I'm participating in ALS United Greater New York's Walk ALS to raise funds that will support individuals and families affected by ALS.

This cause is personal to me. Three years ago this August, I lost my mom to a courageous battle with ALS. Watching her face this disease with such strength and grace is something I carry with me every day, and it's why I'm walking — to honor her memory and to help other families who are going through what mine did.

My mom, Lynn, was an incredible nurse, and in her honor, my family created the Lynn M. McCormack Memorial Foundation. The foundation awards scholarships to graduating high school students pursuing a career in nursing, so that we can keep investing in the next generation of nurses the same way she invested in her patients throughout her career. You can learn more here www lynnmccormackfoundation org. 

Amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its ability to walk, speak, swallow and breathe. The life expectancy of a person with ALS averages 2 to 5 years from the time of diagnosis. ALS can strike anyone regardless of age, gender, nationality, or ethnicity, although it is primarily an adult-onset disease. Currently there is no known cause or cure.

Being a part of ALS United Greater New York's Walk ALS is the number one way to unite and fundraise for those living with ALS. Please consider supporting my efforts by donating through my fundraising page.

Your donation today will help fund resources and services to the local ALS community, help find new ALS treatments, and move us closer to a world without the disease.

Please feel free to send this page to any friend or family member who might be interested in donating!

Thank you, and thank you for being part of my mom's legacy.

- Ashley Lynn McCormack