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747 total results
Comments (717)
@total99 here is a discussion where members are sharing their experiences -- CIDP (Chronic Inflammatory Demyelinating...
https://connect.mayoclinic.org/comment/660276/
are sharing their experiences -- CIDP ... /connect.mayoclinic.org/discussion/cidp-chronic-inflammatory-demylinating-polyneuropathy
Discussion: Nerve biopsy test: Is it done by a neurologist or rheumatologist?
Support Group: Neuropathy
Posted: Dec 7, 2021
If your neuropathy affects your legs/feet and arms/hands, make sure you are getting a correct diagnosis....
https://connect.mayoclinic.org/comment/324197/
CIDP -- chronic inflammatory demyelinating ... CIDP is rare and often misdiagnosed. ... misdiagnosed and treated only for pain, CIDP ... As a CIDP patient, I urge you to bring ... up the possibility of CIDP with your
Discussion: Now what! Neuropathy in feet and ankles.. Numbness in hands and arms
Support Group: Neuropathy
Posted: Oct 15, 2020
@jimhd Jim, after reading your post and your doctor's statement that "CIDP is an umbrella label...
https://connect.mayoclinic.org/comment/99387/
your doctor's statement that "CIDP ... is an umbrella term that includes CIDP ... From what I am reading, CIDP is auto ... Other types of neuropathy beside CIDP ... So CIDP is just a particular type of
Discussion: Chronic Pain members - Welcome, please introduce yourself
Support Group: Chronic Pain
Posted: Oct 15, 2020
Welcome @kjwalkercidp, I'm hoping @sherlock and other members with CIDP can answer your question. I'm pretty...
https://connect.mayoclinic.org/comment/1033847/
hoping @sherlock and other members with CIDP ... "Since the beginning of my CIDP ... I have CIDP and cold temperatures are ... I ..." --- GBS/CIDP Foundation ... International: https://forum.gbs-cidp.org
Discussion: CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)
Support Group: Autoimmune Diseases
Posted: Mar 15 7:56am
@sparshall, thank you for the website reference for the GBS/CIDP Foundation. I thought I would share...
https://connect.mayoclinic.org/comment/219639/
the website reference for the GBS/CIDP ... GBS/CIDP Foundation International - ... https://www.gbs-cidp.org/
Discussion: Has anyone had IVIG Infusions for Neuropathy?
Support Group: Neuropathy
Posted: Jan 16, 2020
Hi everyone! My name is Susan and I have lived with chronic pain for a number...
https://connect.mayoclinic.org/comment/99631/
paralyzed by an autoimmune disorder (CIDP ... CIDP is a rare neuromuscular disorder ... neurologist thinks that I possibly developed CIDP ... Right now I am taking nothing for my CIDP
Discussion: Chronic Pain members - Welcome, please introduce yourself
Support Group: Chronic Pain
Posted: Nov 5, 2020
Hi Fin @fintown, Welcome to Connect. I'm not sure @dellinger is still following Connect. The member...
https://connect.mayoclinic.org/comment/716039/
members are sharing their stories of CIDP ... that you might find helpful: CIDP ... /connect.mayoclinic.org/discussion/cidp-chronic-inflammatory-demylinating-polyneuropathy
Discussion: CIDP and the Covid Vaccine
Support Group: Autoimmune Diseases
Posted: Jun 10, 2022
CIDP is a terrible disease. It affects different people in different ways, but it all comes...
https://connect.mayoclinic.org/comment/219633/
CIDP is a terrible disease. ... The GBS/CIDP Foundation has a good site ... out because it’s devoted entirely to CIDP ... neurologists consider a short-term form of CIDP ... physical therapists are unfamiliar with CIDP
Discussion: Has anyone had IVIG Infusions for Neuropathy?
Support Group: Neuropathy
Posted: Jan 15, 2020
Hello @sb4ca, There isn't a separate support group for CIDP or CVID but there are other...
https://connect.mayoclinic.org/comment/889666/
#39;t a separate support group for CIDP ... I searched using CIDP and using CVID ... here are the search results: --- CIDP ... search=CIDP --- CVID: https://connect.mayoclinic.org
Discussion: CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)
Support Group: Autoimmune Diseases
Posted: Jul 3, 2023