I was diagnosed with a rare type of multiple sclerosis called Tumefactive Multiple Sclerosis (TMS) in 2018. Back then, there were rarely any research on this type of MS and till this day, there still isn't much. I vowed that once I got better, I will try my hardest to not only spread awareness about MS, but also TMS. I never want anyone diagnosed with MS to feel nor walk alone. I’m fundraising to advocate and spread MS awareness, help provide resources and information to support systems (friends, families, and communities), and to help my fellow MS patients with the vital necessities so we can live our lives the best as we can. I believe we are stronger in numbers so let’s join the fight and beat MS together!