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How 'Huntington's Disease Society of America' Funds Treatment, Research, Community, and Advocation For Those With HD

Author
Nicholas Hill
Published
Wed 27 Jul 2022
Episode Link
None

Today we interview Louise Vetter, President and CEO of Huntington's Disease Society of America, about the work they do for those impacted by Huntington’s Disease. We’ll discuss the complex symptoms and unique challenges surrounding this disease, the ways in which HDSA helps patients, their families, and caregivers, and the research grants and legislation HDSA is supporting to bring progress and relief. 

To support HDSA and discover more ways to help, visit: 
https://hdsa.org/

To learn more about the show, view transcripts, and more visit:
https://www.actsofimpact.com

Special thanks to Louise and the HDSA team. Music by Alex Grohls.

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