Summary of the Bill

House Resolution 1136 proposes the designation of April 2024 as "Parkinson's Awareness Month." It acknowledges the widespread impact of Parkinson's disease, affecting over a million Americans, with nearly 90,000 new diagnoses annually. This initiative seeks to promote further research and education, while also highlighting the contributions of those living with the disease and participating in clinical trials. The resolution aims to commend and support the ongoing efforts of organizations and individuals dedicated to enhancing the quality of life for those impacted by Parkinson's disease.

Significant Issues

The resolution raises awareness of several key issues associated with Parkinson's disease. These issues include the increasing prevalence and substantial economic burden of the disease, which is expected to nearly double by 2037. The resolution underlines the importance of addressing the symptoms patients face, such as motor and cognitive challenges, and the significant role family caregivers play in managing these conditions. It stresses the necessity for increased research, education, and community support services to find better treatments and, ultimately, a cure for Parkinson’s.

Impact on the Public

The broad intent of this resolution is to foster greater awareness and understanding of Parkinson’s disease among the general public. By designating a specific month for awareness, it encourages public engagement in education and advocacy efforts surrounding the disease. It invites increased public participation in supporting those affected by Parkinson’s and underscores the importance of advancing scientific research and clinical trials. The heightened awareness could potentially lead to more community support initiatives and increased funding for research, which may benefit all individuals and families dealing with the disease.

Impact on Specific Stakeholders

For individuals living with Parkinson's disease and their families, the designation of a Parkinson's Awareness Month provides recognition and validation of their challenges. It highlights the need for support systems and could spur improvements in services and resources available to them. Researchers and healthcare professionals might find renewed interest and investment in their work, possibly accelerating advancements in treatments and care strategies. Non-profit organizations and advocacy groups dedicated to Parkinson's will likely gain more visibility, which could enhance their efforts in fundraising and expanding their outreach programs. However, the resolution itself does not propose specific funding or policy changes, which may limit its impact without further legislative action or resource allocation.