Diagnosis: CIDP - Rohit's Story

To learn more about GBS and CIDP, please go to:
www.gbscidp.ca/
/ gbs_cidpfoundationofca...
/ gbscidpcanada
#cidp
#cidpawareness
#livingwithcidp
#cidpsupport
#cidpadvocate
#patientadvocacy
#cidpfamilies
#cidpwarrior
#gbs
#invisibleillness
#autoimmunedisease
#chronicillness
#IVIG
#ivigtherapy
#gbscidpfoundation
#gbscidpawareness
#peripheralneuropathy

[@toys2cars]

Been a year now since my diagnosis and regular IVIG infusions. Comparing myself now to myself a year ago is like comparing chalk and cheese. I am in a much better place both mentally and physically now, thanks to our wonderful NHS (UK).

[@TEPO--]

Very encouraging, thank you kindly.
I've been recently diagnosed after three years of suffering and my life slipping away in so many ways. I'm grateful that I'm finally being a bit more understood and looking forward to infusions hopely soon.
Your sharing is much appreciated,
Tara

[@aprilshealthmore8048]

Thank you for the inspirational story. Especially when you said it will only get better.

[@CheriBomzArt]

❤ 72 yr. Old friend with GBS. I'm Looking for answers and solutions.

[@devgbs3283]

I'm also GBS patient survivor

[@user-ic3qq1hk1e]

Hindi me video bna dijiye

[@ashoknayaki7776]

GIDEON BIBLE
APP

[@stevemartin3601]

Im going through almost exactly this same track.....Neurologist insists that "Its not CIDP"....then Doctor #2 says it IS CIDP....Doctor #3 says it is...but the lead doctor says no....so now I'm in year # 5 of this insanity.