Building Accessible Homes for ALS Patients: Matt's Place Foundation
BACKGROUND Matt and his wife, Theresa, started Matt’s Place Foundation just after diagnosis and have since helped raise awareness of ALS and create support for PALS (people with ALS) and CALS (caretakers for ALS). Definition: a disease in which neuron cells in the brain and spinal cord slowly deteriorate. Over time, ALS destroys the ability to; walk, speak, eat, swallow, and breathe. In this episode, Theresa talks about the needs and strategies to make homes more accessible for progressive diseases or aging in place. ABOUT MATT WILD In 2015, Matthew Wild, a 41-year-old former U.S. Marine, began experiencing strange feelings in his hands and arms, showing signs of muscle deterioration. Nearly a year of diet change and healthy eating had not alleviated his symptoms. In February 2015, a neurologist confirmed the initial diagnosis that Matt has Amyotrophic Lateral Sclerosis (ALS), commonly known as Lou Gehrig’s Disease. As a former Marine who revels in the challenge of a seemingly impossible task, Matt wanted to be an inspiration for others battling ALS. Soon after his diagnosis, Matt came up with a slogan: “Uncrushable Spirit.” WHERE TO LEARN MORE To learn more about what was discussed in this episode of the Building HEROes Podcast, please use these additional resources. • Matt’s Story at https://www.mattsplacefoundation.org/matts-story • Hope & Housing Youtube Series https://www.youtube.com/@MattsPlaceFoundation • Donate here! https://donorbox.org/matt-s-place-foundation-1