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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

Dr. Vicki Wheelock is a neurologist and the director of the HDSA Center of Excellence at UC Davis Health. The mission of the HD clinic at UC Davis is to provide expert and compassionate care to people and families affected by HD,... more

Terry Tempkin, NP-C, MSN, is an Adult Nurse Practitioner who spent 18 years working with Huntington's disease families at the University of California Davis Health System. During her time there, she worked with the HD team to build... more

Please visit http://eurohuntington.org/ for more information.

For more information about KINECT-HD, please visit the HSG website at: https://huntingtonstudygroup.org/current-clinical-trials/kinect-hd/

https://www.rarediseaseday.org/ https://huntingtonsdiseasenews.com/2020/02/20/rare-disease-day-2020-recognized-around-the-world/ #whatmakesmerareHD

HDYO has a new Genetic Testing program! Please visit their website for more information: www.hdyo.org Matt Ellison's bio: "Hi! My role at HDYO includes developing all the educational project work we do for our website, including... more

Gene Veritas Rerun

Patty Romero-Mabry shares her HD experience as a caregiver for her husband and her son with JHD. For information on how you can help Patty and Bryan, please contact Lauren Holder at lauren@help4hd.org

Melissa (Dilley) Ryant has been a member of the Huntington's Disease Society of America's (HDSA) National Youth Alliance (NYA) since attending her first convention in 2013. From that point, Melissa volunteered to serve on the NYA... more

Melissa (Dilley) Ryant has been a member of the Huntington's Disease Society of America's (HDSA) National Youth Alliance (NYA) since attending her first convention in 2013. From that point, Melissa volunteered to serve on the NYA... more

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