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SCS & Pain Pumps For spinal cord stimulator (SCS) and pain pump discussions.


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Do you have a SCS or Pain pump?

View Poll Results: Do you have a SCS or Pain pump?
SCS? 121 85.21%
SCS?
121 85.21%
Pain pump? 13 9.15%
Pain pump?
13 9.15%
Worked well for me 38 26.76%
Worked well for me
38 26.76%
Works somewhat / partially 44 30.99%
Works somewhat / partially
44 30.99%
Didn't work for me 9 6.34%
Didn't work for me
9 6.34%
Had to have it removed 13 9.15%
Had to have it removed
13 9.15%
Had medical complications 15 10.56%
Had medical complications
15 10.56%
Had mechanical malfunctions 10 7.04%
Had mechanical malfunctions
10 7.04%
Still in but turned off 17 11.97%
Still in but turned off
17 11.97%
Other issues explain in a post please. 20 14.08%
Other issues explain in a post please.
20 14.08%
Multiple Choice Poll. Voters: 142. You may not vote on this poll

 
 
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Old 07-25-2017, 09:51 PM #39
Sadie77 Sadie77 is offline
Newly Joined
  
Join Date: Jul 2017
Posts: 1
5 yr Member
Sadie77 Sadie77 is offline
Newly Joined
 
Join Date: Jul 2017
Posts: 1
5 yr Member
Default SCS problem
I had my permanent SCS implanted about 3 months ago for a pelvic nerve entrapment. Although it works for pain it is causing some sort of interference with my body. From the start I've noticed a decrease in urine output and large amount of abdominal edema when the stim is on. This is my third time turning off my stim, each time having the reversal of symptoms. I've been off for 1.5 weeks now and have resumed normal urination and bloat is down. Has anyone else had this problem? My Dr has not done a SCS implant for this nerve before and doesn't know why my SCS is doing this.
Thank you for any help
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