This is the Parsons
family. I've told their amazing story here before. They
adopted Zion almost three years ago.
I remember the call.
They were vacationing as a family and I called interrupting birthday
celebrations.
"Do you have a
minute? I'm calling because there's a baby in the hospital who needs a
family..."
I went on to tell them about a little
guy, less than three pounds who was left alone in a hospital NICU. His birth
mother was not in a season to parent and didn't even know she was pregnant when
she went into labor 11 weeks early.
I remember talking with Jeremy and
Ashley very candidly about how fragile he was and all of the unknowns of his
future. They knew exactly what they were walking into when I led them several
days later up to a little isolette in the NICU to meet their son, Zion for the
first time.
And I watched as instantaneously they
fell in love with him.
That phone call three years ago
interrupted Jeremy and Ashley's lives in more ways than they could have
imagined. Since then they have almost lost Zion, celebrated Zion's ability to hear when
they thought he might be deaf, and have gone through countless therapies,
surgeries, and treatments.
And at their last doctor's appointment,
they got the diagnosis they anticipated but was still
earth-shattering: Zion has cerebral palsy. (You can read more about his
diagnosis here.)
But Zion coming into their lives in the
surprising way he did has never been an interruption to their family. This
little guy is so loved and cherished by his parents and doting and protective
big brothers. When they received the call that changed their lives forever they
had no idea what was ahead. But Ashley will tell you in a heartbeat that she
wouldn't change being Zion's mama for anything.
As the gravity of this diagnosis
continues to sink in, so has the revelation of the further care that Zion will
need and their desire to provide the best possible support for him. And it's costly. In addition to the medical bills they are
facing, the school that would provide the best care and therapy for Zion is expensive.
As Ashley wrote last week:
We
have no control here. We don’t hold the cards. We don’t get to call all the
shots. We can’t predict the future or change the past. We can’t even change the
hearts of the social workers so they want to help our son instead of just win
the money battle. We can’t make $700 appear magically each month so we can send
him to the school where his therapies would continue and he could be around
other kids like him. We look at the sign on my wall and realize it’s not
completely true. because we can’t do this. The only way we are going to keep
Zion alive, parent Zion well, and see his needs met is if God does all of this
for us and through us – moving mountains we can’t move, and giving hope we
can’t find within our own efforts.
I wanted to share a
way we can help. We can partner with God and this amazing family in moving
mountains for Zion. Ashley, Jeremy, and Zion could use prayers from all over the world. His life has already been one miracle after another. And you can check out a practical way to help here. For more of their story, you can follow their blog at We Are the Parsons.
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