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Mri pml surveillance was done today ..and my jcv test came back jcv Negative tnk god 😌 so relieved it’s de best news I could hope for so unless it changes I will continue on tysabri . #grateful #greatnews #happyout #mswarrrior

I'm just sharing some thoughts here and I'm curious about other people's opinions! So, we may all know that Christina Applegate did a red carpet in the past couple days with a cane that had "FUMS" all over it. Which I respect but it's not for me. The "MSWarrior/Fighter" and the " FUMS" mentality isn...

I recently decided to start telling people I have MS. I have been very private about my diagnosis since I was diagnosed about 3 years ago. I felt like a huge weight was lifted off my chest! My friends encouraged me to go further with sharing as a healing tool. I decided to create a blog about mother...

I stumbled across this on Instagram, I’m hoping to connect with others that have this illness. I share my journey on TikTok @mswarriorantonio if you’re interested :-) I’m hoping to hear back from you all!

So in Nov 2021 I woke up with a numb bottom and foot, brushed it off that I had slept funny. Next morning symptoms worse so went to Doctors, sent to my local hospital and given an mri they did no see Anything and sent me home. Next morning woke up wobbly legs pins needles in legs, went back to hospi...

Hi everyone, I’ve had RRMS for over 20 years. I was diagnosed during a time when Australian TV was flooded with commercials of young women with MS in wheelchairs. So, when I was diagnosed naturally I assumed this was what my future held. Thankfully, I had a tribe of supporters who would not allow ...

Hi everyone! I am a new member and I look forward to making connections here. I have been diagnosed with Primary Progressive MS just over a year ago. I used to work as a Dental Hygienist (DH) and a DH educator with a college downtown. Since my diagnosis I have noticed an increase lack of balance and...

I recently found this group and am happy to be part of a community who will understand the every day life of MS. I am the daughter of an MSWarrior. My father has had MS as long as I can remember (27 years +) and I am the only support system he has. I have been struggling for the past few years as hi...

Hey! My name is Drew. I live in Louisville, KY, USA I was diagnosed in 2011, but fear I've had MS much longer. I have been wheelchair bound since 2016 and am currently on Ocrevus. Some one needs to create an app! #MSWarrior #MSStrong

40 years singing & telling story songs about NOUNS. Over 1 Million students, in schools, communities, languages, locations resulted inmy showing up. Quite a few folks with MS in the "entertainment" industries overcome like Montel, Terri Garr, Selma Blair, Annette Funnicello & Pryor stressed & miffe...

Thank you all for the birthday wishes, you sure know how to make a lady feel welcomed. My daughter and I hung out all day long. She took me to lunch at Yard House, then went to DSW for their boot and bootie sale. Then went to Kohls, then to Starbucks, then went to see Malificent 2. What a wonderful ...

Good afternoon everyone! So day 4 after my gallbladder removal, tubal ligation and endometrial ablation I say I am doing a lot better. Still have a few gas pockets but after I was able to have a BM I felt so much better. Still have some pain and soreness but its nothing I can't handle. My kids and h...

Hi guys and dolls, having RRMS at an advanced stage my disabilities are quite severe although my sense of humour and fun and love of life drive me thankfully. I've recently started a website called, www.mswarriorsandtalkmatters.com where I like to post info on my own experiences and relevant informa...