroups.com To: RSD_LINKS@yahoogroups.com Subject: RE: [RSD_LINKS]...
... THE QUESTION I WOULD LIKE TO ASK IS, WHY IS THERE NOT ANY RESEARCH BEING DONE ON THIS DISEASE IF IT IS AS DRASTIC A LIFE CHANGE AS IT IS FOR THE SUFFERERS?...
There is all kinds of research being done. right now in Germany and Mexico they are trying a way to "reset" the nervous system by putting the patients in a 5...
I sustained an injury (work related) to right ankle Feb 12th 2007. I have to fractures and of course torn ligments and tendons. One tendon ripped chip of bone...
I have two fractures (talus and calcanus), thus the need for bracing. I do not wear the brace at home whie doing simple things. I only wear if up for long...
RSDSA has printed the I have CRPS card. It's a tri- fold card that contains a description of CRPS from the point of view of a person with the syndrome and some...
Having problems with message search?
Fill out this form to ensure your group is one of the first to be migrated to the new message search system.
