By
the looks of their home, Tony and Christine Clark are raising two
rambunctious 7-year-old boys. Model train tracks and Monopoly pieces are
scattered on tables and cartoons flicker on the TV set.
But the Clarks' two sons are grown men who share only the same
interests and emotional fluctuations of little boys. Like the character
portrayed by Brad Pitt in the 2008 film "The Curious Case of Benjamin Buttons," Matthew, 39, and Michael, 42, are aging backwards.
Diagnosed with a terminal form of leukodystrophy, one of a group of extremely rare genetic disorders
that attack the Myelin, or white matter, in the nervous system, spinal
cord, and brain. In the Clarks' case, the condition has not only eroded
their physical capacities, but their emotional and mental states as
well.
Only six years ago, both brothers were holding down jobs and
growing their families. Today, they spend their days in the care of
their parents, both in their sixties, playing with Mr. Potato Head,
fighting over Monopoly, and in rare lucid moments, struggling to
understand why their lives have changed so dramatically.
Before the Clark Brothers were diagnosed, they were
living independent lives. Michael served in the Royal Air Force and
later became a cabinet maker. Matthew worked in a factory and was
raising a teenage daughter. Tony and Christine, meanwhile, had retired
and moved from the UK to Spain. Then in 2007, both of their sons fell
off the radar. They stopped returning their parents' calls and texts,
and as the Clark brothers' conditions developed, their lives fell
apart.
As of April, when the Clarks were first written about in the British press, their mental age was 10.
"We will be out walking and things which might interest a toddler
interest them, the other day we were walking home when Michael saw a
balloon and pointed it out to us," father Tony Clark, told The Telegraph
last spring.
Today, the brothers are even younger mentally.
"Just like small children, they wake up a lot during the night," mom Christine said in an interview published in The Independent this week. "I was up seven times with them last night."
After learning of their diagnoses, Tony and Christine returned to the
UK and moved in with their sons. Their daily struggles as a family have
been chronicled in a British documentary, "The Curious Case of the Clark
Brothers," airing Monday in the UK.
Earlier this year, Matthew became a grandfather, when his daughter had a
son. But the news for the family was bittersweet, as the Clark
brothers' mental age continued to creep backwards.
"There's no return to them being cute little boys," said Christine, who
regularly manages their tantrums and fights over Monopoly. "They're big
strong men—and that presents a quite different set of problems."
More recently, even their physical strength began deteriorating.
"A few weeks ago, they could still manage with a knife and fork, but
now that's getting too difficult for them—they get the food onto their
forks, but somehow it all falls off before it reaches their mouths," she
said.
................................................
Now walking is the next hurdle; Matthew is already confined to a wheelchair.
"The likelihood that they're on a terminal course is fairly certain, but who knows?" says Dr. Kintner, who is familiar with the Clark case but didn't meet the brothers. "If they were citizens of U.S., we'd try to get them to the National Institute of Health for diagnostic work, but in the UK the system is different. There is no comparable organization with genetic diseases, so it's a little more difficult there."
"The likelihood that they're on a terminal course is fairly certain, but who knows?" says Dr. Kintner, who is familiar with the Clark case but didn't meet the brothers. "If they were citizens of U.S., we'd try to get them to the National Institute of Health for diagnostic work, but in the UK the system is different. There is no comparable organization with genetic diseases, so it's a little more difficult there."
Dr. Kintner estimates there are several million cases of one of the
estimated 40 types of leukodystrophies in the U.S., but an exact number
is hard to pinpoint. The different forms of the disorder are still being
identified and tests for each known type are still being developed.
"It's going to take a long time," says Dr. Kintner. "I hope in my
lifetime I see a cure for some of them."
Oh dear Oh dear **deep sigh**
Whats Wrong With You?
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