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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've made a playlist of songs that consider my fight songs that give strength and helps bring me up when feeling down. Who else has Katie Perry's "Roar" song that relates to them? I never listened to the words before but when I did it fit what I'm going through perfectly. "Eye of the Tiger" is anoth...

When I was diagnosed twelve years ago I had three lesions. Two on my brain and one on my spinal cord. My last MRI showed that the lesion on my spinal cord is gone. If only the one that disappeared was the one that causes the really bad neuropathy I suffer from. I'm on Briumvi. Not saying that it is...

I wanna share a song from my youth with all of you as a group that now I really know the meaning of it. It's called "I'm so I'm so Lucky" by Sistah Sistah. You can find it on YouTube. I'm so Lucky to be a part of a group of people going through the same things I am. Believe me. I wish that we didn'...

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. ...