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1,033 total results
Comments (983)
I too had a protein level 4x higher than normal range. Got no answers as to...
https://connect.mayoclinic.org/comment/939896/
I was diagnosed with CIDP few years
I have a similar situation. My mother is 89 and I am 65. I have 3...
https://connect.mayoclinic.org/comment/1306172/
was diagnosed 2-1/2 years ago with CIDP
Wascaly, I too am 74, with severe peripheral neuropathy from CIDP, an autoimmune disease. I have...
https://connect.mayoclinic.org/comment/1164991/
severe peripheral neuropathy from CIDP
@colleenyoung Hi Colleen, yup, I agree, as far as not respecting the original topic of the...
https://connect.mayoclinic.org/comment/323960/
CIDP discussion - got a lot into God
I had my first round of IVIG infusions Oct, Nov and Dec, over aa period of...
https://connect.mayoclinic.org/comment/219630/
takes awhile to see if it’s helping my CIDP
About ten years ago I was diagnosed with PN due to slight sleepy feeling in finger...
https://connect.mayoclinic.org/comment/1135051/
neurologist who, after many tests, diagnosed CIDP
Started about 10-12 yrs ago with pins and needles in my one foot and then went...
https://connect.mayoclinic.org/comment/1127848/
of my issues I was diagnosed with CIDP
@artemis1886 You sound like me! I do not have the tremors (yet) but have had EBV...
https://connect.mayoclinic.org/comment/1068284/
testing and spinal tap to check for CIDP
I was on vyvgart for 4 weeks and in those four weeks went from weak to...
https://connect.mayoclinic.org/comment/1272901/
from weak to weeker in my legs, my CIDP
@sparshall All of my symptoms are bilateral. Idiopathic small fiber peripheral polyneuropathy has been the label....
https://connect.mayoclinic.org/comment/324199/
when I asked the neurologist about CIDP
FWIW, I’ve found that though you can’t repair the nerve damage, with regular PT (find one...
https://connect.mayoclinic.org/comment/1049613/
that knows MS if no experience with CIDP
Wow! You certainly have a large family! That can also be a stressor. And I certainly...
https://connect.mayoclinic.org/comment/218807/
very rare autoimmune disease called CIDP
@sb4ca Everything you have written about sounds like an autoimmune problem to me. Do you see...
https://connect.mayoclinic.org/comment/1034553/
can't say for sure that it is CIDP
My symptoms started about 5 years ago with cold feet. Over the course of about 2...
https://connect.mayoclinic.org/comment/662081/
again and indicated I actually have CIDP
Hi Amy, we’re not medical professionals in the Connect forum but we can rely on our...
https://connect.mayoclinic.org/comment/667567/
anything that may spur a new reaction CIDP
Oh my god. Are you me lol? I have one of the exact same theories and...
https://connect.mayoclinic.org/comment/897651/
still semi convinced I have MS or CIDP
How long did you have IVIG (gamma goblin). It keeps neuropathy from progressing and normally helps...
https://connect.mayoclinic.org/comment/1060074/
2018 and now they are checking me for CIDP
MAG level of 1418 versus normal range of 0 to 999. Other MAG bloods were classified...
https://connect.mayoclinic.org/comment/953605/
suggest axonal poly neuropathy, not CIDP
Yes, have auto immune neuropathy cidp. Hands and feet unbearable pain. Took very long to diagnose.....
https://connect.mayoclinic.org/comment/92561/
Yes, have auto immune neuropathy cidp
@goldacharma Hello, I would be glad to answer any questions relating to my symptoms, diagnosis and...
https://connect.mayoclinic.org/comment/893395/
symptoms, diagnosis and treatment of CIDP
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