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861 total results
Comments (821)
Hello @larrymc, Welcome to Mayo Clinic Connect. I'm hoping that there are others with Anti-MAG Peripheral...
https://connect.mayoclinic.org/comment/159378/
Peripheral Neuropathy and the GBS/CIDP ... Peripheral Neuropathy: https://www.gbs-cidp.org
@cyp238ress Have you had extensive bloodwork, seen a rheumatologist to check for autoimmune illness, had a...
https://connect.mayoclinic.org/comment/1110386/
illness, had a spinal tap to check for CIDP
I begin my 5th (of 6) round of infusions tomorrow to treat CIDP. 3 consecutive/6 hr....
https://connect.mayoclinic.org/comment/661839/
round of infusions tomorrow to treat CIDP
My Abbott SCS was implanted in June, 2017. First year was wonderful! I had 80% pain...
https://connect.mayoclinic.org/comment/1041871/
several treatments in the mix for my CIDP
@gaboslastresort I would have them check your cervical spine. I had spinal cord compression and flattening...
https://connect.mayoclinic.org/comment/1096625/
You may want to look up AIDP/CIDP to
I had two neurologist that told me to quit drinking coffee. I have been diagnosed with...
https://connect.mayoclinic.org/comment/1172448/
or legs), Sjogrens, lupus, asthma, CIDP
I had the Moderna vaccine as well and developed similar symptoms. It took almost one year...
https://connect.mayoclinic.org/comment/702758/
and I finally have a diagnosis of CIDP
I have CIDP and have no luck from any of the neurologists I’ve been to. I’ve...
https://connect.mayoclinic.org/comment/313855/
I have CIDP and have no luck from any
I've had CIDP for more than ten years and have cycled through every medication various doctors...
https://connect.mayoclinic.org/comment/1099956/
I've had CIDP for more than ten ... frustrating to have to go back to the CIDP
@jtbt0406 First let me just say how sorry I am that you lost your sister. Very...
https://connect.mayoclinic.org/comment/238730/
other treatments you know about for CIDP ... like neuropathy there is no cure for CIDP
@sparshall Hi Sandy, have not seen a post by you in a while, nice to see...
https://connect.mayoclinic.org/comment/325106/
horror you face in your life with CIDP
Hello @wideawakechas; I have a CIDP, a different form, but same pain as PN. My Neurologist...
https://connect.mayoclinic.org/comment/651995/
Hello @wideawakechas; I have a CIDP,
Unfortunately nothing has helped with my CIDP. Have been on all the routine meds, and IVIG...
https://connect.mayoclinic.org/comment/1045749/
Unfortunately nothing has helped with my CIDP
My case is the same . Idiopathic and now the neurologist has diagnosed CIDP after 9...
https://connect.mayoclinic.org/comment/914234/
now the neurologist has diagnosed CIDP
That’s a good question because I still don’t completely understand what I’ve been told (or not...
https://connect.mayoclinic.org/comment/81537/
Pre CIDP diagnosis, I had neuropathy ... to a Neurologist, who
gave me the CIDP
I have tested positive for four years for the Epstein Barr virus. I am now being...
https://connect.mayoclinic.org/comment/1068197/
I am now being tested for CIDP. ... EMG/nerve conduction test for the CIDP ... inflammatory demylinating disease -CIDP
I have CIDP — chronic inflammatory demyelinating polyneuropathy, which is autoimmune — and receive 5 IVIG...
https://connect.mayoclinic.org/comment/219619/
I have CIDP — chronic inflammatory demyelinating
My 72 yr' old husband was treated for 3 months. We didn't see any change. Went...
https://connect.mayoclinic.org/comment/1023234/
neuro. said my husband did not have CIDP
I have relapsing polychondritis, RA, systemic lupus, and CIDP. My RP is the least of my...
https://connect.mayoclinic.org/comment/1094285/
polychondritis, RA, systemic lupus, and CIDP
I hear you and I'm listening. Like you, my journey began with unknown causes for serious...
https://connect.mayoclinic.org/comment/855747/
The first one suspected Cidp but her
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