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Real members of MyFibroTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Has Anyone Had The Spinal Cord Stemulater? I Would To Have More Opinions On This It's My Next Step.

A MyFibroTeam Member asked a question 💭
Housotn, TX
September 15, 2016
 · 
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Answer Summary

Members shared mixed experiences with spinal cord stimulators for chronic pain, with some reporting significant relief and others finding... Read more

Members shared mixed experiences with spinal cord stimulators for chronic pain, with some reporting significant relief and others finding limited benefit or complications that led to removal. Several members described practical considerations including the surgical procedure (which involves placing leads under the skin along the spine and a battery pack that requires periodic charging), potential for the device to shift over time requiring adjustments, and varying success rates with some achieving around 75% pain reduction while others saw minimal improvement. A recurring theme was the importance of thorough research, weighing the risks of any spinal procedure against the severity of uncontrolled pain, and recognizing that for many members this represents a last-resort option after exhausting other treatments.

A MyFibroTeam Member

Depending on your diagnosis, not having Spinal Surgery can cause you to be paralyzed. You should take any back or spinal surgery serious. The difference between some having these surgeries and others not having it is that not all of us have a choice.

September 25, 2016
A MyFibroTeam Member

My mom had a spinal cord stimulator put in (yes it does require surgery) however, a year later she had it taken out because it didn't help at much as she though. Also, it was a little but of a hassle because you have to "charge" it every now and then.

September 16, 2016
A MyFibroTeam Member

I'm so glad you are having much more luck than I have. Thank you for sharing your story.

September 15, 2016
A MyFibroTeam Member

Here I go again, I'm not sure when you had yours put in @A MyFibroTeam Member but I just had mine put in 5 week's ago and I tell you, I'm so happy with mine. The healing for me wasn't good, I had to get use to the healing, but so far with the little pain meds I now have to take. I feel like a new person. My inpaint don't move and it last for 10 year's, you may need to look at medtroice ,it's all put right under the skin. And yes it may not be the best thing for some, I think things has got better over the years, as a matter of fact. One of the Dr. Is getting ready to have surgery for one. Mine works all over the body. Feet and all head to toes and you can cut it off when you want to.

September 15, 2016
A MyFibroTeam Member

I understand exercise not being right for you. Sounds like a gentle stimulation is better so as I can tell cranial sacral therapy is a good touch for you because it's mild hands on the base of spine at neck and low back and helps spinal fluid flow.

September 21, 2016

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