by Kacie Banegas | Jun 22, 2022 | Blog, Technology, Testimonials
“Thank you Team Gleason for helping me cover the copay for my Tobii TD Pilot with eye gaze! I was diagnosed with Bulbar ALS in April 2021. Within six months, I lost the ability to speak. I found other ways to communicate through my phone, but the weakening of my...
by Kacie Banegas | Jun 21, 2022 | Blog, Technology, Testimonials
June 21st is Global ALS/MND Awareness Day. In the U.S., every 90 minutes someone is diagnosed with ALS and every 90 minutes someone with ALS dies. Amyotrophic lateral sclerosis (ALS), commonly known as Lou Gehrig’s disease and outside the US as Motor Neuron...
by Kacie Banegas | Jun 9, 2022 | Blog, Technology, Testimonials
“I am delighted that I have finally received my customized Permobil power wheelchair! Thanks to a grant from Team Gleason, my chair also includes the ability to elevate. This feature allows me to be more independent by helping me get to a standing position to...
by Kacie Banegas | Jun 7, 2022 | Fundraising/Events, Latest News
“Dale, look what we did!” Joe Bernard turned to his good friend, Dale Clark, as they stood on stage, overlooking the Fin, Feather, Fur Food Festival. The crowd of over 1,500 gathered in Lafayette, Louisiana at the first annual F5 Festival benefitting Team Gleason. The...
by Kacie Banegas | May 17, 2022 | Blog, Technology, Testimonials
“I was ecstatic to learn about Team Gleason and the many opportunities the Foundation offers to those of us with ALS! Funding my Voice Banking and synthesizing my voice means that when I can no longer speak, my friends, family, and I will still hear my voice as I...