As we kick off ALS Awareness Month I reflect on my journey since receiving a diagnosis in 2023. For those who may not be familiar, ALS, Amyotrophic Lateral Sclerosis, is a chronic neurodegenerative disease that causes progressive weakness of the muscles, affecting movement, speech, swallowing, and breathing. With only about 20,000 individuals affected, the chance of facing this challenge is rare, about 1 in 400. While there's no cure, there are two drug regimens available that slow down the progression. These numbers highlight the importance of spreading awareness and offering support to those impacted by ALS.

Organizations like Team Gleason have been instrumental, offering invaluable support through loaner equipment programs, and a variety of support services that have truly made a difference to me in my journey with ALS.

As I dive into fundraising efforts this month, I'm filled with a sense of purpose and optimism. This journey has taught me so much, and I'm determined to spread awareness and make a difference. Amidst the facts about ALS lies a spark of hope. Your generous support can help transform this hope into impactful change. Together, let's shine a light on ALS and work toward a future without it.

No White Flags!