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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 |
11-23-2014, 02:26 PM | #33 | ||
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New Member
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I have been diagnosed with CRPS. I'm on very high amounts of opioids (Fentynal patches). I've been on high, high opioids for 2 years and my Doctors are pushing me to get a SCS. They claim that taking these high doses of pain meds isn't sustainable. Does anyone here have a successful SCS story with RSD or CRPS ?
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