Diagnosis: CIDP - Rohit's Story
Вставка
- Опубліковано 8 вер 2024
- 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
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).
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
Thank you for the inspirational story. Especially when you said it will only get better.
❤ 72 yr. Old friend with GBS. I'm Looking for answers and solutions.
I'm also GBS patient survivor
Hindi me video bna dijiye
GIDEON BIBLE
APP
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.