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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Old 07-05-2007, 02:22 PM #1
dealingwithtos dealingwithtos is offline
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Default No Cure

Hi Everyone.

I need to get an opinion from all of you...

I've just been told that there isn't anything that they can do for my RSD. It went undiagnosed for 3 years so it has progressed. I've tried a nerve block, but was so absolutely painful that I can't get another one. The doctor that I went to does not give pain medication before the procedure so I'm screaming in pain. The nerve block did nothing for my pain. My eye went droopy like it was supposed to, but no relief in my arm at all.

I'm on medications to help with the symptoms. Neurontin, muscle relaxer, depression medication, etc. I tried physical therapy but turned out to be expensive and hard to be away from work. In February of this year, I had a blood clot in my RSD arm. So, I was on blood thinners for 3 months before the clot took care of itself.

So my doctor told me that there is no cure, no research and no definitive treatment. So, where do I go from here? I've pretty much tried all that I can. It's hard to come to a conclusion that there isn't anything and that all there is to do is cope?

I know many of you are saying "well, duh". I guess I'm having a hard time accepting that there isn't anything that anyone can do. My RSD is a result of my TOS rib resection surgery in August of 04. This wasn't a result of a fall or work injury. So, I have no disability to turn to.

I know that I'm lucky to be working at all, but every day is getting harder and harder. I literally come home and sleep from 7:00-9:30 on my couch and then sleep all night. I'm exhausted and in pain. I bought a new car because I couldn't ride in our explorer as it was too bumpy. I am taking no narcotics because of how they affect me. I wouldn't be able to work full-time if I was to start taking them. I try to do alot of deep breathing and try to stay at stress free as possible.

Haha - stress free? I just found out that I'm going to be a grandmother. I know this should be a wonderful thing, but I'm 36. It's my husbands son who is 20 but has no job, no high school diploma...

How do all of you cope with RSD and the fact that this isn't going to go away?
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Old 07-05-2007, 02:36 PM #2
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Default Hi Dealingwithtos

I got my RSD from a rib resection also.

My opinion is that if this Dr. is the first Dr. that you have went to, I would find another one that will try and help you more. No, you can't get well but you can get to a better place with it with the right help.

I honestly believe that Anesteologist do better at blocks. I just had a friend here to tell me that her PM Dr. didn't put her out or give her anything. That didn't surprise me with her Dr. He's a quack anyway. I recommended her to see my Anestologist. He puts you out enough that you don't know what's going. I had 3 blocks and I am in remission. I also had triggerpoint injections and spent a lot of time in therapy. The therapy wasn't like lifting weights or pulling on therabands. It was massages, heat pads, and myofasial release.

Don't give up and don't just take the word of your first Dr. There are Drs. out there that will aggressively fight the RSD and try to make things better for you.

Ada
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Old 07-05-2007, 02:45 PM #3
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Hi Ada,

To be honest, I'm just tired. I feel like I can just get to work everyday - I don't think I can fight right now.

My IM doctor said that he would give me a referral to go to a doctor down at the Mayo Clinic in Rochester Minnesota. He didn't know if he could help me, but thought I could give it a try. I just don't want to take the time, energy, vacation time to go down there to have them say that they don't know or go through another painful procedure. We haven't decided if I'm going to go down there or not...

I feel that I do my own physical therapy every day by using the arm - as normally as possible. I don't want to pay $20 per visit for what I can do at home. I'm sorry to sound like a cop out, but I just don't have the vacation time to keep screwing around. I feel like I've screwed around with this for 3 years.

I'm sorry to sound so frustrated. Thank you for your comments...
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Old 07-05-2007, 03:01 PM #4
debbiehub debbiehub is offline
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Default Hi

There are 2 treatments I would give somethought to- Low dose ketamine infusion and hyperbaric oxygen...They didnt work for me but I do know of people who have had success....

Debbie
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Old 07-05-2007, 03:29 PM #5
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Default Hi,

I do know what you are feeling. I get that way with my situation. Dr. after Dr. after Dr.

I had my surgery in 2000 so that's when mine came on.

It will take some time to figure out what you want to do and there will be more people come on with good ideals. After you get your second wind maybe you can tackle things like the Mayo Clinic and some other things that will be mentioned here.

I just wanted to let you know that I feel for you and do know what you are going through.

Ada
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Old 07-05-2007, 04:14 PM #6
dealingwithtos dealingwithtos is offline
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Thank you so much Ada.

I'm just a little fed up right now. I think I need to wait awhile before I can handle another "I don't know."

What frustrates me is that I was going to a pain clinic. I found out later that my doctor was a fellow - not the staff doctor. She said that there's nothing else other than pt. So, to hear other avenues I could have tried, frustrates me.

I think it'll do me some good to just leave it alone for awhile and get to work everyday with a smile on my face...
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