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"It was the day before
His journey to the clouds began in his childhood. "I was a nerdy kid, into math, making model airplanes," he said. "I have trophies from making model airplanes."
In his early 20s, about the time MS strikes most of its victims, his symptoms began _ numbness in his fingers, feet and patches on his skin. He felt fatigued for no reason.
"I thought it was just too much studying," he said.
He graduated from
But his symptoms worsened. He recalls the February day when an MRI detected his MS.
"It was a year after I'd just gotten married; I was still on my honeymoon," he said. "It was devastating."
His doctor told him to expect to be in a wheelchair in 10 years.
"It's an unpredictable disease. It can cause depression, physical problems," said Dr.
It's still incurable but due to advances in medicines, "we've changed what MS looks like," Thomas said.
How people respond to the drugs varies, Thomas said. But medication reduces the likelihood of bad results, he said.
Garrett sank into a two-year depression after his diagnosis.
"Cranky would be a nice way to say it," he said. "That's how depression is. You sit around, you don't want to do anything, you have an incurable brain disease and feel sorry for yourself ...
"I became a nasty person. My wife threatened to leave me if I didn't change. I had this ultimatum and I knew I had to turn it around."
For the first few years, Garrett fought the disease by exercising, eating a healthy diet and using the early therapies that eased some symptoms. Then in the early 1990s the
Garrett started the drug and his symptoms stopped getting worse.
"I wasn't depressed any more," he said. "I thought about building my airplane. I said, 'I'm going to do it.' "
With his MS under control, Garrett got a special issuance pilot's license which required a physical checkup every year rather than every two years.
"I started flying again," he said.
Around 2000, his MS drug stopped working. He switched to one of several drugs that were on the market by then.
The same year, he learned of Team Copaxone, a group sponsored by
In 2001, he bought an airplane kit from
The day before
Now, when he makes visits for Team Copaxone, he flies in. He tells people that a man with MS built the airplane and flies it.
"I'm not there to tell people to use Copaxone," he said. "They can use something else.
"I'm here to tell them, you can keep this thing at bay if you stay on medications and live a healthy lifestyle. And don't give up your dreams."
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(c) 2010, St. Louis Post-Dispatch.
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Distributed by McClatchy-Tribune Information Services.
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PHOTOS (from MCT Photo Service, 202-383-6099): dreams
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