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2,505 total results
Comments (2,285)
@american I go to University of Colorado Hospital. The neurology department has a group of doctors...
https://connect.mayoclinic.org/comment/280224/
inflammatory problems in the brain (like MS
Hello @glennaskinfolk -- Welcome to Connect. Thank you for sharing your spouse's experience. It's great advice...
https://connect.mayoclinic.org/comment/261603/
How is your spouse doing now with MS
I found the series worth it. The other presentations are also available on YouTube: Exposure and...
https://connect.mayoclinic.org/comment/328069/
Back With Food, Michelle MacDonald MS
I was wondering how long it takes to see a difference. I have just been on...
https://connect.mayoclinic.org/comment/952147/
I started with MS and now Fibromyalgia
Dear Ms. Phus, Are you suggesting that nuts are nutritious, or that it's OK that I'm...
https://connect.mayoclinic.org/comment/951510/
Dear Ms.
@whattodo You are right. I have been taking Vit D supplements for years. For my family,...
https://connect.mayoclinic.org/comment/119776/
Vit D, one even almost displaying MS
I had your day last week. Lots of pain led to lots on anxiety which led...
https://connect.mayoclinic.org/comment/188464/
ago a friend with steadily worsening MS
Hi again @txsmo sorry this conversation got side tracked. In reading a little more about CIDP,...
https://connect.mayoclinic.org/comment/238721/
more about CIDP, it sounds similar to MS ... I know when I was experiencing MS symptoms ... from my own experience of having my MS
I am brand new here and yes, the reason I am here is to try to...
https://connect.mayoclinic.org/comment/918643/
I was initially dx as having MS and ... now have been told I don't have MS
Hi , yes I am a female and only know that GBS which is what a...
https://connect.mayoclinic.org/comment/1061465/
part of the many test to determine my MS ... unfortunately it is a necessary evil for Ms
@hopeful33250 Honestly had my suspicions of MS during my 3 flare up in January but the...
https://connect.mayoclinic.org/comment/118363/
hopeful33250 Honestly had my suspicions of MS ... the doctors at did not think it was MS ... on (which I later found out is the "MS
@artscaping I am so glad you asked that question. And the answer is a resounding no....
https://connect.mayoclinic.org/comment/290577/
“medically necessary” to rule out MS
I’ve had an MRI and no MS or tumors thankfully. My TN has only been on...
https://connect.mayoclinic.org/comment/816249/
I’ve had an MRI and no MS or tumors
Thanks. In my research of HFS the cause seems to be a few things so that...
https://connect.mayoclinic.org/comment/276004/
things so that was why an MRI ruled out MS
This post goes out to Ms Hines. How are you? Did you return to the ER....
https://connect.mayoclinic.org/comment/810411/
This post goes out to Ms Hines.
I was diagnosed with MGUS and MS last year within weeks of each other. Did everyone...
https://connect.mayoclinic.org/comment/889562/
I was diagnosed with MGUS and MS last
@ess77, So happy that you eventually found an accurate diagnosis for MS and helpful treatments from...
https://connect.mayoclinic.org/comment/332615/
eventually found an accurate diagnosis for MS
It can take so long to work things out, with epilepsy and everything else. My 2nd...
https://connect.mayoclinic.org/comment/104830/
She was diagnosed with MS because they ... film and put on dilantin even though MS
I had a stroke in '19 I was left with dysesthesia all on the left side...
https://connect.mayoclinic.org/comment/594202/
I read it is what MS patients suffer ... the "MS hug"
@jtbt0406 Was a steroid treatment ever discussed with you in regards to CIDP? I see that...
https://connect.mayoclinic.org/comment/238732/
is that when I was diagnosed with MS ... (and I know MS and CIDP are different
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