The ALS Better Care Act, also known as Bill 118 s 3258, is a piece of legislation currently being considered by the United States Congress. The bill aims to improve care and support for individuals suffering from Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease.
The key provisions of the ALS Better Care Act include:
1. Establishing a national ALS registry to track the prevalence and incidence of the disease, as well as to improve research and treatment options.
2. Providing funding for research into the causes and potential cures for ALS, with a focus on developing new therapies and treatments.
3. Improving access to care and support services for individuals with ALS, including palliative care, home health services, and assistive technology.
4. Enhancing education and training for healthcare providers to better diagnose and manage ALS patients.
5. Increasing awareness and understanding of ALS within the medical community and the general public.
Overall, the ALS Better Care Act seeks to address the unique challenges faced by individuals with ALS and improve their quality of life through better care, support, and research efforts. It is currently under review in Congress and has garnered bipartisan support for its efforts to combat this devastating disease.