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 Suzanne Alford | Jan 20, 2024 | Fundraising/Events, Latest News
Louisiana – Show off your support for Team Gleason on your car! Click here to learn how to get a license plate Frequently Asked Questions: I live out of state, can I buy one? The vehicle must be registered in the State of Louisiana, and title fees will...
by Suzanne Alford | Jan 9, 2024 | Latest News, Resources, Uncategorized
Share your voice with the Speech Accessibility Project!Now recruiting individuals with ALS to help speech recognition tools understand diverse voices, including those affected by ALS. The University of Illinois Urbana-Champaign will safeguard your personal information... by Suzanne Alford | Dec 14, 2023 | Fundraising/Events, Latest News
December 14, 2023 Dear Friend, A universal truth that unites us all: We all have a timeline. Most of us don’t live like we have a timeline. When I was diagnosed with ALS in 2011, I was given 2-5 years to live. For me, that was not okay then, and that is not okay... by Suzanne Alford | Dec 3, 2023 | Latest News
Team Gleason is dedicated to preserving independence through access to technology. In the face of diseases like ALS, which threaten the ability to speak, innovations such as Apple’s “Personal Voice” can help individuals sound like their unique, authentic selves in...