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942 total results
Comments (896)
Hi Cathy @catharbert, I'm not sure @harley22 is still following Connect but @gratefulone may have some...
https://connect.mayoclinic.org/comment/720513/
experience to share on the IVIG therapy for CIDP
I have been diagnosed with CIDP and am currently getting an IVIG infusion every 4 weeks,...
https://connect.mayoclinic.org/comment/1053220/
I have been diagnosed with CIDP and ... my trunk) are associated with the CIDP
I start Vyvgart this week. After 4 years of CIDP (Induced by the covid Vaccine) it...
https://connect.mayoclinic.org/comment/1248200/
After 4 years of CIDP (Induced by the
@nemo1 You might also find this webinar on CIDP from the Foundation for Peripheral Neuropathy helpful....
https://connect.mayoclinic.org/comment/1021517/
You might also find this webinar on CIDP
I’ve been on Gabapebtin preceding the CIDP and IVIG and periodic steroids for the CIDP a...
https://connect.mayoclinic.org/comment/1206841/
ve been on Gabapebtin preceding the CIDP ... IVIG and periodic steroids for the CIDP
@amieb mentioned CIDP and sciatica in another discussion here and may have some additional suggestions or...
https://connect.mayoclinic.org/comment/1179346/
@amieb mentioned CIDP and sciatica in
I have CIDP and have had all three Pfizer shots snd have had only mild reactions...
https://connect.mayoclinic.org/comment/652628/
I have CIDP and have had all three Pfizer
Since I posted about CIDP I have been rediagnosed with POEMS syndrome even rarer than CIDP....
https://connect.mayoclinic.org/comment/81491/
Since I posted about CIDP I have been ... with POEMS syndrome even rarer than CIDP
hello Cathy, I saw your note regarding IgG therapy for CIDP and I started IgG therapy...
https://connect.mayoclinic.org/comment/720911/
your note regarding IgG therapy for CIDP ... and I started IgG therapy for CIDP ... information helps you to manage your CIDP
If you read the available medical literature I think you will understand. GBS is a rapidly...
https://connect.mayoclinic.org/comment/1153705/
developing short term illness whereas CIDP
thanks for the welcome. thanks for the referral to the foundation for peripheral Neuropathy. Regarding the...
https://connect.mayoclinic.org/comment/782537/
Regarding the CIDP I don't know
Same. First they said CIDP. BUT when nerve and muscle biopsy done. Said no. Now saying...
https://connect.mayoclinic.org/comment/1233707/
First they said CIDP.
Thank you. I have been enjoying the posts and positive feedback. There's so much to learn...
https://connect.mayoclinic.org/comment/156825/
There's so much to learn about CIDp
I am taking Panzyga. It was approved in 2021 for CIDP. It has no glucose in...
https://connect.mayoclinic.org/comment/1144279/
It was approved in 2021 for CIDP.
No you’re not missing anything. I haven’t heard or read anything saying that Gabapentin was addicting....
https://connect.mayoclinic.org/comment/1105739/
years, and it actually didn’t help my CIDP
@paktoledo: I have a friend with Lupus and she has neuropathy in her hands and feet....
https://connect.mayoclinic.org/comment/806302/
are likely from Lupus and are not CIDP ... medically and trust me, you don't want CIDP
I have also been diagnosed with CIDP. I believe that this is because there seems to...
https://connect.mayoclinic.org/comment/984637/
I have also been diagnosed with CIDP
This is promising news, Raphy, especially for patients who are immunocompromised. I moved your post to...
https://connect.mayoclinic.org/comment/661049/
to this existing discussion about CIDP
Mark, Mayo turned me down too. But I’ve had excellent care for my CIDP in Albuquerque...
https://connect.mayoclinic.org/comment/1210933/
But I’ve had excellent care for my CIDP
Yes I was diagnosed with CIDP 7 years ago. When I was 16 I was diagnosed...
https://connect.mayoclinic.org/comment/81481/
Yes I was diagnosed with CIDP 7 years
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