#LetsTalkAboutHD with Sarah Miller

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PASS THE HD PARITY ACT

We need your support to pass the HD Parity Act which will waive Medicare’s two-year waiting period for people with Huntington’s disease. It is time to take action because two years is too long!

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2020 YEAR IN REVIEW MAGAZINE

Despite the COVID-19 pandemic, the fight against Huntington’s disease did not stop. Take a look back at HDSA’s impact in the 2020 Year in Review Magazine.

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THE MARKER: HDSA’S 2020 RESEARCH REPORT

Updates on clinical trials, fellowships, conferences and the latest in HD research.

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COVID-19 & HD RESOURCES

We know the COVID-19 pandemic is a difficult time for all and may be particularly challenging for those living with or supporting someone with Huntington’s disease. HDSA is committed to sharing the latest updates and resources as we face this public health crisis together.

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FREE TELEHEALTH COUNSELING

Announcing free online therapy sessions for people affected by HD provided by HDSA & American Well®. HDSA-trained licensed social workers and psychologists will be available to HD families in all 50 states.

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VIRTUAL 36TH ANNUAL HDSA CONVENTION

Thank you to our incredible sponsors, exhibitors, partners and all our global attendees who helped make the Virtual 36th Annual HDSA Convention a massive success. All recorded sessions are now available for viewing!

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