Mission Stadiums for Multiple Sclerosis

Real MS Stories.
Real MS Warriors.

“My outlook for my future is wonderful. I feel like as long as I have the support of my loved ones, I can get through anything. Looking back, I feel like I learned so much after my diagnosis. You need to like and trust your doctor, you should not go to a support group until you are ready, everyone’s version of MS is different (like your fingerprint), try to always stay positive, always try to keep moving, and take help when you need it. Letting people help you takes courage.”

Alison Mannino, MS Warrior & Lead MS4MS Ambassador

My MS Story by Michael Weiss

My MS Story by Michael Weiss Donate to Michael's fundraiser here. I was diagnosed with Multiple Sclerosis in 2004 after many years of mysterious symptoms. I don’t exactly remember when the symptoms started and over the years many symptoms that I now believe were due to my MS (numbness, tingling, pain, vertigo, etc) were written [...]

My MS Story by Jennifer Jerome

My MS Story by Jennifer Jerome At the age of 39, I was working full time as a Physical Therapy Assistant in a busy orthopedic practice, running the occasional 5K and loving my life as a wife, and busy mom to 2 boys, ages 8 and 19. That fall, I ran a local 5K for [...]

My MS Story by Gus Quattlebaum

My MS Story by Gus Quattlebaum “Of course you’re limping. You walked off a seven-foot wall!” Countless doctors were taken off the scent after my accident in the fall of 2017. My accident wasn’t a result of MS, but it eventually led to my diagnosis of primary progressive MS on Christmas Eve of ’21. My [...]

My MS Story by Thom Szymanski

My MS Story by Thom Szymanski In early September 2023, I came down with a bad stomach bug. I spent all of Labor Day weekend going between the bedroom and the bathroom drinking a lot of water and hardly eating anything. By the following Friday, I finally felt recovered enough to go back to the [...]

My MS Story by Katy Haughn

My MS Story by Katy Haughn My journey with multiple sclerosis, which began in 2015, has been one of challenges, resilience, and gratitude. In the years that followed, I faced numerous relapses and tried various disease-modifying therapies (DMTs). Regular MRIs became a routine part of my life, and I focused on managing MS the best [...]

My MS Story by Mel Livermont

My MS Story by Mel Livermont My life had been composed of an over ten-year career of Firefighting/paramedics which I loved, then one day in the middle of May 2018; I started having more and more symptoms of migraines. I did not realize something severe was taking place in my body. A few months prior [...]

My MS Story by Ava O’Brien

My MS Story by Ava O'Brien Hi everyone! My name is Ava O'Brien. I am from Boston, MA and I live with my mom, dad, and two sisters. I am studying Health Policy and Management at Providence College in Rhode Island. I was diagnosed with Relapsing-Remitting Multiple Sclerosis in the early summer of 2018 when I [...]

My MS Story by Tony Nelson

My MS Story by Tony Nelson I am a 49-year-old male. Being diagnosed with multiple sclerosis (MS) in 2003 was a life-altering moment for me, filled with fear and uncertainty. I found myself hiding from others and keeping my condition a secret. I often wondered how long I could continue this silent struggle with MS. [...]

My MS Story by Adam Nelczyk

My MS Story by Adam Nelczyk In the summer of 2022, I had just turned 31 years old and was on the verge of finishing up my PhD at the University of Illinois at Urbana-Champaign. I had been in school a long time, like a really long time, and at that point it was harder [...]

My MS Story by Dominic Toupin

My MS Story by Dominic Toupin Hello all, my name is Dominic Toupin, I am 26 and an MS Warrior! All of my life I’ve been a very active person. I played Football and Baseball in high school, I trained and competed in the 2018 CrossFit Open, and was a Manager of a restaurant all while [...]