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938 total results
Comments (892)
Welcome, @yvonne111. Good questions. I'm tagging fellow CIDP members like @mabelandlynne @cgrogers @lynn66618 @coachrandy @goldacharna @danawyn...
I'm tagging fellow CIDP members ... their coping strategies of living with CIDP ... around in this related discussion: - CIDP ... /connect.mayoclinic.org/discussion/cidp-support-group ... you might have to consider from pre-CIDP
Support Group: Autoimmune Diseases
Posted: Oct 30, 2024
Also they confirmed the diagnosis with a spinal tap ( easy no pain at all) and...
spinal fluid was the confirmation of CIDP ... a neurologist that is INFORMED in CIDP
Discussion: CIDP diagnosis
Support Group: Autoimmune Diseases
Posted: Jan 30 9:32am
Hello @goldacharna, I would like to add my welcome to Connect along with @dwyermw and others....
will provide some relief for your CIDP ... /connect.mayoclinic.org/discussion/cidp-having-ivig-reactions ... / — CIDP and concerns about treatment ... /connect.mayoclinic.org/discussion/cidp
Discussion: CIDP Support Group
Support Group: Autoimmune Diseases
Posted: Jul 3, 2023
@total99 here is a discussion where members are sharing their experiences -- CIDP (Chronic Inflammatory Demyelinating...
are sharing their experiences -- CIDP ... /connect.mayoclinic.org/discussion/cidp-chronic-inflammatory-demylinating-polyneuropathy
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....
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
@jimhd Jim, after reading your post and your doctor's statement that "CIDP is an umbrella label...
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
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...
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
Support Group: Autoimmune Diseases
Posted: Mar 15, 2024
@sparshall, thank you for the website reference for the GBS/CIDP Foundation. I thought I would share...
the website reference for the GBS/CIDP ... GBS/CIDP Foundation International - ... https://www.gbs-cidp.org/
Support Group: Neuropathy
Posted: Jan 16, 2020
Yes, I have CIDP. Typically CIDP patients have a lot of peripheral nerve pain but I...
Yes, I have CIDP. ... Typically CIDP patients have a lot of ... couple of years before I developed the CIDP
Support Group: Neuropathy
Posted: Sep 1, 2024
Hi everyone! My name is Susan and I have lived with chronic pain for a number...
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
Support Group: Chronic Pain
Posted: Nov 5, 2020
Testing for protein in the CSF is key for diagnosing GBS and CIDP. So the spinal...
CSF is key for diagnosing GBS and CIDP ... years later those tests confirmed CIDP ... find additional help with the GBS CIDP
Support Group: Autoimmune Diseases
Posted: Feb 23, 2024