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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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My doctor is giving me a choice of either the spinal cord sitimulator or a pain pump. Any one have any advice on both and experiences with them?
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#2 | |||
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Member
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Honestly, I think your too young to have to go with either. If I remember correctly, you said you are 18. You are still young and have a great chance of putting this back into remission. I don't know how badly the CRPS is affecting your life, but unless you have expended all other options I would stay away from both. This is just my opinion. I was offered to go with the SCS but went to another doctor to search for more options before going with it. I would ask to see what other options are available for you at your state of dealing with CRPS.
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. Alaina |
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#3 | ||
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New Member
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Quote:
![]() It was a struggle let me tell you, but I actually went into remission; however, that only lasted a few years. It was so worth it though...to have a few good years without the excruciating pain. I have been on pain medication and ongoing physical therapy, but my condition has not improved. I would recommend trying the pain pump first. You may get the relief you hope for, even if it only lasts a few years... |
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"Thanks for this!" says: | PurpleFoot721 (10-29-2015) |
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#4 | |||
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Junior Member
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I am most likely going with the pump. Nothing else is working. I may be 18, but my CRPS is not going into remission . its been over a year and half since this flare up started. And it just keeps getting worse every day. I have full body and internal CRPS. I have been stuck in the hospital for about a week now because I can't not move anymore. I'm hoping something helps....I want my life back.....
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"Thanks for this!" says: | PurpleFoot721 (11-02-2015) |
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