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 02-11-2014, 03:07 AM #1
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Default What an excellent idea

I suffer from chronic pain and have done since a young child and I don't have CRPS. My heart bleeds for all that you go through.

Pain is gruelling and all consuming. To have a forum that is threaded with thoughts and activities that will help pain sufferers, well, it's just exciting to believe everyone from across the globe can pull together for one another.

I read an article from a thread posted by zookester this morning and it refers to activities young sports people have participated in with the aim of further gaining relief. I cried reading that article. I was a junior state champion athlete but I don't think my pain levels ever reached (in those days) a place where I would willingly stick my hand into a dry substance of raw barley, rice and fine sand and rotate it through for 20 minutes or more to stimulate the nerves. The author noted some cried and some even vomited. No doubt the same thought process that is applied with exfoliating burnt skin. I still feel ill to think that in our lifetime we have willingly submitted ourselves to such purposes in an aim to find relief.
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Old 02-11-2014, 07:44 AM #2
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There are indeed websites that track what works for different people that include non-medical treatments. One of them is called curetogether.com and if you log in there, and type in complex regional pain you'll see a few people have added what works and what doesn't for them (under "Treatments").

If more people used that site, then I'd think you'd get more useful information out of it. No need to reinvent the wheel... I think patientslikeme.com does this too, but not for CRPS.

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Old 02-14-2014, 10:27 AM #3
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Quote:
Originally Posted by DocJohn View Post
There are indeed websites that track what works for different people that include non-medical treatments. One of them is called curetogether.com and if you log in there, and type in complex regional pain you'll see a few people have added what works and what doesn't for them (under "Treatments").

If more people used that site, then I'd think you'd get more useful information out of it. No need to reinvent the wheel... I think patientslikeme.com does this too, but not for CRPS.

Best,
DocJohn
Thanks Doc!

I had a chance to look at those sites and while they were interesting, they were nothing at all like the detailed, subjective reporting, community driven research I'm proposing. I always find it helpful to look at what others have done to help me clarify my vision and so muchas gracias.
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