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 8, 2022 | Adventure
Team Gleason was thrilled to send San Diego locals Derek, his wife Amelia, and their close friend on an accessible private tour of the San Diego Zoo. March 2022by Amelia Ray Derek has not had a chance to travel or get out much due to being very busy working and...
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 20, 2022 | Adventure
February 2022by Sem and Luda Lederman My husband Sem Lederman was diagnosed with ALS in March of 2014. He has lost so much in the last 8 years but this horrible disease cannot take away his spirit! Team Gleason’s motto “No White Flags!” is exactly how Sem approaches...
by Kacie Banegas | May 13, 2022 | Adventure
March 2022by Lilly Ortiz My favorite part of the trip was the overall opportunity that we had to go as a family and enjoy my mom, Lourdes, while she can still walk some. Her mobility is fast becoming limited. The first day we were able to get her on the beach was...