Spinal Cord Stimulator Removal
My Medtronics SCS stopped working after about three years. A NEVRO rep talked me into having one of theirs implanted. They had to use an adapter to connect Nevro unit to Medtronics lead. As a result, I cannot have an MRI. Also, the Nevro did not help at all. I would like to have all the SCS stuff removed (or, at least, the NEVRO battery replaced with a Medtronics) so I can have the MRI that my pain specialists seem to want very badly. Anyone out there have this experience this?
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Please be very careful getting it removed. Make sure the surgeon has experience and has great reviews. I know its very nerve racking but research is your best option right now. I didnt know it at the time but the surgeon did not have any experience removing a NSS. Please be careful. Look what happened to me. If you want to talk, im here for you.
It breaks my heart to hear that. I am so sorry. Doctor now a days are not doctors. All they care about is money. Since my severe car accident in 2018, i learned very quickly how to read MRI's CT's, X-Rays, bloodwork, etc...I actually know more than 98% of doctors now and they do not like me because i know more than them. I stand up for myself, Im my own advocate. Doctors dont like that either. They are not God. I tell them all the time and they dont like that either. Oh well! Im fighting for my life and Im very bluntly honest. Thats all I can be.
I hope your husband is doing better. The lumps in his back was probably spinal fluid like i had. Your husband is a fighter and a survivor of this crooked health care system.
I would like very much if you would contact me privately. I have suffered more horrifically than I can convey on this forum but your situation has been so much worse and bring me to tears, what you have
been thru is beyond understanding. Im so sorry.
I am very traumatized as i am sure you must be, i am starting therapy. Its as you say, the disgraceful way Drs treat our bodies. I find the support here very comforting. You absolutely need a lawyer. Its never about the money, its about warning people of the terrible side effects.
Pls reach out privately, you absolutely need compensation for your situation. You are not alone in your struggle to regain your health...Pls know this. Huge hugs , stay strong.
I had my battery removed after 12 years. I left the paddle in. I was having strange symptoms. They said my body was rejecting the battery. I'm sure it was leaking. I would have the worst night sweats. Changing my pajamas three times a night. The very first day after it was taken out they stopped. I'm sure that battery was putting poison in my body! I'm so glad it's gone.
Im new here so i dont know yet how to message privately. Can you plz message me? I understand the need to have private conversations. I am very tramatized after that. Plz message when you can. Sorry i dont know how yet. Thank you
So you didn’t have the battery replaced? Just removed? I guess after your experience, you probably didn’t want any more junk in your body.
How’s your pain level these days?
If you don't feel comfortable to confirm we'll figure out another way.
Im tied up for the next few hours but will be in touch early evening. Im hopeful by supporting each other/ exchanging info. We might be able to make some progress.
I'm deeply affected by your story. My own has me devastated, and yours has me outraged on your behalf.
Talk later...stay strong...it will get better🙏
And yes the Trauma runs deep...I get it. Hugs.
@hazel73, as a new member, you do not yet have the ability to send a private message. However, you can receive a private message from @anniesezu812.
Please do not share your emails addresses on the public forum.
Be safe when taking conversations beyond the moderated forum.
I had already done s battery replacement. Before it was removed I had a tremendous amount of pain in the battery site. It's so much better now! I'm on a better pain management plan. I realize that the battery was just a diversion. I now use other things like music, gardening, playing with my 9-year-old grandson, and my little toy poodle as diversions. I also take a edible everyday. All of those things bring me above the pain. Trying to get the pain quieter than the things you love and enjoy has been a real eye opener. I guess that's what cognitive therapy is. I just taught myself.
I just looked up how to private message and because im still a new member, it wont allow me to private message. I dont understand that but we can chat more when it allows me to accept and/or request private messaging. I think we have a lot to offer each other information wise from our experiences. I have a lot more going on and its a lot for me to write about all at once. Im actually recovering from a recent major surgery which is not going well. Im in a lot of pain and caught the flu so im not feeling to well right now. Ill keep checking to see when i can request or get a request from you to private message. It will really help to have someone to talk to and understand what im going through and hopefully for you too. Thank you for reaching out to me! Talk soon.
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