Welcome to my personal fundraising page!
On October 13th, Jimmy and I are running the 2024 Chicago Marathon as part of TeamALS. This organization does such important work. Funding provides for support and resources for patients and their families including various therapies, in-home care, adaptive equipment, support groups and more. We need your support to make our efforts really matter!
ALS, also known as Lou Gehrig’s Disease, is a deadly illness with no known cause or cure. It affects the motor neurons in a person's brain and spinal cord. When the motor neurons die, the muscles waste away. Gradually, a person is robbed of the ability to walk, speak, eat, and eventually breathe. 85% of patients live less than 5 years after diagnosis.
My Aunt Jane endured so much during her battle with ALS; she lived with such grace through the very end. My dear friend Brandon was diagnosed 4.5 years ago at the age of 35. Brandon and his wife visited Sun Valley in the fall of ‘22. With the help of so many generous local friends and businesses, we put together an enjoyable, memorable trip. Here is an interview from early-on in Brandon's journey with ALS: https://www.instagram.com/tv/CaC9LQCpFhf/
This is why we're running – for those who can’t. My personal fundraising goal is $1,250 and I hope you’ll help me reach it. By making a one-time, tax-deductible donation, you can truly make a difference in the fight against ALS.
Any amount you feel comfortable giving is deeply appreciated. Every dime makes a difference! With your support, we can make a positive impact today on the lives of those living with Lou Gehrig’s Disease.
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