Patient Advocacy :: Amelia Davis

When I was diagnosed with multiple sclerosis I felt frightened and alone. No one should have to feel that way. Now, through speaking out at Direct To Patient programs, through my photography, and as being President of MSFriends, I try to help the newly diagnosed know that they are not alone, and that they can take control of their disease and not let it control them. Patients helping patients is a way of helping people feel empowered and take an active role in the outcome of their lives.

Kaley & Rona, Photo from My Story
Kaley is the founder of Youth Against MS