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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

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

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. ...

Follow me on Instagram, for us people with ms. https://instagram.com/mswarrior2023?igshid=ZGUzMzM3NWJiOQ==

I have created an Instagram, just for us with multiple sclerosis, https://instagram.com/mswarrior2023?igshid=ZGUzMzM3NWJiOQ== Thank you! 🎗🧡 We are Warriors

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'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 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 ...