The Mooresville Board of Commissioners took a significant step towards raising awareness for amyotrophic lateral sclerosis (ALS) during their meeting on May 19, 2025, by officially proclaiming May as ALS Awareness Month. This proclamation highlights the urgent need for public understanding and support for those affected by this progressive and fatal neurodegenerative disease, commonly known as Lou Gehrig's disease.

Commissioner Qualls presented the proclamation to Dawn Swink, a representative from the ALS community, emphasizing the importance of awareness and advocacy. The proclamation outlines the devastating effects of ALS, which gradually robs individuals of their ability to walk, talk, eat, and breathe. It notes that every 90 minutes, someone in the United States is diagnosed with ALS, and another person succumbs to the disease.

The resolution calls for increased public awareness of the challenges faced by ALS patients and their families, as well as the critical need for access to new therapies and assistive technologies. It also underscores the role of clinical trials in developing new treatments and improving the quality of life for those living with ALS.

The ALS Association, recognized as a leading philanthropic organization in ALS research, has committed over $154 million to support numerous projects aimed at finding a cure. The proclamation encourages all Americans to advocate for increased funding for ALS research and to stand in solidarity with those impacted by this relentless disease.

As Mooresville observes ALS Awareness Month, the community is urged to engage in efforts that support research and raise awareness, reinforcing the commitment to making ALS a livable disease until a cure is found.