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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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copied this from another thread for new member, Jannelle.
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Last edited by Jomar; 03-28-2009 at 01:48 AM. Reason: made new thread |
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"Thanks for this!" says: | Dew58 (03-28-2009) |
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Jannelle,
I have a terrible time with my arms falling asleep at night. It will wake me up as often as the pain alone will. I dont know what to tell you to help with it just know you are not alone with it. For hypersensitivity mine is mostly on the top & I use a cream my pharmacist came up with for me. It doesnt work as deep as it sounds like you need. I put its name in another post. It works so well for that & the burning. I did find if I sleep with my worst arm on an extra pillow in bed it helps but only until I roll over & change positions. I am not good about staying in one position all night. Take care. Hugs, Denny |
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"Thanks for this!" says: | Jennelle (03-31-2009) |
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Thanks so much about the reply on your arms falling asleep at night too!!!! This forum (and computers) are so new to me I don't know if I am doing it all in the right way! I try and sleep on my back only now-so hard! What is the name of the cream, I would like to try it! I can't thank you enough... I have felt so alone lately, even my family doesn't seem to want to understand my condition and I'm a nurse-you think I would know more. I do pediatrics though and never heard of this problem before. Quick question, when I log in to the first nerotalk page how do I find the right search for rsd thread/forums... I tried a search and come up empty. Should I be going to a different link in my favorites? Thanks again!!!!
Jennelle |
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Magnate
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I wanted to say about your arms falling asleep. Mine did that too. I also have TOS so I chalked it up to that. I spent almost 4 years in PT though and they stretched my fingers and arms and massaged them and I no longer have that problem.
I have the deep nerve pain too. I can't squeeze my body anywhere without making myself hurt. I don't know if we can get rid of that part. I haven't. I am doing great with my RSD though. I have been off my meds for months so I do know that it can be done. It does take time though to get to a better place with the RSD. Ada |
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"Thanks for this!" says: | klb1553 (04-01-2009) |
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Thank you for the warm welcome!!!! I have a question for you what is TOS?
Jennelle |
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#6 | ||
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Quote:
I thinks it's great you are off all your meds. My goal has always been to try and manage my RSD with as little medication as possible. I left my job 3 years ago and so far the only medication I have been able to stop is cymbalta. Where is your RSD and how long has it taken to get where you are now? Take care Sherrie |
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