Wednesday, April 18, 2012

An Evening on the Island of the Colorblind


Last night I re-watched The Island of the Colorblind. It follows a neurologist and scientist on a trip to Pingelap, a small island in the South Pacific where almost 10% of the population is born with the eye disease Achromatopsia and 1/3 carry the gene for it. Achromatopsia causes total colorblindness, extreme light sensitivity, and visual acuity around 20/200.

Why would I care about visually impaired men, women, and children living on an island thousands of miles away? I felt drawn to the film because I was born with this disease. Outside the isolated community of Pingelap, Achromatopsia only occurs in about 1-in-33,000 people. It’s recessive so it tends to pop out of nowhere in families, and once it does, parents usually have more than one child with low vision. My sister Sherry has this eye problem while my sister Kristy doesn’t.

After growing up with a disorder so rare that I often find myself explaining it to doctors, the idea of a place where I would have neighbors, friends, and even teachers just like me and wouldn’t stand out as odd fascinates me. What struck me even deeper was their attitude toward the disorder. These visually impaired people get by without the sunglasses, magnifiers, and resources that I rely on, but they also grow up without being labeled disabled. The scientists had to be careful to offer things like sunglasses and magnifiers as cool tools that could make their lives easier without implying that anyone had a problem that needed fixing.

Those who had never seen color didn’t seem to miss it or feel deprived. Instead, they emphasized the patterns, tones, shadows, and textures that they did see. They obviously struggled but it didn’t consume them or hold them back. Many of the night fishermen had Achromatopsia because they see so much better after sunset. The visually impaired seemed perfectly happy and those with 20/20 vision accepted them as normal.

Their outlook got me thinking—wouldn’t it be nice if we could embrace life and others this way? Wouldn’t we all feel a lot freer focusing on what we have instead of what we don’t and noticing strengths before weaknesses? What if we decided to see ourselves and everyone we meet as perfectly normal and treat them accordingly? After all, each of us could turn the television on one day and discover that a place exists where what we thought was weird isn’t considered weird at all.

2 comments:

Barbara Hartzler said...

What a great post! This really speaks to me on a personal level since I have a rare problem with my hands that doctos don't know what to do with. Listening to Air 1 today, I heard about a 12 year old girl who won a penmanship award--and she was born with no hands!

News like that and posts like this encourage me. And I needed it today. So thanks for letting God use you. Such a blessing! :)

Jeanette Hanscome said...

Thanks so much, Barbara! Your comment encouraged ME. I'm beginning to wonder if God sees "disabilities" as the world sees them. Instead, maybe they are His creative tools for bringing out our determination, or gifts that we might not have discovered otherwise.

I pray that you will continue to see God's purpose and enjoy the person He created you to be.


Girls, God, and the Good Life

 
Designed by Munchkin Land Designs. Copyright 2011. All Rights Reserved.