<?xml version="1.0" encoding="ISO-8859-1"?>
<BODY.CONTENT>
<UID>
8802260247
</UID>
<PUBLICATION>
DETROIT FREE PRESS
</PUBLICATION>
<DATE>
881226
</DATE>
<TDATE>
Monday, December 26, 1988
</TDATE>
<EDITION>
METRO FINAL
</EDITION>
<SECTION>
SPT
</SECTION>
<PAGE>
1D
</PAGE>
<ILLUSTRATION>
Photo Special to the Free Press
</ILLUSTRATION>
<CAPTION>

</CAPTION>
<BYLINE>
MITCH ALBOM
</BYLINE>
<AFFILIATION>

</AFFILIATION>
<MEMO>

</MEMO>
<COPYRIGHT>
Copyright (c) 1988, Detroit Free Press
</COPYRIGHT>
<HEADLINE>
FIGHT WITHOUT FEAR
STRICKEN FORMER MSU STAR, WIFE LIVE LIFE TO ITS FULLEST
</HEADLINE>
<SUBHEAD>

</SUBHEAD>
<CORRECTION>

</CORRECTION>
<BODY>
LOS GATOS, Calif. --  His body is limp and covered with a blanket. His
mouth moves, but there is no sound. His wife sits next to the bed, reading his
lips.

  "It began  . . . when I was playing  basketball  . . . and I kept dropping
the ball.  . . . Then in the classroom  . . . I would drop the . . . what was
that, honey? Oh.  . . . I would drop the chalk.  . . . "

  The words come slowly  through her voice, just as the disease came slowly
to Charlie Wedemeyer, robbing him of the marvelous athletic body he once
possessed. A football star (1966-68) at Michigan State, a quarterback, a
flanker,  a guy voted best prep athlete of the decade in Hawaii, a lean,
handsome man who resembled an island version of Joe Namath. Cheerleader wife.
Two great kids. At age 31? This couldn't happen to him.
  It happened.
  Amyotrophic lateral sclerosis.
  Lou Gehrig's disease.
  It is perhaps the cruelest way to die -- slowly, moment by moment. No cure.
And yet, somewhere in the months that followed,  when he could no longer lift
his arms to shave, and his students had to walk him, and soon his head needed
constant support, lest it fall into his chest -- somewhere in the middle of
this horror, Charlie  Wedemeyer decided to live.
  And to live happily.
  Which meant doing his job: coaching football at Los Gatos High School. At
first he limped. Then he rode in a golf cart, which Lucy, his wife, drove.
When speech deserted him, Lucy read his lips, passing on the plays to the
offensive co- ordinator.
  They lived. They got by.
  "One time he called a play 'Max!' for maximum," Lucy says. "And I said
'Max? Who's Max? We don't have a Max!' "
  She laughs. In the bed, Charlie makes a clicking sound.
  "Yeah . . . " he adds, through her voice. "I fired her after that.  . . . "
  How can we ever  complain about anything? How can we moan about traffic or
a lousy boss? Charlie Wedemeyer, 42, whom MSU legend Duffy Daugherty once
called "my best blocker," can hear and think as well as you and I,  yet he
cannot move a muscle, cannot speak, cannot even breathe without a ventilator.
The doctors gave him one year to live.
  That was 11 years ago.
  And in that time, his one life has touched  another -- and another, and
another. Do you remember that Christmas movie, "It's A Wonderful Life," in
which Jimmy Stewart gets to see the world had he never lived in it? What would
this town be like,  without this brave, now-withered man? Wedemeyer  did not
ask for notoriety. He kept his disease secret for several years before a
newspaper story came out.
  And yet all the kids he coached! All those  he touched! How hard it must be
for a proud man to be shaved, to be washed, to be lifted by others. Not once
did he ask for sympathy. Not once from that golf cart, unable to turn his head
to follow a  pass or a touchdown run, did he ever ask his players  to "win one
for me."
  They won anyhow. Won their division. Won their playoffs. And in 1985, on a
cool December evening, Los Gatos went to the California Central Coast
Championships, with their coach in his golf cart on the sidelines. Smaller
than their opponents, they hung in anyway, and in the final seconds, they
blocked a field goal for  a 14-12 upset victory. The stadium began to tremble.
Then to roar. A chant of  "CHAR-LIE!  . . . CHAR-LIE! . . . CHAR-LIE!  . . . "
  It would be his last game, although no one knew it. The players  mobbed his
golf cart; they dropped to their knees. He whispered the words to his wife:
"You guys  . . . played like champions.  . . . You will remember this  . . .
for the rest of your lives.  . . .  
  Not surprisingly, Hollywood has made a TV movie about the Wedemeyers (which
airs tonight on Channel 2 at 9 p.m.), a project that  has brought mixed
feelings. For while the message comes across,  a film can never capture the
subtle courage: how friends donated money for the $60,000-a-year medical
costs; how Charlie's son, Kale, would help clean the tubes in his throat; how
Lucy, an attractive  blond woman who might have selfishly felt she deserved
better, would sleep alongside Charlie's bed, her hand on his foot, so if he
wiggled it, she could wake and attend to him.
  One life touches another  and another. And eventually, fate went from
something that led them, to something that followed.
  This is truly what is meant by  "human potential."
  Eventually, the disease worsened. Charlie  lost his job. His assistant
coaches had grown weary of the burden. Eight years? The problem was -- to put
it bluntly -- he had lasted longer than anyone figured.
  So in 1986, the principal delivered  the bad news. Told him to retire, said
it was for the best. True to form, an angry Charlie mouthed his response from
the wheelchair.
  "He says," Lucy told his boss, "you're . . . a . . . bleep."
  And they pressed on. Today his son plays college football, his daughter is
in school, and Charlie and Lucy cope as best they can in their warm,
ranch-style home. There is no morbid talk. No over-sentimentality.  When he
needs to be lifted, he is lifted. When he needs to be washed, Lucy holds him
up in the shower. They talk. They laugh. 
  They live.
  "I used to be . . . so afraid of death," he says. "I  would stay awake . .
. for three or four nights . . . because I was afraid to . . . choke in my
sleep. . . . But now I know . . . I have a purpose . . . to inspire people to
. . . see their difficulties  as a challenge . . . rather than a barrier. . .
. "
  He lifts an eyebrow at his nurse. She pulls back the blanket, disconnects
the tubing, attaches an air bag to his throat, and, with the help of  Lucy and
a friend, lifts his limp flesh into a wheelchair.
  "Where are you going?" he is asked.
  He smiles. 
  "Christmas . . . shopping," he says.
  About a year ago, the Wedemeyers received  a letter. It came from a man in
Canada, who had lost his business, fought with his wife, and, in a fit of
desperation, flown to Seattle and checked into a hotel. He planned to kill
himself. In the room of his intended death, he absentmindedly flipped on the
television. And there, in low-volume color, he saw a documentary on Charlie.
Saw him lifted from his bed, limp as a rag, somehow still smiling.
  The man went back home. He is alive today.
  One life touches another -- and another and another. 
  This column is being written on Christmas Day, and I keep stalling because
I can't find a happy  ending. Barring a miracle, Charlie Wedemeyer will die,
far too soon, and where is the sense, where is the justice?
  I have no answer. Except that maybe the ending isn't always what counts in
a story.  Maybe, sometimes, it's just the courage you show along the way.
CUTLINE:
Charlie Wedemeyer and family leave the premiere showing of tonight's TV movie
on the former Los Gatos, Calif., football coach.
Michael  Nouri stars as Charlie Wedemeyer, the former MSU star who developed
Lou Gehrig's disease at age 31.
Charlie Wedemeyer and his wife, Lucy, make the best of each day of their lives
together.
</BODY>
<DISCLAIMER>

</DISCLAIMER>
<KEYWORDS>
CHARLIE  WEDEMEYER
</KEYWORDS>
</BODY.CONTENT>
