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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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Hi, I'm new to the forum. Found this place during research on the Spinal Cord Stimulation for Permanent ulnar nerve damage.
I have been diagnosed with Ulnar Nerve Damage, Chronic Pain, CRPS, RSD, RSDSA, Caustlgia, Neuropathty by several doctors. The diagnosis is confusing for the CRPS, RSD and RSDSA as when researched they seem to be the same thing, but several of the doctors I've seen say I have all 3 along with the other diagnosis', where as others will assign one sometime 2 of them along with the other diagnosis'. My history of my Ulnar Nerve Damage is a bit long and very rare, so I want to tell the whole story as I have yet to find another person on the planet that has had it happen to them. I appologize if its jumps or is all over the place, my concentration is horrible from the chronic pain and sleep deprivation from the pain. I had went to the doctor originally for a sore elbow, it was painful to bend or extend my arm,, the pain was not bad it was more annoying like a "pulled muscle" and in my forearm. After x-rays showed no fractures or broken bones and no swelling or infection, my family doctor sent me to a sports orthopedic doctor. The doctor diagnosed me with "golfer's elbow" and we joked that it was really "scrapbooker's Elbow", since I don't golf and Scrapbook a whole lot and at the time I was a Scrapbook Teacher at Jo-Ann's for the past several months, that took me 5 yrs working there to finally get ![]() The next day I tried telling myself it was going to get better and went on with my daily routine. But a few hrs into my work day that was beyond unproductive, many of my co-workers kept telling me I looked horrible and should go home and so I did because I just couldn't take the pain. I called the Doctor's office to be seen cause things just weren't normal. Long Story short, the receptionist was a broken record player repeating that at the injection site there would be some pain, redness, swelling and burning and it was normal. Though, I had numerous times that it was my entire arm and hand from my shoulder to my finger tips that was excruciating pain, burning, pins and needles so intense and muscle spasms you could see with your bare eyes. She did put me on hold and talked to the doctor, who knows what she said to him because she just repeated herself and basically they would NOT see me. Feeling like I was going crazy I called my sister, who is a nurse, to see if I should be seen by a doctor or not. She missed my call, but called me after I had gotten off the phone with my husband who told me to go to the ER. My sister said my symptoms by no means were normal and needed to be seen ASAP by a doctor. Not wanting to go to the ER and sit there for hours and not be diagnosed I called my family doctor and he said to come in immediately, I was taken in as soon as I got there. He said that it appears that the needle hit my Ulnar Nerve and its possible i now have nerve damage. He prescribed some more meds and said to take those and call him at the end of the week if not better. I called him the next afternoon and said I can't take the pain anymore its getting worse. He then sent me to a plastic surgeon who also specializes in upper extremities. It took 4 months but was finally having surgery and would know what exactly was going on. The surgeon wouldn't confirm but said it was possible the nerve was damaged by the needle during the cortisone injection and there was some white substance that was on the outside and inside of my nerve that was possibly cortisone but he never sent it out to find out for sure. After surgery, he sent me to PT which didn't really help much and I only had 10 appts since that is what my insurance covered. He refused to write a note saying I needed more for the insurance to cover the overage, which they said is all I needed to get more approved appts. I have seen several different doctors from different "specialties" and none can come to the same procedure to go with. Though 3 Pain Doctors seem to think that the Spinal Cord Stimulator will help even though they all said its success rate for upper extremities are not good. I have had several other doctors and PT specializing in hand and upper extremities, also including a pain doctor tell me that the spinal stimulator won't be helpful. I had tried the TENS machine in PT and it was excruciating and made my symptoms worse. Though, the doctors say its similar its different. I know I can try the stimulator on a 2 week basis to see if it helps or hurts. But since my whole incident with the cortisone shot, I am petrified of needles and my trust in doctors is weakened. I guess I'm just looking for personal testimony from those who have nerve damage in their arm(s) what your experience is good, bad, in different? I find hearing from regular people versus doctors statistics is a better for me to make my decisions cause the one thing i learned is Doctors don't tell you everything and sometimes outright lie, especially when your injury is caused by another Doctor. Thanks for reading and looking forward to hearing your experiences. |
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