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262 total results
Comment
I have been on Repatha for over 6 years. Repatha is suggested to be used with...
https://connect.mayoclinic.org/comment/1508278/
was diagnosed with PN in 2019 and CIDP ... My main CIDP symptom is feet numbness ... connection between Repatha and PN or CIDP ... symptoms but I did read about 2 cases
Comment
Welcome @kjwalkercidp, I'm hoping @sherlock and other members with CIDP can answer your question. I'm pretty...
hoping @sherlock and other members with CIDP ... symptoms, I have gotten chills every ... I have CIDP and cold temperatures are ... I ..."
--- GBS/CIDP Foundation ... chills-anyone/
Have you discussed the symptoms
Comment
Rachel, I developed CIDP symptoms in 2016, but wasn’t accurately diagnosed until late December because doctors...
Rachel, I developed CIDP symptoms in ... December because doctors kept saying my symptoms ... few doctors have ever seen a case of CIDP ... He has treated a lot of CIDP patients ... and recognized the symptoms on the
Discussion
Could this be CIDP
Could this be CIDP ... Could this be CIDP? ... Fast towards 3 years with same symptoms
Comment
I was diagnosed last August with Guillain Barre Syndrome following a Covid infection and subsequently diagnosed...
infection and subsequently diagnosed with CIDP ... The CIDP symptoms had been going on
Discussion
Has anyone with CIDP had Knee replacement?
Has anyone with CIDP had Knee replacement ... I have CIDP and diagnosed in 2018. ... administer myself weekly. most of my symptoms
Discussion
Ocular Myotonia VS Myasthenia Gravis
anyone been initially diagnose with CIDP ... Husbands symptoms all eye movement related
Comment
I had IVig infusions for over 2 years but had to stop in February because I...
couldn't sense any change in my CIDP ... symptoms, but I suppose it's possible
Discussion
CIDP diagnosis after severe GBS long ago, where do I start?
https://connect.mayoclinic.org/discussion/cidp-diagnosis-after-severe-gbs-long-ago-where-do-i-start/
CIDP diagnosis after severe GBS long ... results from 2020 and have most of the symptoms ... I've contacted the GBS/CIDP Foundation ... That's right CIDP diagnosis is a big ... I'm researching symptoms, how to interpret
Discussion
Anyone ever had face and limb sensory symptoms?
Anyone ever had face and limb sensory symptoms ... I have a confirmed dx'd of CIDP ... I've never had sensory symptoms
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