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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...

13 years ago today I was officially diagnosed with MS. I acknowledge this day every year for two reasons. The first is so I can say a massive thank you to the friends and family who have been there since the beginning (or joined me on the way) in supporting me on my journey living with this disease....

If you’re struggling, just remember we are at civil war with our ms, so don’t let your ms win!! #mswarriors

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...

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 ...

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...

Hey everyone! 🌟 Just wanted to share a little bit about my journey with MS. Despite the challenges, I've come to see it as my very own superpower. It's a reminder that staying positive and resilient can truly make a difference. Let's keep pushing forward, supporting each other, and spreading hope. ...

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...

I accepted the diagnosis in 2021, I processed all the whirlwinds of emotions, prayed to God, then jumped into the gym to craft my body for the ongoing WAR! What the mind commands the body shall follow! As the great CT Fletcher says “I COMMAND YOU TO GROW” #MSWARRIOR

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...