I remember reading a quote
somewhere that said, “The days are long but the years are short.” As a busy mom
of four, this quote really resonated with me. This past fall was no exception
as my husband and I sent our oldest off to college, another son started high
school and the baby of the family boarded the bus to Kindergarten. To say we were overwhelmed would be an
understatement. It truly seems like
yesterday that I was forever stuck in the sleep deprived trenches of
parenthood. Those days seemed to have
lasted forever. So how can it be that our life is now so different than the
life we used to know?? Well, That’s how life is. We don’t realize on a daily
basis, but it moves so quickly.
Recently, I went to Jenny and
Rick’s for our first Sal’s Pals meeting of the year. It promised to be like so many other meetings
where we tackle obstacles, bounce ideas off each other and brainstorm new
avenues to ensure a successful event.
However, there was a different feel this time, an uneasiness you could
say. There we were, gathered in their
living room planning our 14th dinner/auction when Jenny and Rick
asked us to go around the room and state why, we personally, felt like we
should continue on. This made me think
back to how I became involved with Sal’s Pals.
Jenny and I were and were working
together at St. Lukes Hospital and we were both anticipating the birth of our
second child. Each of us was expecting a
boy and dreaming of who they would be and what they would become. I delivered, Ryan, a healthy baby boy on March
3rd 2001 and was filled with excitement when Sal was born on August
4th. My excitement was
quickly replaced with confusion and fear when Jenny called to inform me that
Sal was diagnosed with Cystic Fibrosis.
Having a son just a few months older, really made my heart ache for
Jenny and Rick. I couldn’t comprehend how anyone could move forward after
learning their beautiful baby had an incurable disease. I quickly realized that I didn’t know my dear
friend as well as I thought.
Jenny and Rick didn’t shake their
fists at God, instead, they made the decision to be a part of finding a cure. They built our team, Sal’s Pals, out of a determined
group of family and friends and devoted their lives to educating themselves
about this horrific disease. They made
the complicated medical terms their second language that they use them like professionals
to educate the team they’ve built. We may not fully understand what all these
terms mean, but we do fully understand how they affect Sal’s world and Sal IS
their world. So they fight. We fight
together. It’s not an easy fight either. Raising money to find a cure for your
child’s disease is not taken lightly. Jenny and Rick and so many members have
made this their full time job, on top of their full time jobs not to mention
the families that they are raising.
Dinners that feed hundreds of people, wine tastings, golf outings,
casino bus trips, just to name a few, all need planned year after year. The
daunting tasks of collecting donations, organizing volunteers, setting up and
tearing down can really make for long days.
Days that probably seem to never end.
I could see it in their eyes, that night of the meeting, all these years
in, that they’re tired. Everyone’s
tired. But Jenny and Rick shifted the focus of the meeting to Sal’s future and
our mission statement and we were motivated as a team to continue on clinging to
hope, prayers and miracles.
Sal is a handsome, hilarious, smart and witty
young man. He is healthy despite the disease that lingers underneath. He too fights alongside his parents and the
team that is named after him. How can it be that it’s been 14 years??? 14 years
since we learned of Sal’s diagnosis, over a million dollars raised and millions
of laughs and memories that have been shared with our team. A team that is lead
by two warriors who have taught the world what it is to love and to fight. The
future is bright for Sal and the thousands of others with CF because of people
like Jenny and Rick, who patiently and relentlessly give of themselves to find
a cure. Though it can be exhausting, monotonous and at times uninspiring, they
press on. Because, not unlike child rearing, the daunting days quickly reveal
the beautiful years that have been dedicated to a miracle. Until there's a cure,
Angie O
4 comments:
Angie, thanks for telling your SalsPal's story. I suspect lot's of people share many of your same thoughts but just don't know how to express them as well as you have here. Nice blog.
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