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860 total results
Comments (821)
Good morning, In response to your post, I have been receiving IgG infusions for over a...
https://connect.mayoclinic.org/comment/807547/
I was diagnosed with CIDP and I had
In August 2019 I had an acute onset of GBS, thought to be related to campylobacter...
https://connect.mayoclinic.org/comment/650934/
thought that my GBS had morphed into CIDP
Hi All, my story may or may not be of any note but here it is....
https://connect.mayoclinic.org/comment/876938/
Second neurologist said he had CIDP
I had the positive test in early 2021 after symptoms of CIDP and the positive nerve...
https://connect.mayoclinic.org/comment/1047067/
test in early 2021 after symptoms of CIDP
I was only recently diagnosed with CIDP, but I have had it for over 13 years!!...
https://connect.mayoclinic.org/comment/859785/
I was only recently diagnosed with CIDP
@kevinversace55 If you haven’t had a neurologist test you with EMGs, nerve conduction studies, MRIs, MRNs...
https://connect.mayoclinic.org/comment/1049912/
I need to be tested for MS, CIDP, MSA
Hello Yes, I was diagnosed with CIDP about 10 months ago and have been receiving IgG...
https://connect.mayoclinic.org/comment/730428/
Hello
Yes, I was diagnosed with CIDP ... great group to follow or join GIB-CIDP.org
I just joined Connect, and saw your post in another string about your post-infusion arm pain....
https://connect.mayoclinic.org/comment/81488/
I was diagnosed with CIDP in September
@harley22 I have the same symptoms. My journey has been 12 years, too, but significant symptoms...
https://connect.mayoclinic.org/comment/1045773/
about if I get diagnosed with MS or CIDP
I would be interested to know if your mom has any numbness in her toes, feet,...
https://connect.mayoclinic.org/comment/1092658/
I have CIDP, an autoimmune form of peripheral
My Fiance was diagnosed with cidp 20 pluss years ago his first hospitalization was a couple...
https://connect.mayoclinic.org/comment/667560/
My Fiance was diagnosed with cidp 20
When I was diagnosed in late 2020, I was hospitalized by my Neurologist so that the...
https://connect.mayoclinic.org/comment/1049626/
Once CIDP was confirmed they blasted
Hi, everyone. I haven't done the AIP diet per se, but I'm looking into what anti-inflammatory...
https://connect.mayoclinic.org/comment/1044591/
inflammatory demyelinating polyneuropathy (CIDP
I also a very disappointed that Mayo isn’t taking any new neurology patients. I have been...
https://connect.mayoclinic.org/comment/1117638/
I have been diagnosed with CIDP as far
I feel for you, as I have similar symptoms and been dealing with them for 7...
https://connect.mayoclinic.org/comment/279756/
and I’ve just been diagnosed with CIDP
@imagine1 Hello Dawn, I read your post and first I want to say I am sorry...
https://connect.mayoclinic.org/comment/872939/
experience with gabapentin, I have CIDP
I gave Buprenorphine a try for over a year, hoping I could switch to that from...
https://connect.mayoclinic.org/comment/1028407/
't start with an opioid for my CIDP
I just happened on this discussion and have learned a lot about my own hammertoes. I...
https://connect.mayoclinic.org/comment/1021358/
Because of my CIDP, I'm pretty picky
My 72 yr. old husband had been a heavy drinker all his life. Maybe drank 2...
https://connect.mayoclinic.org/comment/913303/
#2 who said rare genetic disease, CIDP
Since I was diagnosed with sfpn or CIDP, I've seen neurologists, pain specialists, a pain therapist...
https://connect.mayoclinic.org/comment/966206/
Since I was diagnosed with sfpn or CIDP
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