Welcome Wild,

Is it possible for you to re-open your case? I have read that people have done this.

It would be a great help for us if you would tell us what you have tried to help you? Is your RSD, hot or cold?

Before I was diagnosed with RSD/CRPS I started using a pain therapy I read about on a fibro site-magnesium and malic acid. Please google it.

What has helped me the most is low dose naltrexone, a therapy pioneered by Dr.Bihari and embraced by a CRPS specialist, Dr. Pradeep Chopra, who has several informative CRPS YouTube videos. In addition to this, pool therapy. LDN, if you haven't tried it already may help your fibro, too.

Originally Posted by PurpleFoot721
Here are all of the links that I have that I would send to those who want to learn a little more about CRPS. Some are a little out of date but still useful, ie. Dr. Hooshmand's site, and the last is the video by Dr. Pradeep Chopra that many here have recommended for me which was very well done. Hope this is what you were looking for.
http://www.rsdhope.org/

http://www.ninds.nih.gov/disorders/r..._dystrophy.htm

http://rsds.org/

http://rsdrx.com/index.html

http://rarediseases.org/rare-disease...ophy-syndrome/

http://www.rsdinfo.com/

http://www.thblack.com/links/RSD/

www.youtube.com/watch?v=s3LKhOZ8mAM