Breakthrough Winter 2003
Page 5
News Notes
For more details, go to www.oif.org
Miracle Michael
raises $20,000
Tournament, organizers inspire
family to make a difference
The Miracle Michael Fund golf
outing is held annually in memory of
Michael John Shultz. Miracle
Michael was born with severe OI
and bravely battled complications
from this disorder throughout his eight
months of life. Despite more than 100
fractures, Michaels smile stands as a
symbol of how powerful the human
spirit can be, despite the obstacles we
are facing.
At the Miracle Michael IV outing,
$20,000 was raised to support OI
Foundation research programs. Held
on July 22nd, 144 golfers enjoyed a
great day of fun, sun and golf at White
Eagle Country Club in Naperville,
Illinois. Evening activities included
both a live and silent auction, along
with dinner. Many special guests were
on hand including Chicago Bulls
legend Norm Van Lier, and David
Kaplan from WGN Radio. Also
attending this years event were the
Kipperman and the Harshaw families,
as well as Dr. Peter Smith, a member
of the OI Foundation Medical
Advisory Council, Tim Caruso, P.T.
and Julianne Weiner representing the
OI Foundation.
Plans are already underway for
Miracle Michael V, scheduled for
June 30th, 2003, with a goal to raise
$25,000. Thanks again, and we hope
to see you in July!
I know first-hand
what it is like grow-
ing up with OI and
spending a fair
amount of time in
plaster casts. When I
fell and broke some-
thing, we would go
off to the ER, I would
get casted, heal and
get on with things.
Knowing that I
had the genetic con-
dition, we had our children tested at
birth so we would know if they also
had OI. Our first child, Ryan, does
not have OI. However, I never re-
ally appreciated what I put my par-
ents through until the day our sec-
ond child, Katie, was diagnosed with
the disorder.
It becomes a whole different game
when your baby girl is affected.
Upon learning the news, there was
a range of emotional reactions in-
cluding denial, fear and anger fol-
lowed by the question how bad is
it?
We began the search for the an-
swer of what Katies prognosis
would be and where we should start.
Due to the rarity of the condition,
we wondered if we would even find
a local doctor that is really familiar
with OI to answer our questions.
Having been associated with the
OI Foundation through my mothers
volunteer work with the organization,
I contacted Executive Director
Heller An Shapiro.
We promptly received the name
of a specialist (Dr. Peter Smith) at
Shriners Hospital in Chicago and a
lot of great information for us to read.
So we scheduled a visit to have
Katie assessed. During the time from
when we learned the news and when
we could get in to see Dr. Smith, I
had a lot of nervous energy.
In the meantime, the Miracle
Michael golf outing was coming up
in about three weeks. The previous
year I had the good fortune of being
invited to this event that raises funds
for OI research, and had met Beth
and John Shultz, who put on the event
each year in the memory of their son,
Michael.
They showed me that you can
make a difference and a light bulb
went off in my head.
Instead of just sitting back and
worrying about Katies condition and
feeling helpless, my wife, Bonnie and
I decided to contact our friends, fam-
ily and colleagues at work to raise
awareness and ask for donations to
support the research efforts of the OI
by Steve Kipperman
OI Foundation Member
For information about how
you can help or participate
in the next Miracle Michael
Golf Tournament, visit
www.miraclemichael.org
by John Shultz
OI Foundation Member
Steve Kipperman (l) presents John Shultz with a thank-
you for the inspiration and support he found in the
Miracle Michael Golf Tournaments.
Continued on page 16