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860 total results
Comments (821)
Hi Ray and welcome back! Wow, you have been through the wringer and I am so...
https://connect.mayoclinic.org/comment/1068701/
My PN is from CIDP, autoimmune.
CIDP stands for chronic inflammatory demyelinating polyradiculopthy, which is why it’s always abbreviated, ha. It’s an...
https://connect.mayoclinic.org/comment/1045995/
CIDP stands for chronic inflammatory
Hello @jansendscards I have a different rare form of PN (CIDP) but many symptoms in common...
https://connect.mayoclinic.org/comment/652002/
have a different rare form of PN (CIDP
Thanks fir welcoming me. I have had cidp for 16 years, my neuropathy is unexplained...have been...
https://connect.mayoclinic.org/comment/158110/
I have had cidp for 16 years, my neuropathy
@txsmo Hi Susan, back on 9/28 you mentioned that you were only being treated with gabapentin,...
https://connect.mayoclinic.org/comment/99622/
You said you were diagnosed with CIDP
Gila, I live in Fountain Hills just east of Scottsdale. My PCP referred me to Mark...
https://connect.mayoclinic.org/comment/1009708/
peripheral neuropathy to rule out CIDP
All of my 5 siblings have told me that Gabapentin worked well for them. Unfortunately it...
https://connect.mayoclinic.org/comment/1039059/
Unfortunately it didn't help my CIDP
I get it! I don't think I can even guess how many medications, therapies, pain specialists,...
https://connect.mayoclinic.org/comment/1105050/
I have CIDP with burning pain in my
@cyp238ress I would only consider surgery if you would be able to decompress spinal cord/nerve roots/nerves...
https://connect.mayoclinic.org/comment/1110835/
If CIDP is a possibility, you may need
Hello Todd, I am so sorry to hear about your diagnosis! First and foremost in this...
https://connect.mayoclinic.org/comment/800311/
I have CIDP and I started out on 300mg
Hello @harley22. Welcome to the conversation. I believe you are responding to me @rwinney? I have...
https://connect.mayoclinic.org/comment/313856/
do have heartfelt sympathy for your CIDP
Hello @mayor47 and @vander626, I would like to welcome you both to Connect and thank you...
https://connect.mayoclinic.org/comment/81508/
treatment or what helps with your CIDP
I did 3 rounds of plasmapheresis while in the hospital & rehab last summer & fall....
https://connect.mayoclinic.org/comment/1036187/
downs, the diagnosis was changed to CIDP
We do sound alike. Cervical Fusion from seizures. Oh neuropathy can cause seizures out of no...
https://connect.mayoclinic.org/comment/1068330/
checking to see if it has progressed to CIDP
Dailyhope, coping with an illness like this is a huge challenge, I am sure for all...
https://connect.mayoclinic.org/comment/1046604/
CIDP for probably 12-15 years, but Guillain
Hello all, My heart goes out to each of you! I truly understand, I received a...
https://connect.mayoclinic.org/comment/763672/
One and a half years ago I developed CIDP
Upcoming webinar of interest... Foundation for Peripheral Neuropathy Webinar: Hereditary Neuropathy & Genetic Testing Thu, Oct...
https://connect.mayoclinic.org/comment/749431/
inflammatory demyelinating polyneuropathy (CIDP
Good morning Lori, Just read your response and you’re absolutely right, no one wants to be...
https://connect.mayoclinic.org/comment/279763/
CIDP is also known as Chronic Inflammatory
After 12 years of chasing the root cause of my symptoms, I was finally diagnosed with...
https://connect.mayoclinic.org/comment/859788/
symptoms, I was finally diagnosed with CIDP
Why thank you for even noticing that Jennifer! Yes, when I see the neurologist I do...
https://connect.mayoclinic.org/comment/1036180/
All that was part of my CIDP diagnosis
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