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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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#21 | ||
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Sorry, I didn't really state my point in my post - An earlier poster is right, it is what it is and it's going to do what is going to do. There is no magical solution. I'm not saying that is easy to accept that at all - I haven't yet - but it might be good to keep in mind as much as possible. I wish you the best.
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#22 | ||
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"Thanks for this!" says: | maygin (02-23-2015) |
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#23 | ||
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Yes you did explain yourself correctly and it does help . Thank you for sharing your story with me. Even trying to do things outside of your wheelchair is great. Your strength is very inspirational. Don't give up! I hope you have better days. Thanks for helping me with this |
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#24 | ||
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Junior Member
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As far as I know, gabapentin is not addictive in the way that perocet and the other opiods are; however, the body can become used to it, so one cannot just stop taking it without stepping down on it. The biggest side effect is drowsiness, which hit me hard for the first month, but then went away.
There are many other medication options. A drug that works for one of us might not work for you. But pain is a resource hog, so it's important to get it under control, especially if you want to stay in school. While I have no proof of this, I believe that my working 12 hour days 6 days a week leading up the election caused the spread. The pain was super concentrated before that. Of course, stay in school if you can; I just urge you to pace yourself and try not to get super stressed and overwhelmed. It might be a great idea to see a therapist to help with relaxation techniques to get you through the stressful times, like finals. There are things besides medication, like positive thinking, mirror box therapy, desensitization, laughter therapy, yoga, meditation, thai chi, and qi quong that can help with the pain and reduce stress. Try out each and see what works for you. There might even be videos at your school or a free class. For me, most of that didn't work until the pain went from intolerable to tolerable with medication. Mirror box therapy and desensitization were the only things that moved the pain notch a little before we found meds that worked. I wish you the best. You are welcome to PM me if you ever want to talk. I'm so glad my post made you feel less alone. There is power in feeling like you aren't the only one. Take care! ![]() |
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"Thanks for this!" says: | birchlake (03-04-2015) |
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#25 | |||
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I'm so sorry to hear of your continued problems. Totally, totally agree with you on this. 2 years back, I could "feel" the thing spreading, and I had been burning it hard on both ends, with rehab efforts and projects for work. After one particularly stressful 12 hour day I ended up in the ER, and they all scratched their heads the same way. Quote:
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"Thanks for this!" says: | maygin (03-09-2015) |
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