What do ALS and baseball have in common? At first glance, they may seem like two very different worlds. But if you dive deeper into history and the stories of perseverance, resilience, and hope, you'll find an unexpected and powerful connection.
In a brand-new episode of the Canadian Baseball Network podcast, our Executive Director and Founder, Cherrie, joins hosts Matt and Jackson to discuss this profound link. It’s a conversation that shines a light on not only the disease but also the enduring impact that one legendary baseball player had on the ALS community.
If you’ve heard of Lou Gehrig, the Iron Horse of baseball, you already know part of the story. But this podcast episode goes beyond just the history of Lou Gehrig's diagnosis of ALS – also known as Lou Gehrig's Disease. It delves into the ways that baseball, as a sport and a community, continues to play an important role in raising awareness and supporting the fight against this devastating disease.
Without giving away too much, we can promise you that this episode will make you think differently about both baseball and ALS. Whether you’re a lifelong fan of the game or just learning about ALS, this conversation will leave a lasting impression.
What You’ll Learn:
The history behind ALS Double Play’s connection to baseball, and the roots of the charity’s name.
Personal insights from Cherrie on how baseball can unite communities in the fight against ALS.
A look at ALS Double Play’s efforts to raise awareness for ALS, both on and off the field.
How you can get involved in the movement to strike out ALS.
Listen Now!
Curious to learn more? Don’t wait! Tune in to the full podcast to hear Cherrie’s conversation with Matt and Jackson. This episode is packed with heart, passion, and a call to action for everyone who wants to see a world without ALS.
👉 Take a listen here: bit.ly/24cbnALS
Together, we can keep swinging for the fences in the fight against ALS.
My husband was diagnosed August 2022. It was hard and I cry daily but not in front of him unless we cry together. He couldn’t find anything to give him happiness or hope. We have been focusing on our faith. He was only losing his voice before we made the decision to try different medications, which significantly enhanced his condition. He received the ALS/MND treatment for his ALS approximately four months ago; since then, he has stopped using a feeding tube, speech is getting better by the day, sleeps well, works out frequently. I’m surprised a lot of CALs, and their PALS haven’t heard of it, google uinehealthcentre.com. My husband has become very active