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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 |
05-17-2015, 04:15 PM | #35 | ||
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Newly Joined
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Hello, I am posting in hopes that my husband and I can get more testimonials regarding the spinal cord stimulator. My husband has been on the trial for almost a week (coming off on Tuesday) and so far he seems to like the effect it has on him. I am just somewhat worried about having the implanted SPS permanently. I want to think positive but also want to know the reality of it once the procedure is completed. Are there people out there who can truly say that the SPS has really worked for them? Please help us on making our decision easier. Thank you .
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