To narrow your search, try adding quotation marks around phrases.

Search tips
  • Search by keywords or complete phrases.
  • To narrow your search, try adding quotation marks around phrases.
  • Example: "predictable behavior" will narrow the search results to only include content that has the exact phrase "predictable behavior" in it.
373 total results
Comments (358)
Hi Kim Sorry to hear that you also have been diagnosed with CIDP. I also have...
https://connect.mayoclinic.org/comment/805485/
Sorry to hear that you also have been diagnosed ... with CIDP. ... I was diagnosed in 2021 and immediately ... neuropathy but the pathophysiology for CIDP ... GIB-CIDP.org is a great organization
Discussion: Anyone been diagnosed with CIDP? It's very rare
Support Group: Autoimmune Diseases
Posted: Feb 2, 2023
I just ran across these YouTube videos that I thought might be helpful for anyone new...
https://connect.mayoclinic.org/comment/786106/
might be helpful for anyone new to CIDP ... Optimizing Outcomes in CIDP: Honing ... Diagnostic Accuracy, Personalizing Treatment
Discussion: Searching For Diagnosis. CIDP? Please Help Me
Support Group: Neuropathy
Posted: Dec 18, 2022
I have neuropathy still - year later! I started having neuropathy throughout my entire body after...
https://connect.mayoclinic.org/comment/759666/
The ER diagnosed me with carpal tunnel ... This diagnosis frustrates me to this ... knowing any better, I accepted the diagnosis ... get me to the right Dr or test for CIDP
Discussion: COVID vaccines and neuropathy
Support Group: Neuropathy
Posted: Oct 11, 2022
Good morning, I had similar issues after my Moderna vaccines. My left foot and leg had...
https://connect.mayoclinic.org/comment/670495/
challenging for providers to make a diagnosis ... providers the neurologist said I have CIDP
Discussion: COVID vaccines and neuropathy
Support Group: Neuropathy
Posted: Jan 13, 2022
Hello @mrsfitz, Welcome to Connect. While we wait for those members to share personal experience you...
https://connect.mayoclinic.org/comment/639460/
." --- GBS|CIDP Foundation International ... and Vaccinations: https://www.gbs-cidp.org ... little more about how and when you were diagnosed
Discussion: CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)
Support Group: Autoimmune Diseases
Posted: Sep 27, 2021
Specifically I have many classic symptoms of GBS / CIDP I was first diagnosed with GBS...
https://connect.mayoclinic.org/comment/604973/
have many classic symptoms of GBS / CIDP ... I was first diagnosed with GBS 4+ ... Subsequent diagnosis (though not definitive ... ), as of yesterday, is CIDP. ... and can perhaps give me a definitive diagnosis
Discussion: COVID vaccines and neuropathy
Support Group: Neuropathy
Posted: May 26, 2021
Hello @theresadono, Welcome to Connect, an online community where patients and caregivers share their experiences, find...
https://connect.mayoclinic.org/comment/603005/
Excerpt from article below – "My diagnosis ... Living Each Day to the Fullest – GBS/CIDP ... Foundation: https://www.gbs-cidp.org
Discussion: Living with Neuropathy - Welcome to the group
Support Group: Neuropathy
Posted: May 19, 2021
Totally new to this but considering most of my doctors had to research CIDP ...I was...
https://connect.mayoclinic.org/comment/602544/
most of my doctors had to research CIDP ... ...I was apparently diagnosed five ... The diagnosis explains alot. ... seem to be any scientific research on CIDP
Discussion: COVID vaccines and neuropathy
Support Group: Neuropathy
Posted: May 17, 2021
I have CIDP -- chronic inflammatory demyelinating polyneuropathy -- an autoimmune form of PN that is...
https://connect.mayoclinic.org/comment/325105/
I have CIDP -- chronic inflammatory ... But by the time I was diagnosed I had ... is that I was old when I developed CIDP
Discussion: Why test for neuropathy if there is no cure?
Support Group: Neuropathy
Posted: Nov 11, 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 ... It took doctors 13 months to diagnosis ... 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 Rachel and Hank, I have never been treated at the Mayo Clinic. I had an...
https://connect.mayoclinic.org/comment/238705/
an appointment the first year I was diagnosed ... I was diagnosed and still see a Mayo ... never mentioned a particular diet for CIDP
Discussion: CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)
Support Group: Autoimmune Diseases
Posted: Sep 30, 2020