
05/30/2025
Happy World MS Day! I’ve been MIA lately because, well, it’s not a pandemic anymore and life is calling me in so many different directions that I simply don’t have as much time to skate anymore like I did in 2020. Nonetheless, MS is an everyday thing that I always have to make time for, regardless of life circumstances.
If you’re new here, I was diagnosed with Tumefactive MS almost 8 years ago and have been rolling with the punches ever since. My journey started with numbness and tingling in my hands and feet when entering a hot vehicle in the middle of Texas summer. I saw a neurologist who prescribed me every medication under the sun until I found one that worked for me—now I’m on Ocrevus, which has been working wonders for the past 4 years.
MS looks different for everyone; some of us are rolling on skates while some of us may roll on a different set of mobility wheels, but regardless of what part of the journey you’re on, we’re all rolling towards the same outcome: to find a cure to end MS forever 🧡