We are seeking Phi Delta Theta and Live Like Lou volunteers in the DC/MD/VA area to take photographs of a meaningful flag display at the National Mall for people living with and affected by ALS (Amyotrophic Lateral Sclerosis), also known as Lou Gehrig’s Disease.

Make a real difference for people and their families living with ALS by coming out to the National Mall on Wednesday, May 29 from 1 PM to 6 PM (or until the project is completed) to help take pictures of 6,000 flags that symbolize the number of people diagnosed with ALS this year. Flags are personalized for people living with and lost to ALS as well as ALS gene carriers. Photographs will be downloaded and shared all over the country.

Volunteers should meet at the National Mall between Washington Monument and 14th St NW. Metro stops near the installation are Smithsonian and Archives/Navy Memorial/Penn Quarter.

Volunteer Registration
https://forms.office.com/r/w424hwujPf

Questions? Please email Deb Paust, Community Organizing Associate at I AM ALS, at deb@iamals.org or Emily Johnson, Communications and Operations Associate, at emily@iamals.org.

Phi Delta Theta and Live Like Lou are proud to partner with I AM ALS in support of their DC ALS Awareness Event 2024.

About Live Like Lou
Named in honor of MLB Hall of Famer Lou Gehrig, a member of Phi Delta Theta Fraternity, Live Like Lou supports ALS families, funds emerging researchers seeking meaningful treatments and cures for ALS, and helps generate awareness of Lou Gehrig’s disease. Learn more at https://www.livelikelou.org.