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-   -   Spinal Cord Stimulator for PN (https://www.neurotalk.org/peripheral-neuropathy/175571-spinal-cord-stimulator-pn.html)

tailam08 08-29-2012 10:23 AM

Spinal Cord Stimulator for PN
 
I was diagnosed with PN about two years ago. Recently, I found out about the spinal cord stimulator (SCS) were used for to reduce the pain associated with PN with Dr. Morar at Dayton Interventional Radiology. Before having it done, my back pain was about 8/10. Now, it is about 1/10. Has anyone else had the procedure done?

Leesa 08-29-2012 02:44 PM

Many many people have had the SCS implanted. You might post in the spinal disorders forum.

I had the SCS implanted years ago, as I had horrible sciatica & PN. It was hoped that the SCS would help it, as like you my pain was usually at about a 9. :eek: Medications wouldn't even touch the pain. They implanted the device and I had it for 6 months. It didn't seem to help and iin fact seemed to irritate the sciatic nerve even more. It was reprogrammed many times to try to help me, but nothing worked.

Then to make matters worse, the fact that I was thin was a downer cause the " generator" started to work itself OUT of me. The corners of it began to poke thru me! UGH. So they had to take the whole thing out of me, which wasn't fun cause of scar tissue around the generator AND the leads. I still have a painful spot in my mid back due to scar tissue. :rolleyes:

So - I was hopeful, but it was not to be. Darn it. LOL I had hoped for the Morphine Pump, but the fact that it's even bigger than the SCS ruled that out. So I'm just on stronger medications now -- and i found a new GP who worked very hard to find a combo of meds that ACTUALLY WORK! No other doc was willing to work as hard as this GP. Finally after 26 years, I'm "comfortable."

I'm so glad YOUR stimulator has helped you! That's wonderful to hear, and I'm even happier to hear that your pain levels are SO LOW!!! Thank God! You suffered long enough! Take care, and please keep us posted on how you are doing, ok? God bless. Hugs, Lee

tailam08 08-30-2012 01:30 PM

Leesa,
Glad to hear that you are doing better. Just out of curiosity, what brand of SCS did the doc used on you?

Rrae 09-05-2012 01:07 AM

SCS Forum
 
There is a forum exclusive to SCS and Pain Pumps.
Here's the link to take you there:
http://neurotalk.psychcentral.com/fo...ysprune=&f=118

It's listed as a Sub-forum in the Medications/Treatments Forum.

Hope this helps.

Rae
:grouphug:

Leesa 09-08-2012 08:16 AM

Sorry it took so long to reply. I had the MedTronic SCS. Too bad I still don't have it. :(


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