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April 2018

The Huntington’s Disease Society of America’s Research Webinar

April 18, 2018 @ 12:00 pm - 1:00 pm
online

The HDSA Research Webinar This free webinar will present research from Dr. Jack Reidling. Dr. Reidling has been conducting experiments with stem cells by using them to replace the dead brain cells in mice with Huntington's disease. You can register for the webinar here: https://register.gotowebinar.com/register/8070448723031915521  

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June 2018

Huntington’s Disease Society of America – 33rd Annual HDSA Convention – Los Angeles

June 7, 2018 - June 9, 2018
Los Angeles Airport Marriott Hotel, 5855 W Century Blvd
Los Angeles, CA 90045 United States
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Huntington's Disease Society of America is hosting the 33rd Annual HDSA Convention in Los Angeles, California. The three day event will highlight educational workshops and forums, as well as a walk, gala and more. Ticket Fees: Early Bird Adult - $199 Early Bird Family - $175 (per person) To register and for additional pricing information please click here.

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June 2020

The Huntington’s Disease Society of America’s Annual Convention

June 4, 2020 - June 6, 2020
LA United States
$199

HDSA 35 New Orleans: The 35th Annual HDSA Convention June 4th-6th, 2020 The 35th annual convention is tailored for Huntington's disease patients and their families. Join the HDSA for three days of educational sessions, community building and sharing, and just plain fun. Attendees will have the opportunity to learn about the latest in Huntington's disease research and treatment and network with others that are affected by Huntington's. For registration information, click here. For information about the National Youth Alliance Scholarship…

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May 2022

Huntington’s Disease Society of America’s What Huntington’s Tells Us About Living Live Storytelling Showcase

May 11, 2022 @ 7:00 pm - 9:00 pm
Regent Theatre, 7 Medford St
Arlington, VA 02474 United States
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$25

What Huntington's Tells Us About Living Live Story Telling Showcase May 11, 2022 7:00 PM Join five people impacted by Huntington's disease as they share their inspiring stories about how the disease has shaped their lives and their perspectives. Storytellers include caregivers, medical professionals, and people testing positive for the gene mutation. To learn more, click here.

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