Today I saw two different inspiring stories that emphasized the same point: focus on what you can do, not what you cannot.
One of the first Super Bowl ads for Toyota was called Good Odds.
Within the first few seconds of the commercial, Dave called my
attention to the commercial because he knew it was going to be good. And
it was. The commercial, available at this link on YouTube,
features Lauren Woolstencroft. She beat the odds to win, not one, but
eight Paralympic gold medals. It's one minute well worth watching.
The
only thing I wish about this was that I knew about Lauren before this
commercial. We often hear so much about those athletes, the Shawn Whites
and Lindsay Vonns, who compete in the Olympics before the Paralympics.
The the coverage of the Paralympics is non-existent, which means most of
us don't know about those athletes, many of whom overcome even more
challenges than the Olympians who compete in the two weeks prior to
them.
The first story I saw today gives me hope because it
focused on an athlete who competes both in adapted sports (and from the
little bit I saw, adapted hockey seems way more interesting and
challenging than traditional hockey) and traditional sports. CBS Sunday Morning featured a high school athlete named Danny Lilya.
Danny
was born with a separated spine, which means he uses a wheelchair for
mobility. Yet he plays football. Yes, you ready that correctly. Someone
who uses a wheelchair for mobility plays football, traditional football
as I said earlier.
How?
It's quite simple.
Danny focused on what he can do. He's able to hold a football perfectly
fine. So, he holds the ball for extra points and kickoffs. He gets out
of his wheelchair, holds the ball and then leaves the field until the
next time he's needed. His parents commented that if he were to get
tackled, it would be a highlight for him and joked that they don't need
to worry about him getting paralyzed from a hit because he already is.
To
me, this story is the perfect example of focusing on your capabilities,
not your disabilities. It's not about what Danny can't do but about
what he can. It's about inclusion. How can we include others? It's about
accommodation, a very reasonable accommodation of a few extra minutes
to get Danny's chair on and off the field before and after these few
plays. What little things can we do to help others succeed, live their
dreams or simply enjoy life more?
These questions aren't just rhetorical. They're a challenge for me to always seek this mindset with Teddy and others. How can I include Teddy? What little things will help him? (And, no, a giant ladder for him to climb is not the secret to success, although he might believe that.) What can I do for others? What can you do?
Just as these stories illustrate the importance of these Lauren and Danny focusing on what they can do, my challenge to you is the same―focus on what you can do.
This is our family's journey with the rare PIGN genetic disorder Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1. When our son was diagnosed in November 2015, we were told he was the 15th documented case in the world. We've discovered more affected individuals since, but it's still an extremely rare and unknown condition since its discovery in 2011. Our hope is to create awareness of the disorder and foster a sense of community among those affected by the disorder.
Sunday, February 4, 2018
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