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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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Junior Member
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I have RSD, I am in soo much pain right now, on some websites they say not to use ice on the affected limb, is that true?
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#2 | ||
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Junior Member
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People argue about the ice thing. I never use ice because my leg is generally so cold as it is. We did use ice on my leg during PT before knowing I had CRPS.
Are you seeing a pain management doctor? They should be giving you an idea of what steps to follow next. What meds have you tried? I was 17 when diagnosed so I know how devestating this is during your teen years. I felt like my world was crumbling. Please PM me if you ever feel like chatting about that. (I'm 25 now.) |
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"Thanks for this!" says: | ginnie (10-23-2012) |
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#3 | ||
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Guest
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No Ice No Hot and cold water contrast therapy.
see picture |
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#4 | ||
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Member
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#5 | ||
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Junior Member
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Yes I am seeing a pain management doctor but not as often as I should due to bills that we can't afford. They have me on tylenol and ultram or vicodin for pain, flexeril for my muscles and voltaron for swelling. *(I know those might now be spelled correct). What really just made everything worse is that the mri showed bruised bone as well, so they want to cast me or i have to be on crutches at all times. I go to college half day and my high school he other half. I don't know how I will manage that.
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#6 | ||
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Member
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The only thing i think alot of us do is just try and manage the pain. Unfortantly there is no cure and there is no real treatments for it. Im in my young 20s and its crap, its in both my arms, chest and neck. Im looking into diffrent things that MAYBE i could try. But for the last 4 1/2 yrs its just been a matter of managing my pain the best we can.
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#7 | ||
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Junior Member
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Quote:
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#8 | ||
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Member
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Quote:
Hope you feel "better" soon ![]() |
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