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963 total results
Comments (917)
I have CIDP and it only affects your peripheral nerves so you can probably take that...
https://connect.mayoclinic.org/comment/1131443/
I have CIDP and it only affects your
@shariday, I add my welcome. You'll notice that I moved your message to this existing discussion...
https://connect.mayoclinic.org/comment/605999/
to this existing discussion about CIDP
I am going to have my first Rituxan infusion in a few weeks. I hope it...
https://connect.mayoclinic.org/comment/1115183/
infusions that did nothing for my CIDP
I too have CIDP. The cause is autoimmunity. It was diagnosed by NCS, followed by about...
https://connect.mayoclinic.org/comment/642899/
I too have CIDP.
Hello @suziep, welcome to Connect. Thank you for sharing the diagnoses you are facing with the...
https://connect.mayoclinic.org/comment/142339/
inflammatory demyelinating polyneuropathy (CIDP ... anyone on this feed been diagnosed with CIDP
I have struggled with a form of vertigo called PPPD, Persistent Postural-Perceptual Dizziness, since 2017. https://www.ncbi.nlm.nih.gov/books/NBK578198/#:~:text=Persistent%20postural%20perceptual%20dizziness%20(PPPD,%2C%20peripheral%2C%20or%20vascular%20insult......
https://connect.mayoclinic.org/comment/1065355/
also have the auto immune disease CIDP-they
@sb4ca @goldacharna I found an article on the Science Direct site that mentions a genetic link...
https://connect.mayoclinic.org/comment/909351/
that mentions a genetic link with CIDP
Prednisone long term can cause steroid myopathy but I would urge you to consider other possibilities....
https://connect.mayoclinic.org/comment/1100066/
improving, I was then diagnosed with CIDP ... opposite I needed for my RA, SLE and CIDP
HI, I'm Carrie . I was diagnosed with CIDP and Small Fiber Neuropathy about 2 1/2...
https://connect.mayoclinic.org/comment/156820/
I was diagnosed with CIDP and Small ... finding another neurologist expert in CIDP
I have had high autoimmune markers for years. I have a strong family history of RA.(rheumatoid...
https://connect.mayoclinic.org/comment/1100749/
I am being tested for CIDP since it
I am headed for my 5th month of ivig treatments. Balance is better, muscles relaxed, small...
https://connect.mayoclinic.org/comment/1014991/
repair nerve seems quicker then large CIDP
If you have muscle weakness and/or muscle atrophy be sure CIDP has been considered. It stands...
https://connect.mayoclinic.org/comment/1000234/
weakness and/or muscle atrophy be sure CIDP
PS another blood test for MGUS should be done, a serum protein electrophoresis. It checks for...
https://connect.mayoclinic.org/comment/1046608/
My IVIG was denied for CIDP but approved
I also had a rash. Neurologist panicked and sent me to a dermatologist. Turns out I...
https://connect.mayoclinic.org/comment/954799/
I've had CIDP since 1996.
Did they diagnose you with CIDP? If so, curious what tests did you undergo to get...
https://connect.mayoclinic.org/comment/1100381/
Did they diagnose you with CIDP?
Your title indicates weakness in legs. I think that requires further investigation if there’s weakness progressing...
https://connect.mayoclinic.org/comment/1057191/
progressive weakness along with PN called CIDP
One of my local health care facilities has an infusion center. I just completed my first...
https://connect.mayoclinic.org/comment/833563/
optimistic that the IVIG will help my CIDP
iam starting the Vyvgart next week ??? I'll let you know how it works for the...
https://connect.mayoclinic.org/comment/1182773/
let you know how it works for the CIDP
IVIG takes at least six months to start working. It helps the neuropathy from progressing. Most...
https://connect.mayoclinic.org/comment/1092870/
I also have been diagnosed with CIDP
I have small fiber neuropathy and CIDP. I have taken Gabapentin for over 4 years with...
https://connect.mayoclinic.org/comment/1039074/
I have small fiber neuropathy and CIDP
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