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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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Hi again! I just started at a gym this week, like I said I was going to in my last post. =) I am a woman of my word!
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"Thanks for this!" says: | AintSoBad (12-14-2009) |
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In Remembrance
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I think it's Wonderful that you're actually doing it! Not just talking about it! I'd say, Yes, this is normal with rsd. My first suggestion is, that you start slowly. Start with warm ups and stretching. Maybe for a month or so, until it doesn't hurt so much. It's really important. 'Exercise in the rsd world, doesn't usually mean 'strengthening', that's gonna hurt! ( do you have TOS or anything besides the rsd?) Does your gym have a warm pool, that you can get in and 'resistance' walk? I'd guess that would be your first real exercise. Many people here rave about it. Then, before you shower and leave, perhaps a short stay in the hot jacuzzi? I'd be afraid of those bands, especially to begin with... Very happy for you! ![]() Thanks! pete |
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"Thanks for this!" says: | suz66 (12-12-2009) |
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#3 | ||
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#4 | ||
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Hi Suz -
Can you get a good physical therapist's opinion? One that knows about RSD? Maybe your doc can give a script... The best of luck to you. XOXO Sandy |
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"Thanks for this!" says: | suz66 (12-14-2009) |
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#5 | ||
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Speaking of physical exercise, or rather the absence of, is something I talk about, a lot, with the pain psychologist I've started seeing. I don't know what your situation is, and if you're good enough to be able to even go to a gym, that's good, but in my case, ANY kind of physical exertion is the worst thing for me. I lifted weights at Gold's Gym every day for fifteen years, and now I can't walk up a flight of steps. Really depressing. Anyway, I would just urge that if there is any pain, go slow. Good luck. |
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#6 | ||
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Prior to RSD I got in the gym twice sometimes three times a week. Walked the stairs to my office not the elevator. That changed as my RSD changed. I have it full body and no longer work.
I do however, go to the YMCA 2 sometimes 3 times a week. I water walk, take an arthritis class and cardio splash. I tried water aerobics and my heart rate wouldn't go back down. A side effect for me from my RSD is an increased heart rate even at rest. We are weightless in the water so there is no pain during or after exercise. My pain doctor wrote a script for water therapy. I learned the things I should be doing to help with strength and endurance. Then I tried the different water exercise classes until I found what I liked. I have been going for the last 3 years. Before we developed RSD exercise was important. Now that our activity level has decreased it's even more important that we find what works for us. Take care, Sherrie |
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#7 | ||
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Ahhh Jacciizzziiii. Please pay f9r this.................
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"Thanks for this!" says: | suz66 (12-14-2009) |
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#8 | ||
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Do as much as you feel safe doing and build up more gradually. My soreness will go away a little faster if I exercise the sore muscles very lightly. |
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"Thanks for this!" says: | loretta (12-21-2009) |
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#9 | ||
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Greetings! I have RSD in my Rt arm and hand and was told that it had not moved to my legs, but that I have degenerative disc disease. I used to walk, do aerobics, step aerobics, etc before RSd. I didn't do that much and it felt like I had taken a grater to my thigh muscles. I went again hoping to stretch, but I still had trouble walking . I sat for several hours after I got home with hot packs on my thighs......it actually helped!! I couldn't believe it.....relieved, though.
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