Spinal cord stimulator support

@smithki

Yes!! Same thing here! I can’t have mine turned up past 5 or it hurts my legs and feet so bad! I turned it off and have had it off for 2 days now. I wrap my feet with 6 big patches of lidocaine with the self adhesive ace wrap.

I never had back pain until I got this SCS now I have horrible lower back pain whether I’m sitting or laying down. It gets worse if I have it turned on. So now not only do I have CRPS in my left foot and leg I have pain in my back, and it seems as though my CRPS has mirrored to my right foot/leg because the stimulator stimulates both legs! Why??? I only had an issue with my left foot to begin with😢💔

You’re so very welcome 🩷 I’m sorry you’re going thru this as well. My PM Dr is such a jerk, he dismisses me every time I see him, never believes me. I’m desperately trying to find a new PM Dr😢

I’ve had the Nevro HFX 10 for two years now to try to help control my CRPS Pain. It has caused more problems than it has helped. Has created severe lower back pain because I have to constantly arch my back to get it to work, they only works if I’m laying flat on my back when I try to sleep I can no longer sleep on my sides, it seems to be aggravating my CRPS nerve pain more than it’s helping. I have constant muscle spasms along my spine where the leads are. At my next doctors appointment I’m going to talk to them about having it removed.

I had an Abbott pain stimulator installed this year, I am 3 months in and not only am I in more pain but it seems it was the tech’s responsibility for a failure to correctly manage pain. On my last visit to the second post op visit with pain management and the Abbott Rep, they set my unit to the burst program on number 12. Not given clear instructions on how to set it I just left it on the setting that the Rep set it on.
3 months having the unit off and on I have developed nerve pain in a very embarrassing part of my body( If you know what I mean) I went back and told the pain Doc and a different Rep. the nerve pain issue that has literally altered my life, from my sleep and intimacy. They took a live X-ray of my back and said the lead wires were in the right spot but they were very much stumped on my constant nerve pain. After the X-ray the other Rep. that was not there at surgery , stopped me outstide and asked me question. The thing I told her was that I concluded the unit is hurting me .
When I turn it on I begin to have new places it burns very bad. Now it is painful all of the time. The Rep. told me to set the controller to 3 be cause 12 is way to high. Then she made a comment about stimulators set to high can burn nerves.I believe that is what has happened and now I have the same burning day and night with the unit off. I have an appointment to talk about where we go from here. If damage has been done because of the stimulator , it will be coming out and we will be talking what can be done . I would say between the Rep and the unit itself , there is some things needed to be said and done, not sure what that will entail. Has anyone had these issued????

@plakermike88 Hello friend! Yes, I do! I'm actually going to soon be getting a second one (or dual - but, both are Boston Scientific brand). My local team is great! Do you use the MySCS app, by chance? If not, I would advise it. It has very useful information, including your team members' contact info, ID card, tips, etc. I've had mine for 3 years now and I LOVE it! It has eradicated 85% of all my upper body pain, but I still need a second unit to address my lower body pain. Do you have any specific questions you want answered? I'd be happy to chat with you, if so. Feel free to PM me. 🙂