The Senate Resolution designates the month of May as ALS Awareness Month in Louisiana, highlighting the severe impact of Amyotrophic Lateral Sclerosis (ALS), commonly known as Lou Gehrig's disease. ALS is a progressive neurodegenerative condition that leads to the loss of muscle control, ultimately affecting a person's ability to walk, talk, eat, and breathe. The resolution emphasizes the urgency of raising awareness about ALS, noting that someone is diagnosed with the disease every 90 minutes, and that there is currently no cure. It also points out that military veterans are at a higher risk of developing ALS and underscores the importance of access to new therapies and assistive technologies for those living with the disease.

The resolution calls for increased public awareness and support for ALS research, particularly in light of the upcoming 10th anniversary of the ALS Ice Bucket Challenge, which significantly contributed to funding for ALS research. The ALS Association, a major philanthropic supporter of ALS research, has invested over $154 million in various projects aimed at finding a cure and improving the quality of life for those affected. By designating May as ALS Awareness Month, the resolution encourages all Louisianians to advocate for increased funding and to stand in solidarity with individuals and families impacted by this debilitating disease.