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961 total results
Comments (915)
FDA JSUT APPROVED NEW MEDICINE FOR CIDP CALLED "VYVGAH HYTRULO WHY NO COMMENTS ON MAYO ORUM...
https://connect.mayoclinic.org/comment/1154192/
FDA JSUT APPROVED NEW MEDICINE FOR CIDP ... WHY NO COMMENTS ON MAYO ORUM FIRST CIDP
Discussion: What do I do now?
Support Group: Neuropathy
Posted: Oct 8, 2024
Welcome, @yvonne111. Good questions. I'm tagging fellow CIDP members like @mabelandlynne @cgrogers @lynn66618 @coachrandy @goldacharna @danawyn...
https://connect.mayoclinic.org/comment/1165167/
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
Discussion: CIDP and trying to get on with life
Support Group: Autoimmune Diseases
Posted: Oct 30, 2024
Hi @jdoherty2025 I’m so sorry to hear you’re dealing with chronic inflammatory demyelinating polyneuropathy and Guillain-Barre...
https://connect.mayoclinic.org/comment/1338458/
who have similar experiences with CIDP ... ~CIDP diagnosis (Posted by @skyley ... /connect.mayoclinic.org/discussion/cidp-diagnosis ... / ~CIDP-GBS (posted by @bjbates53
Discussion: Your story, in six words
Support Group: Just Want to Talk
Posted: Jun 30 11:06am
I was diagnosed with CIDP about 1 year after my 4th Covid booster. As I had...
https://connect.mayoclinic.org/comment/1387886/
I was diagnosed with CIDP about 1 year ... believe that the booster triggered my CIDP ... 10,000 chance that I could develop CIDP
Discussion: vaccines
Support Group: Neuropathy
Posted: 2 days ago
Hello @goldacharna, I would like to add my welcome to Connect along with @dwyermw and others....
https://connect.mayoclinic.org/comment/889189/
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...
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
@bearmom, I don't have CIDP and can't imagine how difficult it is to manage the symptoms...
https://connect.mayoclinic.org/comment/1321345/
@bearmom, I don't have CIDP and ... mentioned by other members on Connect for CIDP ... search=CIDP%20symptoms. ... Have you seen the Shining Through CIDP
Discussion: CIDP and feeling like you are wrapped in wires?
Support Group: Autoimmune Diseases
Posted: Jun 6 7:37am
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, 2024
@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