MS became a big part of my life when I was 19. I found that I could barely stand near the end of my shifts at my new retail job. When I was newly diagnosed it was devastating but it was barely affecting my life so I kept moving forward, going to college and working. I use a cane now because I trip/fall frequently and I have tried different types of treatments. I hope to be cured from this or even gain my walking ability back and hope to emotionally help those in need. I know how it feels to not be heard or understood, MS is a hard concept for a lot of people to grasp and I hope to bridge that gap.