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?
Interested in more discussions like this? Go to the Chronic Pain Support Group.
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.
Ok. Thank you for letting me know. Im still trying to figure out how this site works.
I feel the same! Wish no one had to suffer but it helps not to be alone💓
I wish that also! It breaks my heart and makes me very angry so many people are being forced to suffer through very severe, intense pain. Im going to be that one person who stands up for those who cant stand up for themselves. No one deserves to suffer in pain especially when surgeons have caused the extra pain. Im doing this alone so i want to thank you for reaching out to me! I really appreciate it❤️
I didn't do the private message correctly. I will try tomorrow. Take care and like you I want my voice to be heard! Look forward to getting in touch.
Gd night. 💖
Ok. Thank you. Ill make sure our voices are heard! You have a good night also. Ttys🩵
Don’t let your anger overcome your common sense.
I wish you well. I think it’s time to end our discussions.
I thought it was ok to talk about how i feel and about my experiences? Nothing is overcoming my common sense. I dont know where you got that from but since is not ok to talk about how i feel, then this forum is not for me. You have no idea what i have been forced to suffer through because of doctors. I have more common sense than anyone because i am forced to live in reality every day. Im not a violent person, i just wanted to talk through some of my feelings so its easier to deal with. I cant do that here apparently. Take care
I was told that I could never have a MRI or have my SDS ever removed! Do even think about it!! Good Luck! Bob
SCS big fingers