Should I have the Spinal Cord Stimulator? Looking for reviews on this

Posted by denman55 @denman55, Jun 5, 2023

I have had chronic lower back pain due to lumbar spinal stenosis for over 10-years. I have had multiple therapies and procedures done - including RFA, Epidural steroid injections, a MILD procedure, acupuncture, OT/PT and Chiropractics, as well as an Interspinous spacer and nothing has helped my pain. After all of that, the physician I saw in March's only recommendation was for me to have the Spinal cord stimulator, but I am actually afraid of this and have read that there have been numerous injuries as a result of this implant, and after reviewing the booklet and watching the video I initially felt that it was just to restrictive in terms of how you could move your body. If you have had this procedure please let me know your results. Many thanks.

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Profile picture for tjjordan1 @tjjordan1

Mine is a Abbott, and I'm VERY happy with it !!! Make sure they do the trial 1st before implanting to make SURE, it will work. im VERY PLEASED with mine

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Thanks for the info!

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Profile picture for tjjordan1 @tjjordan1

Seriously? I have a spinal cord stimulator that needs to be replaced, about once every 10 years. Charging yourself up every few days would be ridiculous. There are much better products out there than that nonsense. No reprogramming unless I need it which so far in 4 years hasn't happened.

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I have a Boston Scientific Wave Writer and I need to recharge the battery every 3 days. I have it turned on all the time too.

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Profile picture for cynthi13 @cynthi13

Which SCS do you have? I am in the process of getting one implanted. It is a Medtronic. I am still researching to find the most effective one.

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Most SCS have their pros and cons. If you do a search online, you will likely find that the Boston Scientific Alpha WaveRider is the highest rated one. No quarantees with any of them. I wish you well.

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Profile picture for alexis7 @alexis7

I have a Boston Scientific Wave Writer and I need to recharge the battery every 3 days. I have it turned on all the time too.

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I figure that if a stimulator gives you decent pain relief, then it is well worth it if you have to recharge it every couple of days.

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Profile picture for tjjordan1 @tjjordan1

I wished it was for you too ! Mine is a Abbott, and the battery needs replaced about once every 10 years. Maybe find another provider who gives you a up to date excellent product, rather than a very high maintenance piece of crap. There are MUCH better products out there.

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I as well, have the Abbott Eterna. It is a smaller rechargeable spinal cord stimulator, requiring charging every six weeks. I met with the rep six times in the 1.5 years I have had it. The SCS was working well for me, and I had pain relief when rising in the morning, and also during and after exercises and sports. However, in the past month, I began having a burning pain on the lower left spinal side. I brought the dial up a bit, and I am not happy. I am to see a physical medicine doctor at Mayo in Phoenix late this week, and we will go from there. Beforehand, I saw a neurologist at Mayo last week, who was most attentative to my needs. I am taking Cymbalta, per his advice, for pain, and I will see where this takes me in one month. I had the trial for the Abbott SCS and the trial was good. I believe the scoliosis is interfering with the pain.

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Profile picture for heisenberg34 @heisenberg34

I figure that if a stimulator gives you decent pain relief, then it is well worth it if you have to recharge it every couple of days.

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What if there's a great product you don't have to mess with for 10 years ?? That's settling charging every few days. There are MUCH better products now.

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Profile picture for tjjordan1 @tjjordan1

What if there's a great product you don't have to mess with for 10 years ?? That's settling charging every few days. There are MUCH better products now.

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I would love that! Which product are you referring to? Always looking for new information.

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Profile picture for bootmaker @bootmaker

Hello everyone, I have my 1st visit to the spinal pain management department on the 7th of June. I was referred for a spinal cord stimulator. The reason I am going to the Mayo Clinic, is I can not get anywhere with the Dr's here in New Mexico. I have had a double discectomy, a laminectomy, and three spinal fusions. No one knows why about two months after my last fusion, why I am in some much pain. I have trouble walking any distance now. When I was walking a mile and a half twice a day. Any feed back on spinal cord stimulators or even a different process to help with pain, would be greatly appreciated.

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I hope you find the relief you are praying for. At my last appointment a few months ago, I learned my surgeon had just returned from training in Miami Florida to surgically remove this nerve vs burning the nerves. He said he would not be doing this procedure for a year at best. They trained on cadavers. I share this because if you have success in eliminating or lessening your pain with the ablation, it is possible there may be a more permanent surgery in the future to actually remove this nerve. Tamra

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Profile picture for bootmaker @bootmaker

Hello everyone, I have my 1st visit to the spinal pain management department on the 7th of June. I was referred for a spinal cord stimulator. The reason I am going to the Mayo Clinic, is I can not get anywhere with the Dr's here in New Mexico. I have had a double discectomy, a laminectomy, and three spinal fusions. No one knows why about two months after my last fusion, why I am in some much pain. I have trouble walking any distance now. When I was walking a mile and a half twice a day. Any feed back on spinal cord stimulators or even a different process to help with pain, would be greatly appreciated.

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I've had fusion, L4, 5, and S1. Four months post surgery it was like a pain free door opened but after about 7 months, I started having pain. After many trials and errors, it's turned out my body produced scar tissue from surgery that is pushing against my spinal cord. Scar tissue is difficult to see on an MRI. Just another possibility to eliminate. My best of luck to you.

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Profile picture for riovirgingirl @riovirgingirl

I've had fusion, L4, 5, and S1. Four months post surgery it was like a pain free door opened but after about 7 months, I started having pain. After many trials and errors, it's turned out my body produced scar tissue from surgery that is pushing against my spinal cord. Scar tissue is difficult to see on an MRI. Just another possibility to eliminate. My best of luck to you.

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I had a double fusion in 2022. My back pain is still there, but of course not as bad as when I first broke my back. I have an appointment with my pain specialist on Thursday. I want to consider the intracept surgery. I will probably always have some back pain, but I would like to be able to stand or walk for more than five minutes without pain. If an MRI doesn't show scar tissue what would?

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