in their own words
in their own words
Connie’s Story
52 Years of Living with MS: My Journey My MS story began in 1972 when I was a sophomore in college. During finals week ...
Katy’s Story
Katy representing ELC! Katy learned about the Infusion Access Foundation's Champions Weekend through The Elliot Lewis Center. Katy was inspired and submitted an application, ...
Sue P’s Story
While navigating her diagnosis with multiple sclerosis, Sue aspires to uplift and inspire other patients through her community activities and involvement with the National ...
Lisa’s Story
Lisa talks about finding community through the B.Fit! program at The Boston Home. In 1984, I was diagnosed with RRMS. I was a very ...
Noelle’s Story
Noelle’s resilience and positive energy empower her to "Rock It"! I was seventeen when I had my first MS symptoms. I was at boarding ...
Dawn’s Story
Dawn describes how running has changed her life. Her passion and determination led her to found a charity to support patients with chronic disease. ...
Tammie’s Story
Tammie tells her story of working with NEADS to match with a service dog. My name is Tammie DeCroteau and I was diagnosed with ...
Dana’s Story
Dana tells her story of how and why she stopped driving, and the challenging questions she addressed in making that decision. Could she give ...
Nancy’s Story
Nancy describes her experience with diagnosis, The Elliot Lewis Center and seeking financial assistance from The ELC Foundation. Back in 2018, I noticed that ...
Pam’s Story
When Pam's strength and mobility declined, she sought help to regain her independence. I was diagnosed with PPMS in 2017. It was a ...