My story began around the 2026 New Year when I started noticing vision loss in my left eye along with numbness in my feet and legs. I ignored the symptoms for weeks, convincing myself it was just from the cold weather. At the time, I had started preseason training for my third season of college softball at Ashland University, and my body was fighting me every step of the way.

One day at practice, we were doing a running and ball-tracking drill when my vision became completely distorted, my legs went numb, and I genuinely thought I was going to pass out. Even though it was terrifying, I chose not to say anything in the moment. Looking back, that was a major wake-up call for me. Later that night, I decided it was finally time to see a doctor. After an unsuccessful emergency room visit, I went to an optometrist the following day. She asked if I had any family history of Multiple Sclerosis. After telling her I did not, she recommended I speak with my primary care physician about getting referred to neurology.

Following that appointment, I began researching MS extensively. As an Exercise Science major, I had some background knowledge about the disease, but I did not fully understand how wide-ranging the symptoms could be. Suddenly, all the puzzle pieces started coming together, and MS was constantly on my mind.

I waited about three weeks to see neurology and another two weeks for my MRI. Sure enough, they found multiple lesions on my brain and spinal cord. On March 2, 2026, I was officially diagnosed with Multiple Sclerosis. While the diagnosis was devastating for both me and my family, there was also a sense of relief. We finally had answers for why my body had been struggling the way it was.

My first thought was: how does a 21-year-old college athlete who prioritizes health and fitness suddenly develop a chronic autoimmune disease? And how will this affect my future? Following my diagnosis, I was started on steroids almost immediately, which helped manage many of my symptoms. Before long, I was able to begin practicing and playing softball again. Adjusting to life with MS while continuing to compete at a high level has not been easy, but I was determined not to let MS control my life. Some days have been harder than others, but I am incredibly proud of how far I have come. Determination truly goes a long way. I went from sitting out and thinking I might have to medically retire, to competing in our conference championship and the NCAA tournament. That experience showed me just how resilient the human spirit can be.

Although some days are still physically difficult, I constantly remind myself how blessed I am to share my story with others. I enjoy opening up about my experience and having honest conversations about life with MS. While this journey is not how I imagined my life would look, Ibelieve MS has challenged me to grow in ways I never expected and has made me stronger in the process.

I discovered MS4MS through Instagram after reading several inspiring MS stories. I was immediately drawn to the organization because of its impact within the sports community. After reaching out to Sam and having a great conversation, I knew this was the perfect place for me to continue growing, advocating, and connecting with others through my journey with MS.