kerry
Hello Sharon. I have had rsds for about 7 years diagnosed, 16 total before being diagnosed. There are so many components to this dreadful disease and yes, I too get dizzy and tingling. I also get weird electrical pains in places other than my affected limb. I feel for you, this disease is awful. I just keep on going. I can not receive any disability because I do not have enough work hours in. I work two days a week and it is killing me. The pain is a part of my life and all the other symptoms that go with it. I stopped all the medications: neurontin, zanaflex, sympathetic blocks, blah,blah,blah.... I would like to go back to the blocks, because I need to have surgery on my affected limb, but my insurance company, (COBRA BENEFITS) has no anesthesiologists in my network, that work out of the hospital that I use and am supposed to have surgery at. I feel I am stuck between a rock and a very hard, dark place. I have a will bigger than the world, and all the little weird things that I encounter with my body everyday are just what I feel to be part of rsd, I just try to deal with it as best as I can. I feel so alone.....