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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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#1 | |||
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Junior Member
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Hello! As the title states, I'm new to this forum and new to RSD. I broke my lefy scaphoid bone (wrist bone) in half in October 2006. Three weeks later I had surgery to fix it. I was in a cast for about six weeks after surgery then started PT where they treated me with heat and ice, along with exercises. The pain and swelling were horrible, and the PT was concerned...even suggested that I could have RSD. Finally, after feeling my doctor was not being truthful with me, I went to a hand specialist in March. To make a long story a little shorter, the first doc had put the screw in at the wrong angle and it was stabbing through the bone and grinding into another bone. I finaaly had surgery June 22 to remove the screw, which miraculously he was able to remove without removing the bone. My wrist had been immobilized from March 6 to July 6...plus the two months before and after the original surgery that messed everything up. The screw did a lot of damage.
I started hand rehabilitation therapy last week, and the PT told me I have RSD. I think my doc may have mentioned it, too, the day the bandages came off. They used ice on my wrist at the end of therapy last Wednesday, and the swelling and stiffness have been really bad ever since...no matter how much I do the exercises and stretches. My family doc told me a little over a year ago that I have fibromyalgia. Anyone know anything about a link or issue with the two diseases? Well, that's my story so far. I look forward to chatting with everyone.
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In Christ, Phyllis . My hope is built on nothing less than Jesus' blood and righteousness! |
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#2 | ||
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Member
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Hi Dreampoet,
Welcome. This is a great place. I know that you will find many friends here. Iam sorry that you have RSD but everyone here understands and are willing to help. This site has saved me. Sue K. |
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#3 | |||
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Member
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![]() First, I want to say Never let anyone ever put Ice on you again... ICE ON RSD IS A BIG NO...It will make it much worse... Also you need to find yourself a Good Pain Management Doc that treats RSD on a regular basis now.. You need to get started on a series of Stellate Ganglion Blocks to try and place this in remission.. I am sorry to hear that you have gone thru such horrendous care with your wrist... That is awful. You have certainly come to the right place for support and understanding. I have recently been diagnosed with RSD and found this forum to be full of wonderful people that are full of information and support. There are many sites that are full of great information that you may find helpful. The useful links site from the top of this page is full of information http://neurotalk.psychcentral.com/showthread.php?t=247 www.rsds.org www.rsdhope.org www.rsdrx.com www.rsdinfo.com These are just a few that can get you started. There is a wealth of information for you to read up on... Also there is a Fibro Forum here http://neurotalk.psychcentral.com/forumdisplay.php?f=12 They have some useful sites listed in the top left of the page. I wish you the best... ![]() ![]() Dawn
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Live Well, Love Much, Laugh Often . |
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#4 | ||
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Member
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hi phyllis,
welcome to the forum. use the search space to see lots of good info on the topic of your choice. there is a bunch of info there. yes, ice is a swear word to rsd-ers unless it is in your drink! sounds like you have had quite a time of it. i hope you find a good doctor. my advice is always do your own reseach and choose your own course of care and meds. no one knows more about you that you do. every case of rsd i have read of, and that is many, is different and people choose different paths. so read read read and ask away if you have questions. joan
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Courage ... doesn't always roar, sometimes courage is the quiet voice at the end of the day saying, "I will try again tomorrow." |
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#5 | |||
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Magnate
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Welcome to the group.
You will learn so much if you stay here with us. I have both Fibro and RSD and several on here do. I was diagnosed with both about the same time. As they said you need to find you a good PM Dr. for the RSD. I would also find a good Rheumetologist for the Fibro. Some PM's can deal with both but Rheume's seem to know a lot about the Fibro. As soon as you find a good Dr. Ask about blocks to help try and put it into remission. For some it works and others it doesn't but I swear by the blocks. I've seen a lot of good success with them. It's too bad that you were put through so much to fix your wrist. I've had many surgeries and have been blessed with good luck in the results but I see so many who don't. There mayb be someone here in your area also that might be able to give you the name and no. of a good Dr. If you could give the name of a big city you are near there might be someone here that is in that area to lead you in the right direction of a good Dr. I hope you do hang around. You will enjoy the company because we all have so much in common. More so then people living around us. Ada |
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#6 | |||
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Junior Member
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Thanks everyone for your welcoming spirit. I tend to "just deal" with pain...thank God He gave me a high pain tolerance. I've read so much the last few days about RSD, and I don't have it anywhere near as bad as so many. I didn't even know what it was until last Wednesday when I came home and looked it up online. I know God will give me the strength to deal with whatever path He has set before me...I know He's still in control. Thanks again for welcoming me and for the advice.
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In Christ, Phyllis . My hope is built on nothing less than Jesus' blood and righteousness! |
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