Making a difference. June 19, 2013Posted by ourfriendben in wit and wisdom.
Tags: autism, Kambel Smith, Kantai Smith, Laughing at My Nightmare, Lonnie Smith, muscular dystrophy, Shane Burcaw, spinal muscular atrophy, Survivor Evolution, The Inspire Weekly
Our friend Ben has written in the past about two boys with autism, Kambel and Kantai Smith, and their heroic father, Lonnie Smith, who discovered his sons’ talents and enabled them to create a superhero, Survivor, online. Survivor battles the League of Diseases and his archenemy, Cheeo, whose chief weapon is depression, in a series of animated features, “Survivor Evolution.”
Their website is called The Inspire Weekly (http://theinspireweekly.com/). If you suffer from autism or Asperger’s (high-functioning autism), if your kids do, if you know anyone who does, I urge you to discover this wonderful site, and wonderful story, for yourselves. (Our earlier posts on the topic are “Autism rocks” and “Autism STILL rocks,” which you can check out by typing their titles or simply typing “autism” in our search bar at upper right.)
Today, I’d like to highlight another blog that’s making a difference. It’s called “Laughing at My Nightmare,” and is written by Shane Burcaw, a 21-year-old who suffers from a rare and particularly disabling form of muscular dystrophy, spinal muscular atrophy, which has confined him to a wheelchair since age 2. Shane’s blog has burgeoned into a non-profit organization, Laughing at My Nightmare, Inc., whose mission is “to promote positivity and fund muscular dystrophy research” through events like walks and runs. Read more at http://www.laughingatmynightmare.com.
Frankly, people like the Smiths and Shane Burcaw put the rest of us to shame. While we’re whining about eating a bad dinner or having to wait ten minutes in a grocery line or an annoying coworker, they’re using their creativity to overcome unspeakable odds and changing our world for the better. Maybe it’s time we listened up.