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963 total results
Comments (917)
I know that the numbers aren't high for success with IVig infusions. I wish that they...
https://connect.mayoclinic.org/comment/979795/
it's slowing the progression of CIDP
I’m sorry for what you are going through…the word I keep coming up with is cruel....
https://connect.mayoclinic.org/comment/914611/
I wonder if I have CIDP but I think
I have 2 Neurologists. Both professors, with completely different ideas on IVIG. I was diagnosed with...
https://connect.mayoclinic.org/comment/1060146/
LFN was added then It was changed to CIDP ... here but prof 1 said it could help CIDP
A quick google search will tell you exactly what is CIDP -mostly caused by autoimmune system......
https://connect.mayoclinic.org/comment/1202358/
search will tell you exactly what is CIDP
I have been dealing with a wound on my right foot, on bottom of my foot,...
https://connect.mayoclinic.org/comment/1044487/
I’m assuming because of my CIDP, it
I have been getting IVIG infusions every 2 weeks for the past year. My doctor says...
https://connect.mayoclinic.org/comment/873814/
not confident that the diagnosis of CIDP
I have been to a neurologist that has taken nine months to figure out I have...
https://connect.mayoclinic.org/comment/318896/
nine months to figure out I have CIDP
Hello jhill, the nerve biopsy was one of a series of tests to confirm the diagnosis...
https://connect.mayoclinic.org/comment/1390659/
tests to confirm the diagnosis of CIDP
I was diagnosed with CIDP in 2020. I have neuropathy in my right foot and my...
https://connect.mayoclinic.org/comment/1166513/
I was diagnosed with CIDP in 2020.
There are excellent neuropathy centers with lots of experience in GBS.
The Neuropathy Association (neuropathy.org) lists...
https://connect.mayoclinic.org/comment/55500/
In addition the GBS/CIDP Foundation ... International (http://www.gbs-cidp.org
I had symptoms of CIDP for years and had normal EMGS x 3. It wasn’t until...
https://connect.mayoclinic.org/comment/1100665/
I had symptoms of CIDP for years and
What you are experiencing sounds very similar to my experience. But in addition to the testing...
https://connect.mayoclinic.org/comment/1087899/
me suspecting and confirming I had CIDP
Hi kuriousmind, my huband had cognitive decline and would fall and couldn't get up. He's 71...
https://connect.mayoclinic.org/comment/1048564/
The second said he had CIDP and so we
I have exactly the same types of shooting pains like you. Sometimes they’re in the most...
https://connect.mayoclinic.org/comment/1041607/
neurologist, and he attributes it to my CIDP
Relocating to Phoenix at some point and called Mayo Clinic for an appt. I was told...
https://connect.mayoclinic.org/comment/1031626/
finding some kind of hope with my CIDP
I’ve had lip sores from biting them for over 10 yrs now. My upper and lower...
https://connect.mayoclinic.org/comment/1029231/
I’m assuming it’s part of my CIDP ,
Hi there Bryan- I'm sorry to hear about your health issues. SPS is a member of...
https://connect.mayoclinic.org/comment/49585/
Myesthinia Gravis, Sjogren's, CIDP
Thank your help! What is CIDP? i will research it also. Is there anything that can...
https://connect.mayoclinic.org/comment/1044203/
What is CIDP?
My husband, age 71, was told he had CIDP and given infusions which didn't seem to...
https://connect.mayoclinic.org/comment/819166/
husband, age 71, was told he had CIDP
A gentle reminder that the topic of this discussion is CIDP (chronic inflammatory demylinating polyneuropathy). For...
https://connect.mayoclinic.org/comment/238715/
that the topic of this discussion is CIDP
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