Reflex Sympathetic Dystrophy (RSD)

[livingwith]

1997 was injured at work. 2000 I had to have surgery on my right arm, medial epicondilis ulnar nerve transplant. Took 6 months before I returned to work, unfortunately my employer would not follow any restrictions that I was on. Went to doctors, specialist, and no one could help me, all they did is put me on different medications that wasted me.
Finally 2009 after another test with a different doctor diagnosis that I had type II rsd/cprs. So they started me at the pain clinic, I have ketamine ...Read the full article

[deanna07]

Wow 12yrs. I have been only dealing with it for 1yr and 8mo and I want to scream. I cant work either. I worked for almost 6yrs in the dementia unit as a nurse aid taking care of others. Are you able to get SS? Mine started after a car accident in my ankle/foot area and has spread upwards all the way to my back. It is so frustrating and depressing. Every ones stories on here make my heart break. I know how it is to feel so lonely and depressed from this. I am hoping once the law suit is done if it ever is that I want to get the ketamine treatment as well. I truly wish they would make it more accessable for us.