Bill 118 sres 224, also known as the 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 devastating neurodegenerative disease, which affects the 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 courage and resilience of those living with ALS and honors the memory of those who have lost their lives to the disease.
By designating May 2023 as "ALS Awareness Month," the resolution seeks to bring attention to the challenges faced by ALS patients and their caregivers, as well as the urgent need for a cure. It calls on the government, healthcare providers, and the public to work together to improve the quality of life for ALS patients and ultimately find a cure for this devastating disease.
Overall, Bill 118 sres 224 aims to raise awareness, promote research, and support individuals and families affected by ALS, with the ultimate goal of finding a cure and improving the lives of those living with the disease.