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963 total results
Comments (917)
I have suffered from intractable hiccups for years, lasting several hours, very painful and sometimes ending...
https://connect.mayoclinic.org/comment/1072522/
Interestingly I have CIDP too.
Hi there, thanks for your in depth reply....very interesting. I think it started with stress. Initially...
https://connect.mayoclinic.org/comment/874187/
see a professor who specializes in CIDP
Hello @theresadono, Welcome to Connect, an online community where patients and caregivers share their experiences, find...
https://connect.mayoclinic.org/comment/603005/
Living Each Day to the Fullest – GBS/CIDP ... Foundation: https://www.gbs-cidp.org
Don’t have what you have, but wait til you hear my story. I have MGUS and...
https://connect.mayoclinic.org/comment/1261275/
I have a lot more with my CIDP going
Did the rituxan end up working? I was diagnosed with GBS in September 2024 after having...
https://connect.mayoclinic.org/comment/1202240/
suddenly the doctors think I have CIDP
Hi @loriesco The results we negative. So good thing there but it still means than my...
https://connect.mayoclinic.org/comment/1152296/
wrong guesses of his) that I have CIDP
I have relapsing polychondritis, RA, systemic lupus, and CIDP. My RP is the least of my...
https://connect.mayoclinic.org/comment/1094285/
polychondritis, RA, systemic lupus, and CIDP
My 72 yr' old husband was treated for 3 months. We didn't see any change. Went...
https://connect.mayoclinic.org/comment/1023234/
neuro. said my husband did not have CIDP
I have CIDP — chronic inflammatory demyelinating polyneuropathy, which is autoimmune — and receive 5 IVIG...
https://connect.mayoclinic.org/comment/219619/
I have CIDP — chronic inflammatory demyelinating
The pains in your legs and arms could be peripheral neuropathy which is caused by several...
https://connect.mayoclinic.org/comment/1038423/
things, an autoimmune disorder called CIDP
Good afternoon, I am so very sorry your Dads condition has deteriorated. Many times IgG therapy...
https://connect.mayoclinic.org/comment/739321/
with his neurologist that it is the CIDP
I begin my 5th (of 6) round of infusions tomorrow to treat CIDP. 3 consecutive/6 hr....
https://connect.mayoclinic.org/comment/661840/
round of infusions tomorrow to treat CIDP
So I am newly diagnosed with CIDP (Mid March). I am going through IVIG. I'm struggling...
https://connect.mayoclinic.org/comment/1064239/
So I am newly diagnosed with CIDP (Mid
@mothermary1 I am glad you have some level of acceptance of the reality you are facing....
https://connect.mayoclinic.org/comment/1042819/
damage assessment, spinal tap for CIDP
Welcome @sunflowergirl050710, It's difficult not to worry about a treatment when you are not sure of...
https://connect.mayoclinic.org/comment/854530/
/connect.mayoclinic.org/discussion/cidp-having-ivig-reactions
Hi Lori, thanks very much for your message! Being at Mayo was very encouraging. After my...
https://connect.mayoclinic.org/comment/746600/
I'm also dealing with a CIDP diagnosis
Ok, here goes...my husband after seeing 4 neurologist was given the diagnosis of Distal axonal sensory...
https://connect.mayoclinic.org/comment/910729/
had him taking IVIG infusions for a CIDP
Becky, I have seen 5 neurologist in both private to large hospital settings . I go...
https://connect.mayoclinic.org/comment/615189/
CIDP was not supported by neuro ultrasound
I’m 73 and am dealing with similar symptoms as you. I’ve been dealing with this for...
https://connect.mayoclinic.org/comment/1252728/
I also have MGUS along with the CIDP
@sb4ca oh my gosh! Vasculitis too! I was diagnosed with Polyarteritis Nodosa in 2016. That’s when...
https://connect.mayoclinic.org/comment/911991/
didn’t tell me anything about the CIDP
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