by Suzanne Alford | Nov 21, 2024 | Advocacy, Latest News, Technology
Technology is advancing at an unprecedented pace, and its impact on communities like those living with ALS is monumental. SpeakFaster is a transformative example of using advancements in machine learning and artificial intelligence to make a tangible difference in...
by Kacie Banegas | Apr 2, 2024 | Advocacy, Blog, Latest News, Raising Awareness
March 2024by Katherine O’Hagan, Team Gleason, Director of Development This is a day that I’ll hold close to my heart, and one that so clearly reaffirms my “why” in leading development for Team Gleason Foundation. These photos below are from the Rupesh Kotiya... by Suzanne Alford | Mar 4, 2024 | Advocacy, Latest News, Resources
Welcome to Team Gleason’s National Amyotrophic Lateral Sclerosis (ALS) Registry Information Page! The National ALS Registry is a crucial initiative designed to empower individuals living with Amyotrophic Lateral Sclerosis (ALS) to actively participate in...
by Kacie Banegas | Feb 1, 2023 | Advocacy, Fundraising/Events, Raising Awareness
January 2023 Team Gleason would like to extend a thank you to the BPO Elks 599 for their recent donation. Sarah Campbell, who lives with ALS, and her husband, Lionel, have been members of the lodge, located in Hattiesburg, MS for over 30 years. “The lodge...
by Kacie Banegas | Oct 17, 2022 | Advocacy, Fundraising/Events, Raising Awareness
October 2022by Joy F. A couple of weeks ago, Caleb reminded us he needed 2 service hours for school each quarter. With the first quarter coming to an end, he asked our neighbors how he could help them. If you’ve ever met Stephanie and Jay, you’d want to go...
by Suzanne Alford | Jan 5, 2021 | Latest News, Advocacy, Blog, Raising Awareness
Ten years ago I was diagnosed with ALS. Right at this moment, I feel a profound sense of gratitude, meaning, and responsibility in my life. I have a trust that I am exactly where I am meant to be, and I intend to live wholeheartedly for every breath that remains. ALS...