@suzfuse46 I have had 2 SCS implanted. In 2009 I got the St Jude model. Amazing company and reps were fabulous to work with. However no amount of re-programming hit the area I needed. It was also not MRI compatible. Had it removed in 2013. Went back to annual MRIs, always taking opioids, doing PT, the usual. I learned there was a SCS that was MRI compatible so in 2021 I had that implanted. It’s Medtronic. I use it pretty much every day (unless I forget to charge the battery). The SCS only “distracts” your brain from the pain. It doesn’t block the pain. It’s also really only for nerve related problems, it never helps with muscular pain. I think that’s a misconception. It’s like a TENS unit but inside. My peripheral neuropathy is horrible. My SCS distracts my brain from that constant pain because the nerves are “buzzing”….if that makes any sense at all. Both surgeries for the implanting of the SCS called for a laminectomy in order to fit the paddle lead in my spine. Both times, it was pretty painful. However, nothing touches the peripheral neuropathy so I am grateful for my SCS. I’m also glad I can still have MRIs with the Medtronic unit. I have great Reps that will meet me at my pain management appointments if I need any reprogramming. Both companies (St. Jude & Medtronic) are great. My SCS is now 4 years old so I’m sure technology has greatly improved. My issues are mostly at L4-5, S1. I have lordosis and kyphosis and disc degeneration, spondylothesis, and 16 tumors (benign) with nerves growing through them. Now I have drop foot on both left and right feet. I use 2 AFOs and cane, sometimes a rollator and occasionally a wheelchair. Best of luck to you. I hope some of this info is helpful.