Reply To: Spinal Cord Stimulator – SCS Part 15

Terri Harris

Hi everyone! As a ‘tingler in waiting’ with a rare congenital syndrome, I’m used to often being more knowledegable about my medical diagnosis than the doctors. I’m so pleased that you guys support one another, as I’ve left messages for the Specialist Nurse to answer my questions on numerous occasions, and I feel she is too busy to respond. I didn’t realise that life with SCS is so fraught with issues, as I was basically told no MRI no Airport Scanner, no Diathermy, otherwise no problem! Glad I have the time to do a little more research before my op! Hope you are all tingling well!