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Help4HD

Help 4 HD Live!

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Welcome to Help 4 HD Live! We are proud to broadcast credible information and education to the Huntington's disease community on a weekly basis. Help 4 HD Live! broadcasts every week providing vital information and inspiration to our Huntington's community. We have been blessed to interview many of our JHD/HD researchers, medical professionals, care providers and the pharmaceutical industry for six years. Join our Hosts, Katie Jackson each week for incredible programming and don’t forget to share this channel with your colleagues, family and friends. **Help 4 HD Live! is made possible through an education grant from Teva Pharmaceuticals and the Griffin Foundation. Thanks for tuning in! Help 4 HD International Inc. **Please consult with you own physician for advice about any medical recommendation.

On-Demand Episodes

Angie Rowe joins the Global Genes team as Chief Operating Officer. She has over 17 years experience in executive management of LLCs and non-profits. She most recently spent the past 8 years managing and directing various aspects of... more
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Help4HD

Tune in to hear Katrina Hamel talk about placing our loved ones with HD. We hear over and over about the challenges our families face when it comes to placing their loved ones with HD. Katrina has worked in hospice care for over 15... more
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We are excited to have Gia Mannone on the show with us to talk about her advocacy projects she is working on to spread awareness about HD. Gia has done some very creative and successful awareness campaigns on social... more
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Tune in to hear Katie Jackson and Katrina Hamel discuss all that Help 4 HD International did for Huntington's Awareness Month
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Help4HD

About HSG The Huntington Study Group (HSG), which was formed in 1993, is the world's first HD cooperative therapeutic research organization. Today, HSG is a world leader in facilitating high quality clinical research trials and studies... more
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Lauren Steffan will be on with us to talk about all that she is doing to advocate for our HD community when it comes to research and care.
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Seth found out as a 15-year-old that his mom had a rare, neurological, genetic disease known as Huntington's Disease (HD). HD is like having symptoms of ALS, Alzheimer's, and Parkinson's all at once, and there currently is no cure. Five... more
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Join us as founder and creator, Casey Herrington discusses the Huntington's Disease Global Ecosystem Map (HD GEM) Project. HD GEM Project's mission is to further engage with the "silent" 70% of the HD community by helping those... more
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Join our host, as Ginnievive Patch discusses her recent article in The Huntington's Post about Survivor's Guilt. It is very common for family members that are HD negative to feel guilty about their results.
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Tune in to hear Cossetta Stroud talk about her organization Cozie Care and an event they are hosting in Southern California.
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