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938 total results
Comments (892)
Yes definitely as that is the only thing I have is infusions of IVIG. I wish...
https://connect.mayoclinic.org/comment/1216183/
wish there was a support group for CIDP
@graziellaz Did they do a full neuropathy blood panel? What were the results? What made them...
https://connect.mayoclinic.org/comment/1274547/
What made them think he had CIDP which
I have CIDP and have been receiving infusions of Previgen since July. I have my 5th...
https://connect.mayoclinic.org/comment/81483/
I have CIDP and have been receiving ... I'm going to a GBS/CIDP symposium the ... a lot about stem cell therapy for CIDP
@bjbates53 Have you had this severe fatigue since you were first diagnosed? Has it gotten worse?...
https://connect.mayoclinic.org/comment/938290/
There is an ongoing CIDP support group ... /connect.mayoclinic.org/discussion/cidp-chronic-inflammatory-demylinating-polyneuropathy
I am new to this site- I was officially dx with Igm-CIDP/MGUS July 2019 by Mayo...
https://connect.mayoclinic.org/comment/238724/
site- I was officially dx with Igm-CIDP ... I was first dx with CMT/CIDP after starting ... With all the reading I have done on CIDP ... I read that CIDP has association with ... been diagnosed with cancer that has CIDP
Do you have a link to share about CIDP - chronic inflammatory demyelinating polyradiculopathy?
https://connect.mayoclinic.org/comment/1019548/
Do you have a link to share about CIDP
Yes I’m possibly moving there in the near future and will be needing a physician to...
https://connect.mayoclinic.org/comment/922938/
be needing a physician to treat my CIDP
I was diagnosed with CIDP in 2014. I was I’ll 13 months and was glad to...
https://connect.mayoclinic.org/comment/810984/
I was diagnosed with CIDP in 2014.
I'm not sure if I have CIDP or not go and read my post on Jazzy27...
https://connect.mayoclinic.org/comment/81506/
I'm not sure if I have CIDP or not
@anoyymous123 - I thought I would share the link for you so that others can read...
https://connect.mayoclinic.org/comment/1156775/
inflammatory demyelinating polyneuropathy (CIDP ... fda-approves-treatment-chronic-inflammatory-demyelinating-polyneuropathy-cidp-adults
May I ask what your cidp symptoms and if any treatments help you? Thanks.
https://connect.mayoclinic.org/comment/978393/
May I ask what your cidp symptoms and
Thank you that's what I thought. We're going to a neurologist who is an expert on...
https://connect.mayoclinic.org/comment/746307/
a neurologist who is an expert on CIDP ... that this neurologist will rule out CIDP
FDA just approved new drug by Argenex company for CIDP first NEW DRUG
https://connect.mayoclinic.org/comment/1146801/
approved new drug by Argenex company for CIDP
Any information on new CIDP Study using Dual-Target CAR-T Cell Therapy
https://connect.mayoclinic.org/comment/1152098/
Any information on new CIDP Study using
Search CIDP Centers for Excellence. The closest one to you may be in Utah. Best of...
https://connect.mayoclinic.org/comment/1031971/
Search CIDP Centers for Excellence.
Ok, after seeing this video, I definitely don't have CIDP but now a question what is...
https://connect.mayoclinic.org/comment/782961/
video, I definitely don't have CIDP
I have SLE as well, but I highly recommend you see a neurologist with the idea...
https://connect.mayoclinic.org/comment/1070606/
neurologist with the idea of ruling out CIDP ... the brain and spinal cord whereas CIDP ... wheelchair before I was diagnosed with CIDP
Hello @melody2sulp, welcome to Mayo Clinic Connect. Here's some information about Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)...
https://connect.mayoclinic.org/comment/238686/
Inflammatory Demyelinating Polyneuropathy (CIDP ... mentioned you have been diagnosed with CIDP
There is another discussion about the new drug - https://connect.mayoclinic.org/discussion/has-anyone-tried-vyvgart-for-cidp/
https://connect.mayoclinic.org/comment/1154197/
discussion/has-anyone-tried-vyvgart-for-cidp
It’s an international support org for people with GBS or CIDP. Google them. Many helpful resources.
https://connect.mayoclinic.org/comment/1144227/
support org for people with GBS or CIDP
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