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Comment
@slavichx Like Colleen, I did not notice your post when you placed it here on 9/15....
Interestingly CIDP came up in two other ... One person with CIDP, @sparshall , said ... that it is very important to have the diagnosis
Support Group: Neuropathy
Posted: Oct 15, 2020
Comment
If your neuropathy affects your legs/feet and arms/hands, make sure you are getting a correct diagnosis....
make sure you are getting a correct diagnosis ... CIDP -- chronic inflammatory demyelinating ... CIDP is rare and often misdiagnosed. ... As a CIDP patient, I urge you to bring ... up the possibility of CIDP with your
Comment
Hi @10987654321, I moved your most recent message to the discussion you started earlier to keep...
that you are making progress in your diagnosis ... further with your investigation of CIDP ... idiopathic-progressive-polyneuropathy/ - CIDP ... /connect.mayoclinic.org/discussion/cidp-chronic-inflammatory-demylinating-polyneuropathy
Support Group: Neuropathy
Posted: Aug 29, 2020
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I’ve never had an MRI related to my neuropathy. I have CIDP and was told nothing...
I have CIDP and was told nothing having ... I was diagnosed via a markedly abnormal
Support Group: Neuropathy
Posted: Jan 18, 2020
Comment
Rachel, I developed CIDP symptoms in 2016, but wasn’t accurately diagnosed until late December because doctors...
Rachel, I developed CIDP symptoms in ... 2016, but wasn’t accurately diagnosed ... few doctors have ever seen a case of CIDP ... He has treated a lot of CIDP patients
Support Group: Neuropathy
Posted: Jan 15, 2020