New Memeber RSD/CRPS
 

Hello all, I have a daughter that has suffered with RSD for 14yrs she is now 21. She has suffered horrible with this condition. Her name is Ashley *edit*.
I also have RSD, not nearly as bad as most. They found mine within the first 4 months. I had 27 nerve blocks, trial SCS and now the pain pump. I don't talk a lot about my RSD, we all know how having one person with RSD goes with people judging and being rude. Just think how it goes when there are 2. We live in Calie and are always looking for others to help, support, and share.
*edit* We gotta stick together and find the answer to RSD.
Peace and less pain hugs.

Nice to meet you!!
 

:Wave-Hello:Hello and welcome to NeuroTalk. Happy to see you have come to be with us. Just let us know if we can be of any help.

There are great number and caring fellow members here, you will see we are supportive and relaxing place. Our shoulders are here for support in many ways.

Check into the following for some assistance.

SCS & Pain Pumps:
http://neurotalk.psychcentral.com/forum118.html

Reflex Sympathetic Dystrophy
http://neurotalk.psychcentral.com/forum21.html

Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray:

Darlene :hug:

Hello RSDMOM
 

Welcome to NT! :hug:
I'm so sorry that you and your daughter are suffering RSD. This nasty condition has taken my 40's away from me. We'll see what my 50's will bring :rolleyes:

So many people here understand what this is all about, so make yourself at home. Darlene has given you some great links. Just holler if you have any questions or need help finding your way around.

I'm particularly interested in how you are doing with your pain pump. I have a SCS and would like to know more about the pumps.

It's great to have you here!

Caring,
Rae
:grouphug: