Welcome to my fundraising page!

Did you know the lifetime risk fo developing ALS is just 1 in 300? There is no known cure for ALS, and once diagnosed patients typically live only three to five years. These are alarming facts about ALS, but we can help change the course of the disease and ensure that progress is made towards finding life-enhancing treatments and a cure.

The Les Turner ALS Foundation is here to care for those affected by the disease, answer their questions, and support them and their loved ones every step of their journey.

I am participating in the 2024 Bank of America Chicago Marathon as part of Team Race for ALS! In summer of 2023 one of my closest friend's father received the life shattering diagnosis of ALS. For the last ten years he has provided me with life advice, guidance, support, golfing tips, and numerous Chicago restaurant recommendations. After learning about his diagnosis, I knew I wanted to do something big in his honor, support him, and show how much he has positively impacted my life by running the Chicago Marathon!

I support the mission of the Les Turner ALS Foundation, and believe in providing the best possible care to people living with ALS and their families in the Chicagoland area. I am hopeful the funds we raise together will help advance the research and lead to a cure for ALS.

I'd greatly appreciate your support as I train for the marathon all in an effort to show support to Ken and the Jatczak family, and bring awareness to ALS. Please consider making a donation to help me reach my fundraising goal. If you're free on Sunday, October 13th, come cheer me on as I race throughout Chicago and cross the finish line at 26.2 miles!

All the best,

Alerie