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SCS & Pain Pumps For spinal cord stimulator (SCS) and pain pump discussions. |
View Poll Results: Do you have a SCS or Pain pump? | ||||||
SCS? | 121 | 85.21% | ||||
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Pain pump? | 13 | 9.15% | ||||
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Worked well for me | 38 | 26.76% | ||||
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Works somewhat / partially | 44 | 30.99% | ||||
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Didn't work for me | 9 | 6.34% | ||||
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Had to have it removed | 13 | 9.15% | ||||
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Had medical complications | 15 | 10.56% | ||||
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Had mechanical malfunctions | 10 | 7.04% | ||||
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Still in but turned off | 17 | 11.97% | ||||
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Other issues explain in a post please. | 20 | 14.08% | ||||
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Multiple Choice Poll. Voters: 142. You may not vote on this poll |
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Thread Tools | Display Modes |
06-14-2012, 07:03 PM | #13 | ||
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Junior Member
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Hope Im in the right place .....Hi guys, I had SCS surgery in December 11.my CRPS is in my left foot.I am still having severe pain around the surgery sites.Cant do much of anything.Still on crutches and in wheelchair.I would love to hear of fellow scs implant people.Im in UK and had my scs surgery at The Walton Centre .my neuro nurse check up is in August...any advice etc
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