rsd

does anyone here have rsd? i have had rsd for almost ten years now. i am in almost all the time. actually it is all the time. i have tried different treatments and meds. i just wander if anyone else has rsd?

yes I also have had RSd for almost 9 years. mine effects both my legs from toes to hips. I know it is so hard and for me at least it has even almost completly destroyed my now 4 year marriage. I am on and off the computer usually all day as I had to stop working back in 2003 as a result of all the wonderful medication side effects and just functioning with all the pain in general. Feel free to email or IM me anytime. often I will not show as on my yahoo but am actually on so just drop me a line.

Blessed Be
Deb

RSD is not whom we are but rather just a part of us and not the best part!

Wow! I was suprised to see the words RSD nobody knows what this is I was diagnosed with it about 8 years ago in my hand from a severe crush injury that was diagnosed incorrect. I'm new to the board as I have said in other post I belong in so many areas. I also have been recenly diagnosed with Psoriasis 80% so I truly understand the pain and suffering of many
illnesses. I'm here if anyone needs to talk I'm usualy up all night and not able to sleep so for those who need to chat in the wee hours I just want to say I'm here.