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Implantable neurostimulator for chronic pain

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

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@jimhd

@user_chf56161a How are you feeling by now? Which stimulator did you get? Is it MRI compatible?

I had a Burst DR implant in June of 2017, had a huge amount of relief from the pain in my feet, and was told it was MRI compatible. I was all prepped for one, turned on the controller and it said MRI not advised.

I've met with the Abbott tech every three months to make adjustments, but the past 8+ months the changes have done nothing. I turned it off Sunday, August 11, the day after my 69th birthday, and I haven't felt any increase in the pain. Coincidentally I started a new medication that same day, imipramine, and I've had less pain. Maybe I've finally found a medication that I can tolerate and that helps with the pain.

I'm going to be talking with a surgeon the end of the month about a new stimulator that would be connected to my dorsal root ganglion. The Abbott tech is the one who told me about it, so I'm trying to get info from unbiased resources.

While my stimulator was working it was great, so I'm disappointed that it quit doing its job. I had hoped it would be a long term solution. Of course, this is my own story. I've read here that many people are happy with their stimulators after much longer than two years. I hope that will be true for you.

Jim

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Replies to "@user_chf56161a How are you feeling by now? Which stimulator did you get? Is it MRI compatible?..."

Thanks Jim, I have a Boston Scientific model. I do go in about the same as you for adjustments. So far so good. They are constantly making improvements, so you might want to check with your pain specialist to see if any have come out. I only had to have the battery changed out for the improvement in my condition. I am glad you found some medication that works. If something goes wrong with mine in the future, I'll ask my doc about it. Best of luck!

Hi Jim,
Just wanted to touch bases. As you know I had the Abbott Stimulator which tested good but upon installation and after 4 revisions gives me no relief.
I then had the DRG test and it was amazing. However, a few months after installation it lost its effectiveness on me also.

I’ve tried every tech in Oklahoma and now MN several times and they cannot get it to be helpful.

I’ve had them off for most of a year with tests when they try to readjust.

I was never told and did not have the initiative to find out that there were other options.

A friend asked if I had tried a Medtronic pain pump. I had to suggest it to my pain clinic and they said “yes, that sounds like a really good fit for you”. Can you believe they install them but never posed it as an option!

I had it tested and installed last January and it has been a literal life changer for me. It took a long time to get it titrated up, but it helps more than either/both stimulators combined and there is room for improvement as time goes on.

Just want to be sure you hear about the options before getting The DRG implanted.

I wish you he best of luck and am glad you found a med that helps.

Carl