Reply To: An update on Emily…a long time coming

May 28, 2015 at 8:39 am

Fantastic Kelly. Your pride in Emily is justified; she is a gifted young lady.

I’m so glad to learn Emily is treatment and symptom free. My neurologist’s goal for me was that I would get to the point that CIDP would not be the focus of my day. I can say I’ve arrived at that goal and I rarely visit the forum anymore (CIDP is just not on my mind very often if at all). Thinking back at the tremendous weight we’ve carried over the last 6 years since contracting CIDP reminds me What a burden those of us affected by CIDP carry (patients and caregivers). So I’m so glad that you’re free of the CIDP burden and not focused on CIDP on a daily basis either.

Your vigilance and hypersensitivity towards Emily’s health is wise because of the road you’ve travelled.

May God continue to richly bless Emily and you. Sending joyful cyber hugs towards you and Emily …