Looking to give and get information about RSD and treatments as well as spinal cord stimulator treatment. I have been dealing with RSD for six years now. I have just gone through a procedure for a temporary spinal cord stimulator. I would like to find others who are going through what I am going through to possibly discuss and learn from each other.

Hi, I have rsd in my leg and have had as many different treatments/procedures that you can name. About a year ago they put in an ANS spinal cord stimulator. I would love to chat with you and talk about this. If you want you can email me at shoff1@gte.net

We almost sound like twins. I've had RSD now for 7 years, which originally started in the left leg (knee area). It is now also in both arms, shoulders, and neck, and possibly also involves the left side of my face. Also, I'm on day 4 of an SCS trial. If you'd like to talk you can e-mail me at gladysf@worldnet.att.net.

Take care.

I was diagnosed with rsd in 8/00, and my doctor is suggesting a nerve stimulator trial.I'm curious as to why you waited so long before trying this option.

I was diagnosed a little over one year ago with RSD. It is in my left arm and left shoulder. Unfortunitly I am also left handed. I have had many blocks, pt, and assorted meds. I am in need of knowledge about rsd. I am now having alot of back pain. I have been told all they can do is give me meds and do periodic blocks.
Please email me at chsmithville@AOL.com

Thanks
Beverly