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It was hard to miss Alan Alda’s announcement this week on CBS This Morning that the legendary actor had been diagnosed with Parkinson’s disease more than three years ago. Alda, 82, said one of the reasons he was speaking out was to offer a message of hope to people who are living with the disease: “In the very beginning, to be immobilized by fear and think the worst thing has happened to you – it hasn’t happened to you. You still have things you can do. I’m taking boxing lessons three times a week. I do singles tennis a couple of times a week. I march to Sousa music because marching to music is good for Parkinson’s.”
Through the years, our Dana Foundation publications have often focused on both Parkinson’s disease and Alda’s passion to better communicate science to the public, which is part of our mission as well.
In 2015, about the same time that Alda learned he had Parkinson’s, I wrote “Alda Crushes It,” a blog on Alda’s lecture at Columbia University, entitled “Getting Behind a Blind Date with Science.” In this captivating lecture, co-sponsored by Dana and the Kavli Foundation, he talked about why he had co-founded his own center for science communication at Stony Brook University and how he had been inspired by his time as host of Scientific American Frontiers, a PBS program that explored any number of topics. He was engaging, insightful, and his enthusiasm was contagious.
A year later the publication I edit, Cerebrum, reviewed Alda’s new book If I Understood You, Would I Have This Look on My Face. We asked Eric Chudler, a neuroscientist at the University of Washington and the executive director of the Center for Sensorimotor Neural Engineering in Seattle, to tell us what he thought. Chudler wrote: “With humor and a clear, concise, and never stilted writing style, Alda takes readers on his journey to help experts convey neuroscience and other complex scientific topics to a variety of audiences.”
Last year Cerebrum published “Gut Feelings on Parkinson’s and Depression,” an article by Ted Dinan and John Cryan, researchers at the University of Cork in Ireland, that focused on microbiota’s emerging role in trying to solve the puzzle that could lead to treatment. We also published “A Smell Test for Parkinson’s,” an article about the growing role of olfactory in diagnosing the disease.
Alda told CBS that one of the reasons he decided to reveal that he was living with Parkinson’s was that he had been on television a lot in the last few weeks talking about Clear + Vivid, his new podcast. He noticed watching himself that his thumb was twitching and felt that “it’s probably only a matter of time before somebody does a story about this from a sad point of view, but that’s not where I am.”
All of us at the Dana Foundation are rooting hard for Alda—and know that he will continue to serve as a role model to others with Parkinson’s or any other potentially debilitating neurological disorder.