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963 total results
Comments (917)
@supernat10, I can relate with your experience and symptoms. I am in the process now of...
https://connect.mayoclinic.org/comment/1037011/
neurologist to test me for MS and CIDP
I was diagnosed with CIDP about two years ago after a misdiagnosis 8 years earlier. I...
https://connect.mayoclinic.org/comment/805664/
I was diagnosed with CIDP about two
Would your local Dr be able to make a referral to Mayo for you to see...
https://connect.mayoclinic.org/comment/725631/
that I found researching online is CIDP
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 one implanted in 2017. I experienced 80% pain relief during the trial, and around...
https://connect.mayoclinic.org/comment/1015197/
pain is in my feet and ankles from CIDP
Several things stand out in your story. Did you have a Covid test done with the...
https://connect.mayoclinic.org/comment/1097062/
One that fits with your symptoms is CIDP
OK, my 71 yr. old husband has been a daily heavy whiskey drinker all his life....
https://connect.mayoclinic.org/comment/751777/
Demyelinating Polyneuropathy" (CIDP
I'm grateful to have a pain specialist who has gotten to know me well enough to...
https://connect.mayoclinic.org/comment/1126893/
It wasn't helping with my CIDP pain
I wish I got tested for covid in January but I didn't because I figured it...
https://connect.mayoclinic.org/comment/1097693/
I looked into CIDP and I don't think
I have been bounced around from doctor to doctor and have had many tests for over...
https://connect.mayoclinic.org/comment/1034978/
closely at the potential for MS or CIDP
I had an Abbott spinal cord stimulator implant in 1971, and the first year was wonderful!...
https://connect.mayoclinic.org/comment/904914/
Prednisone to slow the progress of CIDP
I can relate to your pain and frustration. For 10 yrs now I have been dealing...
https://connect.mayoclinic.org/comment/880653/
with no help and been diagnosed with CIDP
good evening nervelady-70, sounds like your pain is severe and you are not getting relief from...
https://connect.mayoclinic.org/comment/787135/
gabapentin for about 1 1/2 years for severe CIDP
@sueborfl Good evening, sorry to hear that Gabapentin did not help your neuropathic pain, I know...
https://connect.mayoclinic.org/comment/911436/
I have CIDP and I started Gabapentin
@txamo I wonder if you are taking bisphosphonates for your osteoporosis? Another Connect member, @sunnyflower has...
https://connect.mayoclinic.org/comment/238703/
Just put CIDP into the search window
I have been on IVIG infusions for about two months, every two weeks. Because of a...
https://connect.mayoclinic.org/comment/1076404/
Demyelinating Polyradiculoneuritis (CIDP
I’ve been suffering with bilateral lower body and neck weakness, tingling, some numbness, pins and needles,...
https://connect.mayoclinic.org/comment/1252561/
, have you done an EMG to rule out CIDP
I have severe axonal sensorimotor polyneuropathy SFN Can - cardiac autonomic neuropathy- they can’t do anything...
https://connect.mayoclinic.org/comment/1076392/
for my RA and they believe I have CIDP
Hi I was diagnosed with CIPD about 7yrs ago, before that my doctors thought I was...
https://connect.mayoclinic.org/comment/900297/
Besides having CIDP, I also have multiple
I have Graves (hyperthyroid) and CIDP (chronic Guillain-Barré Syndrome) which usually shows up on consent forms...
https://connect.mayoclinic.org/comment/937665/
I have Graves (hyperthyroid) and CIDP
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