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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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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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PARTICIPATE IN AN HDSA EVENT NEAR YOU

HDSA has events across the country that you can participate in from the comfort and safety of your home. From the Virtual Team Hope Walks to scavenger hunts and wine tastings, there’s something for everyone to stay connected during these challenging times.

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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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This Week in HD Research

Dr. Leora Fox keeps you up-to-date on HDSA research activities, recently published work about Huntington’s disease, historical moments in HD research and more.

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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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