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 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 Emily Elizabeth Cornett | Dec 24, 2019 | Adventure, Blog
December 24, 2019 By: Lisa Gamboa ALS is an unforgiving disease. It robes families of everything. However, there is usually someone that will give you some hope, and for us that someone has been Steve Gleason and his foundation. Steve is an inspiration for all. Public...