Laughing At My Nightmare is teaching children that all people deserve kindness and respect, regardless of their differences, while supplying free equipment to people living with muscular dystrophy!
What do we do?
No More Nightmares: In January of 2015, Laughing At My Nightmare, Inc. launched a new program designed to help people with muscular dystrophy. We call this program, No More Nightmares. The goal of No More Nightmares is to provide people who have muscular dystrophy with important equipment and technology to keep them living awesome lives!
Not So Different Program: President and co-founder of LAMN, Shane Burcaw, is the author of Not So Different, a children's picture book that answers everything kids want to know about living with a disability. Shane now visits elementary school classrooms all over the world for a once-in-a-lifetime opportunity for students to learn from an expert in disability awareness!
Your generous support helps us to continue our impactful, important, and vital programs!
Laughing At My Nightmare, Inc.