If you’re familiar with ALS, you know it’s a progressive neurological disease that gradually destroys the motor neurons responsible for movement, eventually leading to paralysis. In June 2025, I was diagnosed with a slower-progressing form of ALS. While it advances more slowly than classic ALS, it has already taken away the use of my arms and hands, and is now beginning to affect my legs.
For many years, running this website has been far more than a hobby—it’s been a passion, a creative outlet, and a way to connect with people from coast to coast to coast. As ALS has changed nearly every aspect of my daily life, maintaining the site has become one of the few meaningful activities I can still do. It gives me a sense of purpose, accomplishment, and connection that is difficult to put into words.
Despite the physical challenges, I remain committed to keeping the website updated, useful, and available to the community that has supported it over the years. However, the reality is that the costs of hosting, security, software, and ongoing maintenance significantly exceed the income generated through advertising and affiliate links.
As my condition progresses, I am also facing increasing personal and accessibility-related expenses. To help me continue operating the website and remain in my home for as long as possible, a close friend has kindly organized a GoFundMe campaign on my behalf.
If this website has ever helped you, taught you something, saved you time, or simply provided value, I would be incredibly grateful if you would consider supporting the campaign. Whether it’s a donation, sharing the fundraiser with others, or simply spreading the word, every act of support makes a meaningful difference.
Thank you for being part of this journey. Your kindness, encouragement, and generosity help me continue doing something I love while navigating the challenges that lie ahead.
