Bill 118 S.Res. 239, also known as a resolution designating May 2023 as "ALS Awareness Month," was introduced in the US Congress with the aim of raising awareness about Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. The resolution highlights the importance of educating the public about this debilitating neurodegenerative disease, which affects nerve cells in the brain and spinal cord, leading to muscle weakness and paralysis.
The resolution emphasizes the need for increased research funding and support for individuals and families affected by ALS. It recognizes the challenges faced by those living with ALS and their caregivers, as well as the importance of early detection and access to quality healthcare services.
By designating May 2023 as "ALS Awareness Month," the resolution seeks to bring attention to the impact of ALS on individuals and communities across the country. It encourages individuals, organizations, and government agencies to participate in activities and events that promote awareness and support for those affected by ALS.
Overall, Bill 118 S.Res. 239 aims to raise awareness about ALS, promote research and support for individuals living with the disease, and encourage greater understanding and compassion for those affected by this devastating condition.