$39,247 / $400,000
Thanks for visiting my fundraising page!
TOM
I am playing in the event for my grandfather, Jim Morgan. Three years ago, my grandfather was diagnosed with ALS and I’ve seen firsthand the effects of the disease. While it may have slowed him down physically, my grandfather continues to maintain the same vibrant, outgoing personality I’ve always known and admired as he battles this disease. He continues to spend his days laughing with friends and family telling stories, most of which have become more and more fictional over the years. However, it wouldn’t be a proper Jim Morgan story without a good embellishment or two.
My grandfather has always told me the most important lesson in life is building and maintaining relationships, which he credits to all his success. As someone who was in the insurance business for nearly 40 years, he exemplified just that. There was never a place we could go together where he wouldn’t run into someone he knew or at the very least, someone who knew him. I can’t even begin to count how many people I’ve met over the years who have told me all the incredible things he had done for them.
My grandfather was the one who introduced me to the game and I cherish the memories of hitting balls off the mats at our lake house in Deep Creek, Maryland as a young boy. Once I learned about this event from Alex and my uncle, Joe, I couldn’t think of a better way to pay tribute to my grandfather and so many others affected by ALS.
JOE
I’m playing in honor of my dad, Jim Morgan, who has touched so many lives over his 86 remarkable years. He’s built an incredible legacy—first in the insurance business, where he formed countless friendships, and later through his generosity and tireless support for the dyslexic community. Jim’s love for golf is second to none: since the age of 12, he’s played hundreds of rounds each year, enjoyed the game on courses all over the globe, and created a lifetime of memories with friends and family.
Three years ago, my dad was diagnosed with ALS, a truly terrible disease that has slowly robbed him of physical abilities. It’s heartbreaking to watch someone so vibrant and full of life have to battle such a relentless illness. Yet, even as ALS has brought new challenges, his humor, signature storytelling, and gift for building relationships remain unchanged. He’s handled it all with a courage and grace that inspire everyone around him. As his son, I’m grateful for the lessons he’s taught me, the memories we’ve shared, and the example he’s set every step of the way. More than anything, I hope that through awareness and events like this, we can help find a cure for this devastating disease.