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 05-29-2010, 01:13 PM #1
fraher fraher is offline
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fraher fraher is offline
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Join Date: Mar 2009
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Default ganglion/crps

hello,has anyone had a ganglion on there hand and crps, if so how has it been grateful for any info,i have had crps for 5 years ,just diagnosed with the ganglion.many thanks, olga
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Old 05-31-2010, 09:58 PM #2
loretta loretta is offline
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loretta loretta is offline
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Originally Posted by fraher View Post
hello,has anyone had a ganglion on there hand and crps, if so how has it been grateful for any info,i have had crps for 5 years ,just diagnosed with the ganglion.many thanks, olga
Hi Olga and welcome to Neurotalk. I'm sorry you haven't received any responses yet. It must be unusual. I've had RSD 15 years-full body now and internal. I haven't had what you asked about. Just make sure you do the research especially if they want to operate. I got RSD after surgery. There are procedures to prevent spread if surgery is absolutely necessary.
This is a wonderful compassionate group of friends. Very supportive and educated. RSDSA is a site that provides a lot of good information. Also rsdrx.com puzzles list is wonderful. It has 146 questions or (puzzles) with the Drs. answers. Dr. Hooshmand practed RSD for 40 years in Florida. He is retired, but his website is excellent.
At the beginning of Neurotalk you might do a 'search' of RSD and Ganglion.
Take care and please let us know how you are doing. One of your new friends, loretta with big hugs
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Old 06-01-2010, 04:34 PM #3
fraher fraher is offline
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fraher fraher is offline
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Originally Posted by loretta View Post
Hi Olga and welcome to Neurotalk. I'm sorry you haven't received any responses yet. It must be unusual. I've had RSD 15 years-full body now and internal. I haven't had what you asked about. Just make sure you do the research especially if they want to operate. I got RSD after surgery. There are procedures to prevent spread if surgery is absolutely necessary.
This is a wonderful compassionate group of friends. Very supportive and educated. RSDSA is a site that provides a lot of good information. Also rsdrx.com puzzles list is wonderful. It has 146 questions or (puzzles) with the Drs. answers. Dr. Hooshmand practed RSD for 40 years in Florida. He is retired, but his website is excellent.
At the beginning of Neurotalk you might do a 'search' of RSD and Ganglion.
Take care and please let us know how you are doing. One of your new friends, loretta with big hugs
thank you for the information, i will have a search.i have rsd in my right hand which is where the ganglion is,also my hips and legs,i have been regularly coming to neurotalk for information,it is a fantastic site,again thank you loretta xx
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