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Implantable neurostimulator for chronic pain

Spine Health | Last Active: Jun 21, 2023 | Replies (334)

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@jimhd

@wisco50

Being a nurse, of course you understand the ramifications of the litany of treatments out there. I'm the only one of six kids who has escaped back issues that involved surgery. The only back problem I've had was compound fractures of T12 and L2, self inflicted because I bailed at 12 feet from a ladder that started a crashing slide across the back wall of my house as I was painting it. I landed in a seated position with my back against a concrete wall. It didn't hurt immediately so I finished that wall and the long side of the house, either on a ladder or a scaffold. I had the house all masked and didn't want to have to do it again. Bad choice. The ER nurses were less than happy.

Have you been given options? Fusions help lots of people, but if there's any other treatment, I'd be considering it.

My pain specialist, whom I saw a few hours ago, has been a Godsend. He's hung in with me in the decade long search for a medication that I could take safely. I think we've finally found it! I pray it will be so. And I pray that you will find the best solution for your back pain.

Jim

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Replies to "@wisco50 Being a nurse, of course you understand the ramifications of the litany of treatments out..."

OMG, I guess you managed what is called catching a lucky break (pun intended!). I don't have to tell you just how "lucky" you were, because you already know it (and likely told so by hospital personnel). Well, my options are to 1) continue as I am, above (and hope no one removes my minimal doses of hydrocodone - so far no problem with my primary MD who knows me well). It "works" but isn't optimal. 2) have the extension of my already multi level lumbar fusion (discs above the fusion are showing signs of problems, no surprise) 3) try for a more minimal but still invasive surgery "try a few screws" with no guarantee or 4) try the spinal cord stimulator if it appears to help during trial. I've tried every NSAID pill, gel, cream known and aspirin works as well with least side effects. Tried various spinal locale injections with local/steroids. Which at least helped pinpoint the problem to L4-5-S1. I do realize NO guarantees with anything of course. i just hope to not make it worse....the one thing that can give hope is that medicine advances steadily and who knows what will be offered a few years down the road? Somewhat vaguely similar to you, my primary stuck by me for most of 10 years while I dealt with unrelenting pain from serious jaw issues. Long story short, I am now 10+ years out from receiving artificial jaw joints. If it hadn't been for her and a great psychiatrist helping me, and me being a stubborn RN who knew I wasn't making things up - I also finally found (thank you, internet!) not one but two incredible oral maxillofacial surgeons who believed me, diagnosed me and ultimately fixed me (many fights with my insurance company!). So I do have faith in medicine, just need to match what's available with my needs. Fingers crossed and a prayer. I certainly wish you all the best also!