← Return to CRPS - anyone suffering with complex regional pain syndrome

Discussion
Comment receiving replies
@daveandchris

It is necessary for me to speak instead of type. I am unable to type very well due to the pain.
10 years ago after a surgery on my right elbow, my right hand developed CRPS. A pain clinic near me was recommended. After the first attempt with a ganglion block, the doctor declared I did not have CRPS and walked out of the room.
In the meantime, I was doing a lot of reading and research. This is when I discovered the Mayo Clinic website. The information it gave was more helpful. But I could not afford to relocate to the clinic. That is when I reached out to a university medical center about a half hour from my house.
Ganglion blocks did not help, but the physical therapist located at the Pain clinic was very good. She understood the need for continued mobility. but she also understood the necessity of not making it worse. For the next year, I followed a daily regimen. I also began to wear compression gloves that seemed to help with the pain and especially kept other things from touching my hand.
I’m a pianist. I no longer play. After about a year, the symptoms began to subside, and one day I no longer had to wear my compression glove. Little by little I was able to live without pain. I was in remission. Unfortunately, my range of motion was compromised enough that I still could not play. My hand was stiff. But the pain, the constant pain, was gone.
Two months ago, I fell very hard and broke my left wrist. Almost immediately I was certain that CRPS would return. Because it involves a broken wrist instead of no injury to the hand like my right hand, it has been much more painful and physical therapy much more difficult. I feel like I still have a broken wrist. A nearby physical therapist made it much worse. I am now trying to return to the university medical center of ten years ago.
A back surgery over two years ago has also left me in pain. I’ve wondered if it, too, is CRPS. I’ve been back to the surgeon, then on to two other clinics. None believe it is CRPS. One said it is my SI joint. Perhaps. I’ve been to so many doctors that I gave up and just try to remain mobile. Walking and not much sitting. Lying down when I just get tired of it. Now, my left wrist and hand.
I cannot take Gabapentin. I’ve taken ibuprofen and Tylenol. I’ve been on a depression med for many years. Also meds for epilepsy and osteoporosis.

Jump to this post


Replies to "It is necessary for me to speak instead of type. I am unable to type very..."

My dear sister,

I watch you with love and belief in you. You have suffered much pain due to everything you mention in your message here. You continue to search for answers and are trying everyday to do your best. Of course, I wish I could take all of your pain away. I may not be able to do that, but I can pray for your healing, pray for your strength and pray for answers. I can love you and believe in you and tell you that I know you are doing all you can. I am proud of you. You are an inspiration to me to keep going on my very hardest of days. In spite of all you endure, you continue to serve others, make efforts to be with friends and family, and carry on with daily tasks. Many would sit down and give up; but not you. Keep fighting, Christie. Never stop moving forward, even if it is inches at a time. In never giving up, we can find ourselves in better situations and find hope and happiness and even joy. I love you so much!! Your sister, Virginia

@daveandchris, giving up piano as a pianist must be hard to reconcile with. You mentioned your pain has got better in your hands but the stiffness remained. Is that something you hope to improve over time to be able to play again, or is that not a realistic outcome? Have you found any other hobbies to help distract from the pain?

I'd like to invite @airey2 who also broke their wrist recently and talked about CRPS issues as a result.

@daveandchris, you mention you have seen many doctors and have given up trying to find one who will listen or offer help. Did you explore your SI joint as one had mentioned?