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963 total results
Comments (917)
I was on IvIG infusions at home every 2 weeks for 10 years. My symptoms diminished...
https://connect.mayoclinic.org/comment/1274182/
I still volunteer with the GBS/CIDP
Hello Mary Ann @crissma, Welcome to Connect. I wasn't sure if you were referring to abdominal...
https://connect.mayoclinic.org/comment/1311269/
Inflammatory Demyelinating Polyneuropathy (CIDP
Because my original diagnosis was GBS, then CIDP, now it’s SFN (I’m waiting for punch biopsy...
https://connect.mayoclinic.org/comment/876559/
my original diagnosis was GBS, then CIDP
Hi to all! My name is Susan and I have multiple autoimmune diseases in addition to...
https://connect.mayoclinic.org/comment/99619/
I have been paralyzed by CIDP twice
Hello Trish I was diagnosed with CIDP about a year and a half ago! My first...
https://connect.mayoclinic.org/comment/799669/
Hello Trish
I was diagnosed with CIDP ... of the recommended ways to diagnose CIDP
I’ve had it for few years now, and my levels are so low that I only...
https://connect.mayoclinic.org/comment/1216533/
With everything else I have going on (CIDP
I was diagnosed with probable CIDP two and 1/2 years ago, after having progressive neuropathy in...
https://connect.mayoclinic.org/comment/710352/
I was diagnosed with probable CIDP
@kim1234: iv/ig has helped to keep my disease relatively stable. I get two infusions every three...
https://connect.mayoclinic.org/comment/806297/
immunotherapy and I believe caused the CIDP ... just aren't equipped to deal with CIDP
Regarding your Question about one doctor to cover all the issues related to immune diseases, disorders,...
https://connect.mayoclinic.org/comment/739813/
I have CIDP, Rheumatoid, Psoriatic and ... neuropathy in my feet and hands caused by CIDP
I just had my 3 month follow up for a total right shoulder replacement. I couldn't...
https://connect.mayoclinic.org/comment/891919/
relatively good health except for severe CIDP ... I just wish there were a cure for CIDP
Jeff, I don't know what to say, other than I'm sorry that you are suffering so...
https://connect.mayoclinic.org/comment/761785/
;s diagnosis and gave us a new one CIDP ... 're still not sure that he has CIDP
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 ... is that I was old when I developed CIDP
Sorry for your condition...if CIDP is caused by your autoimmune system, then plasmaphereses will work best...
https://connect.mayoclinic.org/comment/1202323/
Sorry for your condition...if CIDP is
I’m on IVIG infusions for CIDP and MGUS neuropathy. It was like a miracle for me,...
https://connect.mayoclinic.org/comment/978777/
I’m on IVIG infusions for CIDP and MGUS
I'm so sorry about your colleague. I developed sensory and motor polyneuropathy after the Covid vaccines....
https://connect.mayoclinic.org/comment/874250/
initially monitored for progression to CIDP
I have had CIDP since 2009 and it has slowly taken over my left hand side...
https://connect.mayoclinic.org/comment/856836/
I have had CIDP since 2009 and it has
Hi @suezq, Welcome to Connect. I see that you are a new member and have also...
https://connect.mayoclinic.org/comment/157439/
discussion "Anyone been diagnosed with CIDP
Hi Geneseos, I have Sjogrens too. I have neuropathy in my feet and lower leg. I...
https://connect.mayoclinic.org/comment/111394/
Have you looked at any of the CIDP literature
Hi kgitti, While I am not new to CIDP, I don’t live in America and many...
https://connect.mayoclinic.org/comment/1165874/
Hi kgitti,
While I am not new to CIDP
Hi, all. I started as a patient at Mayo last year. I see people on here...
https://connect.mayoclinic.org/comment/1035901/
My neuropathy (apparently CIDP and/or
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