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You are here: Home / News / Q&A About the National Plan to End Parkinson’s Act – Webinar on June 17, 12pm

Q&A About the National Plan to End Parkinson’s Act – Webinar on June 17, 12pm

June 10, 2024 By Stanford Parkinson's Community Help

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The National Plan to End Parkinson’s Act is becoming federal law! Join a special live broadcast on June 17 at 12:00 pm — Big Step for Parkinson’s: Q&A About the National Plan to End Parkinson’s Act, hosted by the American Parkinson Disease Association (APDA) to learn what this new law really means.

The National Plan to End Parkinson’s is is the first-ever federal legislation dedicated to curing and preventing Parkinson’s disease (PD) and striving for quality care for those impacted by this chronic and progressive neurologic disease.

On Monday APDA President and CEO, Leslie A. Chambers will be joined by the Senior Vice President of Public Policy at the Michael J. Fox Foundation, Ted Thompson. Ted led the advocacy team that was instrumental in getting the bill passed.

Register now to join Leslie and Ted as they discuss how this new law will impact people with PD today, and in the future, provide the latest updates on the status of the law, explain why it is so important, and answer many of the big questions you may have, including:

  • What happens next with this new law?
  • How can people get involved?
  • When can we expect to see progress?
  • And so much more!

Filed Under: News, Webinars - Announcements & Notes

Stanford Parkinson’s Community Outreach provides vital resources and support to individuals living with Parkinson’s disease (PD), caregivers, family members, and friends. We curate a comprehensive list of PD-related webinars and virtual meetings, sharing insightful summaries through our blog and dedicated email lists. Whether you seek online support groups, educational webinars, or access to helpful blogs and podcasts, we are here to empower you with the knowledge and connection you need on your Parkinson’s journey.

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