August 9th, 2023
Robert Cochrane
Parkinson’s disease (PD) is the thing that goes bump in the night. I can’t always see its physical effects, but I can always feel it there, lurking. It’s also the fastest-growing neurological disease in the world and, according to the authors of Ending Parkinson’s Disease, a pandemic. For those who know me, you know that […]
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July 18th, 2023
Robert Cochrane
It’s time we got serious about Ending Parkinson’s disease – the book and the movement. My latest writing class with PD participants, “Day One: The Parkinson’s Prison and the Hero’s Journey to Escape” is 10 weeks into their 16-week journey and they are producing fantastic work that demands to be seen. Similar to the previous […]
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July 9th, 2023
Robert Cochrane
Thousands of researchers, clinicians, people with and affected by PD descended upon Barcelona last week for the sixth annual World Parkinson’s Congress (WPC). It was my first and I was thrilled to take part. I’ll give a broad overview here – please know I could fill pages with more details as it was a deeply […]
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June 30th, 2023
Robert Cochrane
Telling a sad sack story about Parkinson’s disease (PD) is boring. That’s what Michael J. Fox tells us in the first ten minutes of his new biographical documentary, Still (available on Apple TV+). He’s not only right, he’s showing all of us how to change the trajectory of PD: by telling our own heroic journeys, […]
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April 28th, 2023
Robert Cochrane
This is a blended letter written from Susan Scarlett, beginning at the end of the 2021 Day One Superheroes program, and revised before the start of the 2023 Day One Parkinson’s Prison program. For more information on the Day One program, please visit: https://www.yesandexercise.org/about-3 Dear Day One PD Superheroes and fellow Parkinson’s Prisoners, I have […]
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February 28th, 2023
Robert Cochrane
Written by YAX’s own First Follower, Susan Scarlett Prior to my diagnosis of Parkinson’s, I began to notice my handwriting shrinking. After my diagnosis, I learned that this phenomenon has a name – micrographia – and it is a very normal part of the Parkinson’s experience. In the years since then, my handwriting has become […]
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February 23rd, 2023
Robert Cochrane
Traveling is not easy for my dad, a 78-year-old man who was diagnosed with Parkinson’s disease (PD) in 2001. At the same time, him missing out or feeling that he is being left out, is something I’m so sensitive to that I’m willing to put in the effort to make sure he gets to participate […]
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February 2nd, 2023
Robert Cochrane
Our current medical system is brilliant at acute and emergency care. We have fantastic and dedicated practitioners, surgeons and specialists, amazing drugs, tools, and even precise robots which can treat, extract and connect us to technology in ways that save lives and give the opportunity for a greater quality of life. Yes, that’s all true […]
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January 30th, 2023
Robert Cochrane
Here’s a snippet of our interview with Cole Galloway, PhD. His research Research focuses on physical rehabilitation for children. He is founder of the Go Baby Go program, which helps children and adults with physical and developmental disabilities move and explore the world. ROBERT: Hi Cole, how are you? COLE: Hey fellas and ladies. I’m […]
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January 25th, 2023
Robert Cochrane
The following is the opening transcript from an interview with an awesomely inspiring Run Disney enthusiast who has been making and wearing amazing Disney-themed costumes on the courses for over ten years. For the whole episode, please click this link. Robert: Tell me about your history with run Disney. Cindy: For those of you who […]
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