Louisiana Senate Bill SR116

Louisiana 2024 Regular Session

• Introduced: 5/21/24
• Passed: 5/22/24

Caption

Designates the month of May as ALS Awareness Month in Louisiana.

Impact

The recognition of May as ALS Awareness Month has the potential to enhance public understanding of the disease, leading to more support for research funding and advocacy for individuals living with ALS. The resolution calls attention to the challenges faced by patients and their families, including the need for new therapies and assistive technologies. By highlighting the role of organizations like the ALS Association, which invests heavily in ALS research, the resolution seeks to mobilize community support and funding for better healthcare solutions.

Summary

Senate Resolution 116 (SR116) designates the month of May as ALS Awareness Month in Louisiana. This resolution aims to raise awareness about Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease, and to acknowledge the impact it has on individuals, families, and communities. The resolution emphasizes that ALS is a progressive and fatal neurodegenerative disease, with no known cure, significantly affecting the quality of life for those diagnosed with it. Every 90 minutes, someone is diagnosed with ALS, highlighting the urgency of increased public awareness and support for research funding.

Sentiment

The sentiment surrounding SR116 is predominantly positive, as it reflects a collective commitment to raising awareness and supporting those affected by ALS. Legislators and advocacy groups likely view the designation of ALS Awareness Month as a significant step toward fostering community solidarity and improving the quality of life for people living with ALS. There is also a sense of urgency due to the declining survival rates for ALS patients and the need for continued research.

Contention

While SR116 is generally well-received, there may be underlying concerns about the adequacy of funding for ALS research and treatments. Advocates worry that despite increased awareness, tangible support and funding may still fall short of what is necessary to address the needs of ALS patients effectively. The resolution aims to bridge this gap by encouraging greater involvement from the public and state officials alike to address these important health issues.