On December 19, 2023, I was diagnosed with Relapsing Multiple Sclerosis. I had no idea what my future would look like. I felt lost for a short time, I asked why me. I quickly turned those feelings into researching and learning all I could about MS, studying not just how to live with MS, but how to live better than I did before MS. I took on challenges, I changed and I navigated the best way I knew how.

The first couple of months after my diagnosis, I was hesitant about how, or if I even wanted to share my story. I did not want to be thought of as different, or less than who I once was. Fast forward to today, I will stand on every stage, in front of thousands, proud of who I am. Proud of the skin I live in, sharing the power I have gained through listening to my body more deeply, evolving with grace, and embracing each day with strength and courage to fight.

Positivity is my compass — it is the #1 thing that continues guiding me forward. I consider it a gift, not a burden, to walk this path with Multiple Sclerosis.

Helping people and being someone others can count on is what fuels me. Staying active, confident, and in motion is what allows us to live a healthy life. This mindset has been my most powerful ally. And that is how MoshenS was born! When we choose optimism, we take back control of our health and our life.

I am a firm believer that everything happens for a reason. And my reason has become clear: to spread awareness, inspire change, and bring people together through drive, resilience, hope, and Moshen.

Whether you're living with MS or another diagnosis, walking beside someone who fights every day, or honoring the memory of someone gone too soon — you are part of this story. This is more than a journey. It’s a movement to change the world.

Together, we are creating awareness that leads to action — and action leads to a cure for all life-altering conditions.

Let’s move forward, and make MoshenS together. 🎗