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Huntington's disease as a family - Walters family

As part of HDYO's 'Talking about HD as a family' project, we interviewed the Walters family, who shared their experiences of talking about HD in their family. Thank you to Ellie, Flo, Meg and Ben for taking part. Four families bravely share their experiences of living with Juvenile Huntington's disease. We advise viewers to be aware that this topic may be upsetting, if you need support email us at [email protected]' I'f you'd like to learn more about HD and JHD, please visit www.HDYO.org. If you'd like to help support young people, like these in the video, impacted by HD, please consider making a donation to HDYO here: https://en.hdyo.org/eve/about/587

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