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 03-30-2012, 07:22 AM #2
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catra121 catra121 is offline
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Join Date: Jan 2010
Location: Illinois
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catra121 catra121 is offline
Senior Member
catra121's Avatar
 
Join Date: Jan 2010
Location: Illinois
Posts: 1,785
15 yr Member
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Welcome...and I am very sorry to hear all that you are going through. I hope that you are able to get some answers at the clinic in a few weeks...but RSD is often very misunderstood by doctors and medical professionals. Many people go years without a firm diagnosis and even once we have one there always seem to be doctors out there who want to tell us we DON'T have it (the same ones who say it doesn't spread or can't be anywhere other than a hand or foot...yeah...they are out there with their wacky theories).

I understand your feelings about the meds...I personally have gone off most of mine that were for the pain because I was concerned about the long term affects they would have on me. But we all need to do what is right for us as individuals and what allows us to get the best quality of life.

For me...the single biggest thing that has helped my RSD up to this point has been the physical therapy. It's very hard to do and hurts like all get out...but it has given me my life back. I was stuck in a wheelchair and couldn't do hardly anything for myself...now I am able to be on my feel all day long (still need to use a walker) and can go out as much as I please. The pain is still there...but the function is back and I will take it.

Another thing which I just started a month ago is tDCS. This has been one of the first things in a long time that is actually helping with the PAIN and the allydonia. It is pretty inexpensive as far as treatments go...the equipment only cost me $300 or so and I do the treatments at home by myself. There is a thread on here about it and I highly recommend reading through it. I don't know if you have RSD or not...but if you do I would make this one of my first treatment options. It is not invasive and has little to no side effects so it's definitely worth a shot given the number of people who have found relief with it. Also...at $300...it is much much cheaper than just about any other procedure you could find out there. Not to mention the savings on prescriptions if you are able to come off of some of those meds, right?

Good luck to you...I hope that you find some answers and some relief soon. This really is a great site to find support and understanding from people who know what it is like to go through what you are dealing with. Good luck.
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