This series features essays by Dr. Kenneth Serbin, Professor of History, originally posted on his blog, At Risk for Huntington's Disease."

Huntington's Disease (HD) is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment.

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Blog Posts from 2017

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Banning college football: an urgent objective for brain health advocates, Kenneth P. Serbin

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Passing on the Huntington’s disease advocacy baton to the next generation, Kenneth P. Serbin

Blog Posts from 2016

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This Thanksgiving, let’s show gratitude for disease researchers and drug hunters, Kenneth P. Serbin

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‘Crying a few million tears’ for the fallen victims of Huntington's disease, Kenneth P. Serbin

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Ionis Phase I Huntington’s disease trial at halfway mark: 'No surprises so far' means good news, Kenneth P. Serbin

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Dreams for a better future: an opportunity we Huntington's disease people and our families are denied, Kenneth P. Serbin

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Upbeat Huntington’s disease film, featuring undaunted family, aims for 10 million views, Kenneth P. Serbin

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A family united against Huntington’s disease, Kenneth P. Serbin

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From sheepish to self-assured in the fight against Huntington's disease, Kenneth P. Serbin

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Just living life: a focus on what matters most in coping with the risk of Huntington's disease, Kenneth P. Serbin

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Billboards: an old – but also new – way of projecting the Huntington's cause, Kenneth P. Serbin

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Chief Huntington’s disease drug hunter: ‘every confidence first treatments' in the works, Kenneth P. Serbin

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The little things that are really big: caregiving in families with Huntington's disease, Kenneth P. Serbin

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Defeating Huntington’s disease starts with taking care of yourself and joining Enroll-HD, Kenneth P. Serbin

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A key Huntington’s disease trial remedy gets Orphan Drug Designation, as yet another young life is cut short, Kenneth P. Serbin

Blog Posts from 2015

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‘Concussion’: advocating for the truth about brain diseases, Kenneth P. Serbin

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‘Twas the morning after Christmas – and Huntington's disease hit us like a ton of bricks, Kenneth P. Serbin

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How to make law enforcement a friend – not a foe – of people with Huntington's disease (and other disabilities), Kenneth P. Serbin

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With more Huntington’s disease clinical trials, volunteers need help with comparison shopping, Kenneth P. Serbin

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Might I finally take part in a Huntington’s disease clinical trials? An update on the latest research, Kenneth P. Serbin

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Huntington’s disease patients get first dosing in historic Isis Pharmaceuticals' gene-silencing drug trial, Kenneth P. Serbin

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At-risk Angels pitcher Joe Smith at Huntington’s fundraiser: 'I'd give every dime I have for a cure', Kenneth P. Serbin

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At key FDA meeting, Huntington's disease community insists on faster search for treatments, Kenneth P. Serbin

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As he lay dying: FDA and Huntington’s disease families meet to ponder potential treatments, Kenneth P. Serbin

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New film unmasks the raw reality of Huntington’s disease, Kenneth P. Serbin