Relocating to Phoenix at some point and called Mayo Clinic for an appt.
I was told there were no neurological appts available at this time.
This was my last hope in finding some kind of hope with my CIDP.
I’ve been to 6-7 neurologists over the past 11 yrs with not one doc able to figure out what’s up with me, or a treatment to help my nerve pain.
Been on all the meds, IVIG infusions, and testing available including mris, spinal taps, EMGs, nerve biopsies, tests to r/o MS and Amyloidosis,etc.
Right now I take Tramadol 50 and salonpas pain patches as needed for pain.