Has anyone had a abbot spinal cord stimulator put in?
Hi my name is Joe and new to the group. I have had 10 surgeries on my spine both neck and back. Now as before I deal with chronic pain worse than before all my surgeries. One big reason is scare tissue. I was wondering if anyone has had an Abbott spinal cord stimulator put in. And if it has helped? And how long you have had it installed. I’m thinking this might be my next thing to try. Would appreciate any input you could share. Thank you!
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I am so sorry to hear your frustration. To be close to Christmas, and not have the support from the Abbott staff to be there, after spending countless hours with the stimulator in your spine, and not performing at what we understand to be the magic to counter the pain is over the top.
I hope the phone number a person gave you will help. Please continue to keep this site updated on your condition.
I have had the Abbott WaveWriter since August 2023 for chronic L5 nerve damage. It has helped until just recently and now I may need another surgery. I had L4-5 fusion in 2020.
My Abbott rep responds within hours and helps me as needed. I've never had an issue with response time. I would tell the surgeon who placed your SCS that the rep isn't replying to you, they will get it handled. It's big bucks for the surgeon with minimal work. Unfortunately this is not the best time of year to get anything done.
I am waiting to find an MRI machine that can do me, otherwise I may see if we can't just do a CT. I had an arthrogram (CT with direct joint injection) of my shoulder vs an MRI prior to that surgery. I may ask if that can be done on my back vs a MRI.
I wish you luck. Pain is a problem.
@vikkitennis I have had several MRIs since having my first SCS implanted in 2017. I tend to be cold blooded, so was never too warm in the MRI tube. But this is a potential issue with any SCS and perhaps some other medical devices. During my last MRI they refused to give me a blanket due to a policy change at the imaging center. Apparently, they had some patients get too warm due to metal medical devices, even if non-ferrous, and would no longer allow blankets for imaging patients with an implanted medical device.
I haven't heard of anyone having an MRI under anesthesia, but I know it's common for doctors to prescribe a Valium tablet for patients who experience anxiety in the MRI tube. Or perhaps imaging in an open MRI system would make the experience better for you.
I talked with imaging at the Center in Phoenix, and she mentioned about MRI's in a hospital setting and placing a patient under anesthetic. I inquired about an open MRI, but that isn't possible for SCS patients. Yes, I have heard about the medication a Valium, for relaxation. As I mentioned in the past before the SCS, I have had many MRI's, and sailed through them. I believe it was due to the narrow "tube" that freaked me out after 25 minutes. I was told a CT scan is close to what the medical staff can analyze. I am to see the neurosurgeon today who implanted the SCS and discuss removing it. He is very personal, I like him, and respect him.
My friend has to anesthesia for an MRI. She has lots of sensory issues.
As I’ve said before here, if the SCS isn’t alleviating your pain & it’s causing other issues have it removed! I had the Boston Scientific SCS in 2021 & it never helped. Taking my orthopedic pain Dr’s advice, I had it removed this past February. I know it works for some, but I didn’t want a “foreign body” in my back that I continued to charge weekly & got no relief!
After much contemplation, I decided on the Abbott Burst in 12/22. Trial performed well, as many people will tell you, yet there is much research to conduct with the SCS once implanted. Burst implant was 2/2023.
epidurals, PT, not ablation (I don't know why the pain management doctor has not considered: could be due to the spinal fusion of L4-S1 in 12/2015) I went for the Abbott. I have been aware of the stimulator since 2019, but waited until much improvements and testing were performed to consider being a candidate.
The Burst was too obtrusive on my slim frame, so another surgery to insert the Eterna. That was 7/2023. Device seemed to work, had several re-programing with the reps, but didn't get to pain going down the leg. I had an MRI to further examine the demise of the spine, and discovered the levoscoiosis has progressed to a 20%, where the curve is concentrated on the left side. I am quite active, and I knew with stretching (more PT) and continue with the sports I love would keep the pain at bay. The stimulator was turned off when going through airport security in October, and I neglected to turn it back on. Oh My! it made me think there wasn't a difference, SCS or not. I met with the neurosurgeon this week, and he told me it performs for 50% of the population, and I gave it "more than a college try" of which I felt good about, and wasn't flippant and decided in two weeks to end it all. Device will be removed in February 2025, and I will go from there. I am able to play tennis, pickleball, walk and ride my bike, while lifting moderate weights. I turn 70 March 2025. What a road to the upcoming birthday!