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2,506 total results
Comments (2,285)
thecyborgenchi, Bless you sweet lady. I understand. You have not mentioned fibromyalgia. Has that been mentioned...
https://connect.mayoclinic.org/comment/976902/
bloodwork to rule out Lupus, RA & MS
I was losing weight for awhile, but due to something different -- spastic colon, IBS-C symptoms,...
https://connect.mayoclinic.org/comment/1013417/
A dietician, Ms.
I first noticed joint pain and cracking and popping in my joints when I was an...
https://connect.mayoclinic.org/comment/692694/
are lupus or juvenile arthritis, or MS
It is a long haul! Multiple diagnoses, misdiagnoses, and everything in between. You are left fight...
https://connect.mayoclinic.org/comment/698855/
I was first diagnosed with MS at age
Hello @sjean, Welcome to Connect. I kind of worry when I see magic solutions to autoimmune...
https://connect.mayoclinic.org/comment/207072/
symptoms (not the disease) of her MS
I thought to write since I myself have faced situations like that. Presently, since November 2015...
https://connect.mayoclinic.org/comment/94295/
I met and spoke with blind, deaf, MS
@debmitchell101614 thank you for sharing. My experiences have been remarkably similar to yours. My struggle for...
https://connect.mayoclinic.org/comment/674634/
At times I’m convinced I have MS although
@happy3bhear, @lindes, @daphne52 and all In 2019, after again being told I had MS but with...
https://connect.mayoclinic.org/comment/624398/
2019, after again being told I had MS
I tried to post and it deleted it. Trying again. I, too, was diagnosed with CS...
https://connect.mayoclinic.org/comment/91041/
disease (compared with $150 mil to MS
I am 72 and just had a brain MRI wo contrast today. Already got the results....
https://connect.mayoclinic.org/comment/1005416/
that demyelinating disease, including MS
Don’t despair, Rameez! We are very fortunate these days that therapies/treatments available can keep CML ‘at...
https://connect.mayoclinic.org/comment/958220/
own wife has secondary progressive MS
Omgosh you sound like me , so crazy! And yes I’ve told my husband what you...
https://connect.mayoclinic.org/comment/1056160/
a surgeon and my Np both mentioned MS
it is indeed nearly impossible to explain the feeling and not being pain, people don't understand...
https://connect.mayoclinic.org/comment/729233/
there is not a definitive test for MS
I have exactly, and I mean exactly, the same issues. I am in Melbourne, Australia and...
https://connect.mayoclinic.org/comment/818391/
I had a brain MRI to see if I have MS
Thank you @johnbishop for linking me here! And thank you for the ANA links. It is...
https://connect.mayoclinic.org/comment/167799/
me anymore once I didn't have MS
Hi, I wanted to respond to you. I am so sorry you are in so much...
https://connect.mayoclinic.org/comment/310254/
looked for a woman that specializes in MS
@johnbishop Thanks Colleen and John! A little update about my condition since the last time I...
https://connect.mayoclinic.org/comment/256281/
was normal (no discs, tumours, or MS
@txsmo Hi Susan, back on 9/28 you mentioned that you were only being treated with gabapentin,...
https://connect.mayoclinic.org/comment/99622/
I know when I found out I had MS it
I tried to add to this conversation a few days ago, but touched the wrong thing...
https://connect.mayoclinic.org/comment/324387/
I now do Sudoku and MS Solitaire.
All of my 5 siblings have told me that Gabapentin worked well for them. Unfortunately it...
https://connect.mayoclinic.org/comment/1039059/
I started taking MS Contin and finally
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