It was the eve of Noah's father's 40th birthday. Fall heavily upon us,
leaves dropping faster than I could count them as they drifted
peacefully towards the grass. Chris and I were outside for a moment
evaluating the weather changes as rain was in the forecast. His eyes
heavy with a touch of sadness could have spoken what I already was
feeling too. The understanding that we're both getting older -
quickly. And none of this is getting any easier. In fact, it's only
getting harder. We don't often have conversations about it. But it's
always there never far from the surface of our daily thoughts.
A
growing child that requires a lot of care. More care than he ever even
needed as a baby. We can no longer make due with baby strollers and
toddler bath tubs. Now all of Noah's equipment is specialized, most
customized and costing thousands upon thousands of dollars. Sometimes
if we're lucky Medicaid will fund some of it, but more times that not,
denials hit us left and right. There are no more lines of credit,
nothing to stand between us and the deep blue sea. No financial line of
defense. And no way to really financially keep up with Noah's needs. He
has specialized diets and purees, medical supplies that Medicaid
doesn't cover; saline swabs, toothettes, special soaps and creams for
his skin... the list is endless. Then there are the big things Noah
needs, a stand to roll his adaptive chair from room to room, an
estimated cost of nearly $980, A bath chair that exists in the UK that
would cost about $4,000 for me to get here for him, then there are the
things that would allow Noah to participate in family activities; a
specialized custom Axiom Improv Seat with Abductor so that we can walk
and run with Noah, a sensory play area so that he has something to do on
the floor other than shred large coloring books that I get him from the
dollar store, his out of pocket therapy costs, some therapies being abandoned altogether because there is no money... and the list goes on and on.
The worries mount as the years go by. We can't
plan for a secure future, not for Noah - not for any of us. There is
no life insurance policies, no thriving retirement accounts, no burial
plots, no savings accounts. Nothing. We have nothing and will always
have nothing. Which is hard for me to accept as once upon a time I
built a nest that was filled with lots of security, I thought that I was prepared for
rainy days and hard times should I ever encounter them - but there is
nothing quite like the perpetual storm that hits you on the special
needs journey.
Chris positioned himself on the outdoor bench
that sits on our patio. A place that he sits often with Noah nuzzled
and cradled into his side for support. A man that wants nothing more
than to do the best he can for his family, his blue eyes with a hint of
gray in the light of a cloud covered sky looked worried. I lacked the
proper words to ease his pain and concerns, the fear for Noah's future.
I feel it all too.
We both sometimes catch ourselves dreaming
beyond where we are. But know there is no way to ever get there. It's a
bit like being continual state of being stranded. And it weighs heavy
on any parent when you fall short from meeting your child's needs. And
we're of course also trying our very best not to short change our
typical child along the way even though he has an older brother who's
monthly expenses are the equivalent to a second mortgage.
Feeling
the seasons change also reminds us that the holidays are fast
approaching, Thanksgiving and then the ultimate gift giving holiday...
Christmas. The holiday that always hits me emotionally the worst since Noah's birth. Yet, you probably wouldn't know it, as I camouflage it well. I've
become a master at smiling on the outside when I can be crumbling in
the inside and continuing to sing those holiday tunes. I can walk around like that without anyone even noticing.
It must have been on Chris' mind too as he lowered his head to look
towards the ground and said "let's skip giving each other gifts this year so we can just focus on the kids." He
also knows how important it is for me to give five surprise gifts to
other special needs children each year and that I don't want to have to
give that up.
And it's all very true, those who generally have
the least give the most. I gently nodded in response to his
suggestion in agreement. There is nothing more that either of us
really want other than to provide for our boys - and all the things that
are always out of reach for Noah. We know it's only getting harder, but we're trying as hard as we can to grow stronger.
Love,
Noah's Miracle by Stacy Warden is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.