A resolution designating May 2024 as "ALS Awareness Month".

Bill 118 S.Res. 713, also known as a resolution designating May 2024 as "ALS Awareness Month," was introduced in the United States Senate. The purpose of this resolution is to bring attention to amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, and raise awareness about the impact it has on individuals and their families.

ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord, leading to muscle weakness and paralysis. There is currently no cure for ALS, and the average life expectancy after diagnosis is 2-5 years.

The resolution recognizes the importance of increasing public awareness about ALS, supporting research efforts to find a cure, and providing support for individuals and families affected by the disease. By designating May 2024 as "ALS Awareness Month," the resolution aims to educate the public about the challenges faced by those living with ALS and encourage greater support for research and advocacy efforts. Overall, Bill 118 S.Res. 713 seeks to raise awareness about ALS and promote efforts to improve the lives of individuals and families affected by this devastating disease. It highlights the need for continued research, support, and advocacy to find a cure for ALS and improve the quality of life for those living with the disease.