Landmark Legislation for the Parkinson’s Community!

We’re thrilled to share that on May 23, Congress passed the National Plan to End Parkinson’s Act, the first piece of legislation aimed at better diagnosing, treating, preventing and curing Parkinson’s disease.

The Need for a National Plan

The U.S. National Plan to End Parkinson’s Act aims to create a comprehensive strategy, integrating efforts across federal and state governments, private organizations, and research institutions. The primary objectives of this plan include:

Coordinating Research Efforts: By unifying the efforts of various research bodies, the plan aims to foster collaboration and data sharing, expediting the discovery of new treatments and potential cures.

Increasing Funding: Parkinson’s research has historically been underfunded compared to other neurological diseases. This plan proposes increased federal funding, encouraging private investment, and public donations to accelerate progress.

Raising Awareness: Public awareness campaigns are critical in educating the public about Parkinson’s disease, its symptoms, and the importance of early diagnosis and intervention.

Supporting Patients and Families: The plan emphasizes the need for better support systems for those affected by Parkinson’s, including access to care, mental health services and caregiver support.

For individuals living with Parkinson’s and their families, this Act represents hope above all!  With increased funding, coordinated research, and comprehensive support, the potential for significant advancements in treatment and care is huge.  It also symbolizes a national commitment to improving the lives of those affected by Parkinson’s disease and holds the promise of fast-tracking progress towards better treatment and ultimately, a cure.  The future is looking better and brighter everyday!

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