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 09-12-2008, 06:48 PM #1
Summertime Summertime is offline
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Default Capapres aka clonidine transdermal

Hello

Anyone have experience with clonidine transdermal?
If so did it help?
How was it prescribed for you?
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Old 12-11-2008, 04:24 PM #2
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Red face Clonidine: "My miracle patch"

Hi Summertime,
I have been suffering from RSD for 8 years. I have been doctoring on and off until about 2 years ago. I was tired of hearing there is nothing I can do for you. I am very sensitive to medications therefore the specialists didn't want to bother with me. I was recently in an auto accident where a young kid hit my family and I head on. I was driving and don't know what I did with my hand with RSD, but the pain had gotten worse, which I didn't know was possible, then before. Finally, a new pain specialist came into my area and my family physician referred me to him. To my surprise, he worked with a well reknowned hand specialist from Philadelphia that I was doctoring with years ago. Anyway, he was talking to be about the ketamine coma and other options for me, but when I went back for my follow-up, he wanted to try the clonidine patch first. I am happy to say that my pain has subsided. This is the first time I have this much relief. I am not saying the pain is gone, but the worst of it is. The only problem I had was keeping the patch on. I need to put in on my thumb and my wrist. It does not stay on. I now have benzoin to put on before I use this derma-bandage to hold it on. The patch is not the best thing for me, esp working with kindergarten kids. They are kind of scared of the bandage, but it is working. I still have the burning and the sensation that someone is squeezing the gutts out of my hand, but the worst of the pain is better. I hope this helps you.
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Summertime (12-13-2008)
Old 12-12-2008, 11:36 AM #3
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Default

Hi hun, Reed had the clonidine patch for a couple of days, but it caused his blood pressure to drop really bad so he was take off it. The short time he had it, it was hard to tell if it helped with pain because he was so drowsy from the low BP. his doc prescribed it one patch on his rsd foot, for 3 days ( I think) then add another. We didn't get that far. It works well from some people, just not Reed.
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Old 12-12-2008, 01:52 PM #4
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Quote:
Originally Posted by Rita View Post
Hi hun, Reed had the clonidine patch for a couple of days, but it caused his blood pressure to drop really bad so he was take off it. The short time he had it, it was hard to tell if it helped with pain because he was so drowsy from the low BP. his doc prescribed it one patch on his rsd foot, for 3 days ( I think) then add another. We didn't get that far. It works well from some people, just not Reed.

Hey Rita, I didn't give that a thought when I wrote about the patch. So far, I have not had a problem with my BP, but I do know that the Doctor said I need to watch it. Ya know, it never fails, though, something that works always seems to have something else that prevents us from taking it. I know that every time I had a bit of relief from some kind of med or something, there was an adverse reaction that stopped me from taking it. I hope that this patch works and don't mess up my BP. I have really good blood pressure, like 100 over 60. Hopefully mine won't drop cuz it isn't high or enough to drop too much. Sorry about Reed, wish it would have worked.
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