in their own words
in their own words
Heather’s Story
Heather's story emphasizes "You are not alone. ELC makes MS just a thing I take care of on the side and not a disability ...
Janet’s Story
MS helped Janet overcome self-imposed barriers as she stepped through the mirror to know her core values. Spring 2022: Typically at this time of ...
Brad’s Story
Brad has found expression through art, drawing parallels in the wild uncertainty in the world, similar to the uncertainty of multiple sclerosis. I have ...
Meg’s Story
Meg details how her MS diagnosis changed the trajectory of her life and how she learned to make lemonade out of lemons... I was ...
Sarah’s Story
Sarah talks about her experience with driving & multiple sclerosis. Read about the modifications Sarah made to her car to allow her to keep ...
Cynthia’s Story
Cynthia shares her story of trying to keep a positive attitude and how her support team at The Elliot Lewis Center helps her physical ...
Bernardo’s Story
Hi. My name is Bernardo, and I’ve been living with MS since 2010. I was a third-year law student when the double vision started. ...
Dan’s Story
About 16 years ago when my daughter was 7 months old, I turned around to watch her crawling, and noticed I had double vision. ...
Shan’s Story
Every journey with MS is unique. That, combined with how every life is unique, makes it almost impossible for any one person to relate ...
Carrie’s Story
Carrie has been part of the ELC family for four years. A self-described extrovert, Carrie holds a PhD in psychology and currently works as ...
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