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 05-01-2007, 08:14 PM #11
Imahotep Imahotep is offline
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Imahotep Imahotep is offline
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I have a very small amplitude high frequency tremor when I try to go to sleep. Usually I can barely feel this tremor but somehow it prevents sleep. An anticonvulsant (tizanisine) almost completly takes care of it. There are several other symptoms that can interfere with sleep. Usually the pain shuts down as I start to drift off but some drugs and/ or circumstances will cause the pain to get worse and prevent sleep.

The drs have done an excellent job of getting drugs which enable me to sleep. Sometimes I still have trouble.
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Old 05-03-2007, 04:24 AM #12
miss irie miss irie is offline
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miss irie miss irie is offline
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Hi.

Having trouble sleeping is a problem I've been dealing with for quite some time. At one point I did try some sleeping pills but this really isn't a long-term solution. Recently I've started taking gravol at bedtime and this is helping me to fall asleep. Just thought it might be an option for others who also suffer from sleep difficulties.

Wishing everyone well,
Miss Irie
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Old 05-03-2007, 01:57 PM #13
Kwaker Kwaker is offline
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Quote:
Originally Posted by mrsmac View Post
Feeling kinda silly posting a message but I so need to talk! Feeling as though I am losing my mind!

I will try to keep it short hopefully you will respond.

Had tarsal tunnel release end of Feb. 07. The next morning, extreme burning from foot to upper calf. Worse pain I have ever been in. Drs. order to keep splint and wrap on for 15 days. I had to remove at day 3, to painful. Noticed then the purple color. At 3 week, Dr. said had mild crps. I had never heard of it, and i am ashamed to say i am a nurse. Long story short, now 2 month later. Pain is better, the burner is on simmer. Ankle still swollen, ruddy in color when sitting or standing, normal color when walking. It feel like it is wet at times, but dry when I look. Extremely sensitive, i wear a sock and that helps. The reason i started surfing internet today is to find out if the reason i can not sleep is due to possible crps too? i guess if this is truly crps, it is...right? My case (if it is crps) is mild compared to other i have read about. i pray it stays that way. Any comments? Needing a friend who understands.
Hi, I'm new here, too.
Not new to RSD, though as I've been dealing with it since '93.
Sleep is a part of it in my case and lots others. Generally, my sleep is a couple hours a night for weeks then maybe a 6 hour stint of sleep every now and again.
It sucks, but on an up side (tongue in cheek) there's lots of time for late night tv viewing of reruns and infomercials and late night internet surfing with no interuptions!
Melatonin does help now and again to push that sleep closer and earlier in the am, but check with your doc first, to be safe, though i've had no bad side effects or interactions.
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