Every morning! LOL j/k During the dx process I knew I was in good hands and trusted my PCP and neurologist. Although occasionally I question everything, I know that all possibilities have been exhausted. I went through quite a bit of testing for a few years trying to figure out what was going on and ultimately had the big event (major flare) that gave me the dx.

Additionally, I was in a study and the dr is a well known MS specialist in the U.S. as well as internationally. So I know if he saw something that was not consistent with MS, my dx would have changed.

While the process of dx can sometimes be long, most good neurologists don't hand that dx out lightly. Good luck with your appt. in March. Hang in there and know we are all here to support you through this.