Even though I have CIDP, I think I can still relate. I am healing and recovering and I’ve gone back and forth about whether I still need a neurologist. It makes sense to me that I should only go to one if I show signs of a relapse. I am changing family doctors for the third time and the new one shows promise of wanting to learn about CIDP. That’s enough for me.
Rather then a neurologist, what I want is a doctor that has a knowledge of rehabilation and physical therapy because I need to learn how far to push myself in a recovery.