Samantha Moran

I’m walking because I'm an MS Warrior!

In 2013, I was diagnosed with Multiple Sclerosis at only 20 years old. I've been living with MS for twelve years now. This auto-immune disease impacts my life daily. As an author, dysesthesia and numbness severely limit my ability to write my books and attend signings. As a parent, fatigue, migraines, and dizziness make it harder to care for and play with my children. As a partner, all of these things and more impact my ability to fulfill tasks that keep our marriage and my family strong.

And yet, MS isn't winning.

Every day, I fight back against my body to power through both the challenges I know are coming and the ones I can't predict. I use my platform to spread awareness of this disease and raise funds for a cure.

I keep going.

So, join me in this battle against Multiple Sclerosis, a condition that affects nearly 1 million people in the U.S.. We each have the power to make a difference for MS Warriors and those closest to them. 

Walk MS is an experience that brings friends and family together to show support and solidarity for people like me. No one should have to face this disease alone. 

Every dollar raised through your donations fuels cutting-edge research and provides critical services that allow those affected by MS to live their best lives.

Are you ready to make a difference? Donate today and help me reach my goal. 

Let’s put an end to MS forever.