In Their Own Words
Nancy’s Story
Nancy describes her experience with diagnosis, The Elliot Lewis Center and seeking financial assistance from The ELC Foundation.
Read MorePam’s Story
When Pam’s strength and mobility declined, she sought help to regain her independence.
Read MoreLindsey’s Story
Lindsey’s MS story starts with an optic neuritis attack at 23 years old. She describes her journey over the last 15 years.
Read MoreVicki’s Story
Vicki shares her multiple sclerosis story, encouraging others to take an active role in their health care. Speak up. Ask questions. Seek support.
Read MoreSue’s Story
Sue shares her multiple sclerosis story of diagnosis, disbelief, anger and acceptance.
Read MoreHeather’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 that defines me.”
Read MoreJanet’s Story
MS helped Janet overcome self-imposed barriers as she stepped through the mirror to know her core values.
Read MoreBrad’s Story
Brad has found expression through art, drawing parallels in the wild uncertainty in the world, similar to the uncertainty of multiple sclerosis.
Read MoreMeg’s Story
Meg details how her MS diagnosis changed the trajectory of her life and how she learned to make lemonade out of lemons…
Read MoreSarah’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 her independence.
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