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963 total results
Comments (917)
Hi , yes I am a female and only know that GBS which is what a...
https://connect.mayoclinic.org/comment/1061465/
acute autoimmune neuropathy while CIDP
The only thing that really helped was physical therapy. I went to a PT clinic that...
https://connect.mayoclinic.org/comment/912867/
I have been diagnosed with CIDP and
I was put on Metanx by one doctor. When I finally got an appointment with a...
https://connect.mayoclinic.org/comment/834817/
was caused by an autoimmune disease, CIDP
I had an Abbott Burst stimulator implanted in 2017 for pain in my feet and ankles...
https://connect.mayoclinic.org/comment/1138634/
for pain in my feet and ankles from CIDP
I was diagnosed with CIDP last summer but have had symptoms for several years. I am...
https://connect.mayoclinic.org/comment/1060891/
I was diagnosed with CIDP last summer
Hand, I get an infusion of Reclast once a year. I've had four infusions so far...
https://connect.mayoclinic.org/comment/99628/
over 13 months to be diagnosed with CIDP
Hi, I have been dealing with CIDP for about 5 years now. I have been in...
https://connect.mayoclinic.org/comment/1293618/
Hi, I have been dealing with CIDP for
My husband suffers from CIDP and has been getting Immune globulin infusions for more than a...
https://connect.mayoclinic.org/comment/1318583/
My husband suffers from CIDP and has
@coachrandy I’m so sorry to hear that you’ve been diagnosed with CIDP. But you’ve come to...
https://connect.mayoclinic.org/comment/896967/
hear that you’ve been diagnosed with CIDP
Follow up to my above post. IVIG may be having more impact than I thought. I...
https://connect.mayoclinic.org/comment/1222821/
This was of course part of the CIDP
Frances, I too get IVIG infusions. It was every 3 weeks but that last week was...
https://connect.mayoclinic.org/comment/1122629/
I have CIDP, lupus, RA, immune deficiency
@dklaus @harley22 Since both of you are dealing with the same issues I thought I would...
https://connect.mayoclinic.org/comment/1101205/
I don’t have CIDP, so really can’t compare
I’m with you. I’m experiencing the same symptoms as you, and nothing works. Gabapentin did nothing...
https://connect.mayoclinic.org/comment/1059077/
neurologist in Arizona who specializes in CIDP
I was told that either my CIDP was autoimmune, genetic or caused by something like a...
https://connect.mayoclinic.org/comment/1051160/
I was told that either my CIDP was autoimmune
@harley22 I see you have been visiting the neuropathy support group, also. Sometimes our medical team...
https://connect.mayoclinic.org/comment/943771/
Do the doctors attribute your CIDP diagnosis
You should see a dermatologist. Two neurologists have told me this has nothing to do with...
https://connect.mayoclinic.org/comment/288833/
me this has nothing to do with my CIDP
Yes CIDP and most likely from the Covid Vaccine! UCLA nueromuscular is fast and great! They...
https://connect.mayoclinic.org/comment/1100544/
Yes CIDP and most likely from the Covid
I am trying to navigate IVIG for CIDP and Medicare coverage. My wife has a Medicare...
https://connect.mayoclinic.org/comment/837920/
I am trying to navigate IVIG for CIDP
Yes, I have JUST after 13 years of all the symptoms, FINALLY BEEN DIAGNOSED WITH CIDP...
https://connect.mayoclinic.org/comment/824353/
symptoms, FINALLY BEEN DIAGNOSED WITH CIDP
Hi @lucy84 I have MCL stage 2A which was diagnosed last April. It's taken an indolent...
https://connect.mayoclinic.org/comment/817585/
However, I also was diagnosed with CIDP
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