LAKEWOOD, CO – April 2, 2019. The ALS NeverSurrender Foundation and ALS Art4the Cure sadly announces the passing of Steph Courdin, co-founder of the ALS NeverSurrender Foundation on Tuesday, March 26, 2019 after a six year courageous battle with ALS, amyotrophic lateral sclerosis, also known as Lou Gehrig’s disease. At the time of his passing, he was surrounded by family and friends. Steph was born in
When Suzanne Maguire Phillips was told she only had 2-5 years to live, she was, of course, devastated. She was 36 years old with two sons under the age of 10, and what saddened her the most was the thought that it was unlikely she would live to see her sons grow to adulthood, get married, or have children of their own. Suzanne, who
As I peruse the Facebook page of Andre Miller Sr., one thing is very apparent: This man lives a full life and is surrounded by love. With a diagnosis of ALS in 2006, Andre has had to endure many physical losses. However, he finds a way to make every minute count. He recently took a trip to Disney World, despite the difficulties of
Doug Clough and his family share their story and perspective
Although all pALS face daily / weekly changes and challenges , a positive outlook ensures Doug continues to enjoy life & family #ALSNeverSurrender. Thanks for letting us share your journey .. we all hope it will be a long one.
Welcome to the foundation, this will provide some background and context on why the foundation was created.
Our Goal – To create the 1st ever ALS BioMetric and Telemetry Patient App
ABOUT THE ALS RESEARCH APP
Can we make a difference by joining together to track the symptoms of motor neuron disease (ALS)? We believe it will !
Become our partner in research today!
Beyond the Ice Bucket – Whether you have ALS, know