Quote:
Originally Posted by rtmcmahon631
hi my name is bob and i haven`t posted any thing in a long time.I was injured in 12/18/2007 by a fall at work on ice. I went to the docs and was told i have tennis elbow torn ligament in my arm opt to a cortizone shot than a operation just to finnish out my work season.By this time because its workmens comp it was april.after receiving the shot it worked great until sept. I then received another shot and my world went upside down it was the most painful thing I almost past out. the next few days it became very swollen and it turned red i then called my docter and he said it looked like i had rsd.I then went to a pain doc which put me on all sorts of medsFor thenext few months he decided to try i block in my neck which sent my rsd even more out of control. Then he said that a spinal stimulator was the next step.Not liking this i went for a second opion which was with another pain doc in a large clinic.He then put me on differnt meds which has helped my pain isn`t as bad but still there i now have color changes but not as often and my pain comes and goes which is alot better.they tried beir blocks i think it was 5 of them It was great for about 2 weeks then back to where it was before.Now it was suggested that I have a spine stimulater again.I said i would try it the comp isurence approved it then denyed it and sent me to a surgen a M.E. he said that i should take the risk of the rsd and get the arm fixed which is scaring the heck out of me. the first pain doc said that i should never let anyone to operate on it.Dont know what to do.Dont know if anyone went through this
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Hello Bob....
I am sorry for your situation with your RSD.. This is a terrible condition, very confusing and finding proper, timely health care is a must...
I understand your Dr. trying the pain meds and blocks as RSD can be caused by the smallest of injuries and treatment is a must, quickly if remission is even possible... But I question the spinal cord stimulator as a quick resolution and even question more about doing surgery..We are considered a "no touch" patient and intervention like that can cause spread of our RSD... I believe the idea of surgery would not be the best option..rather a third Dr. to give you a bit more insight on your case..possibly an anesteslogist, neurologists or another pain management Dr... our options are so limited at best but at the same time we need to explore everyone of them to maximize our care..and WC does not make things any easier..My suggestion is to get more medical knowledge, input into your care then make your selection on how to proceed...
Let us know if we can help you in anyway... I am sorry you too have to live in such pain as we all do here with our nasty friend, RSD!
Best wishes, Kathy