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Anyone had Spinal stimulator removed? Replaced?

Spine Health | Last Active: Jan 8 7:15pm | Replies (42)

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@glaciermom

Last January I had surgery to reconstruct my spine. I had had two fusions done locally which gave me a few years relief. The L1-2 disc was the only lumbar not fused and spring of 2021 I started having a lot of pain. It took six months of complaining to my pain doctor before she sent me for am MRI. Turned out that the L1-2 disc had ruptured and since the ones below were fused it had collapsed and my spine became "S" shaped. I was diagnosed with adult onset scoliosis.
I woke up one morning and could not move because of the extreme pain. Thankfully I had a medical button and was able to get help. The ER doc was awesome! He talked to me to get an idea of what the problem was then, he went and looked over my tests and notes. When he came back, he kind of was trying to come up with a description of my back. I asked if he was trying to tell me my back was a mess. He laughed and said yes that was it. He had spoken to the neurosurgeons office and was told that they would not touch me. They made an appointment for me to meet with the PA in their office. He told me I needed to go out of state to see a doctor who could help me. Since he taught over there, he knew of the doctors and gave me the name of a surgeon.
I went fully intending to turn any surgery down, I had had enough. But meeting with him and listening to how much success he had had with his spine reconstruction I decided to trust him and agreed to the surgery.
The surgery was nine hours long and the pain was worse than my other fusions. I am fused from T9 to S1. I am a year and a half post surgery and still pain free after having dealt with it for 33 years! The surgical pain is a faint memory now and I am still glad I had that surgery.
I would recommend that anyone considering surgery get information about the surgeon and be sure he/she has a good record doing the surgery.
The medical center where I was referred is part of a university so it is on top of anything new.
I do still have my spinal cord stimulator due to nerve damage years ago. I couldn't live without it. I know because when a doctor was replacing my stimulator he accidentally pulled the leads out. Went 10 days before he had everything he needed and put in new ones. That time I was on Lortab 10's and still had bad pain. As soon as he got me put back together the pain was controlled.
Sorry to run on and on but I just wanted you to know about my experience and try to encourage you.

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Replies to "Last January I had surgery to reconstruct my spine. I had had two fusions done locally..."

I’ve been through the same thing you have but the surgeon took my pain stimulator out he said it wouldn’t help me and they don’t really work that well anyway and it’s true for me it never helped me much , I have degenerative dic disease , my family history , I had surgery four months ago a scoliosis surgery and was fused from T2to S1 with bars screws and rods and still going through my physical therapy . I’m hoping I will have a good recovery and good quality of life and somewhat pain free life , let me know if I’m asking for too much .