Meet Benjamin
Free To Be
Photo of Benjamin provided by his family |
“Celebrate your son every
day” were the wise words spoken to my husband and I from a dear friend during
the first shaky weeks of our son Benjamin’s life. He was in the NICU, and we
were trying to process his diagnosis of Down syndrome and multiple early health
complications. That was over seven years ago, and my friend’s words continue to
resonate within me. I have celebrated my sweet son and each new milestone that
he has worked so hard to obtain. I have celebrated his smile, hugs, and contagious
laughter. I have chosen to celebrate on the difficult days when grief over his
delays and struggles tries to creep in. Overall, I have simply sought to enjoy
my beautiful son.
As I contemplated what to
write about Benjamin for this “I Can” series, I considered the different
milestones I could highlight. I considered his daily activities and routines.
However, I found my heart being pulled in a different direction. In honor of
Down Syndrome Awareness month, I want to highlight and celebrate my son’s wonderful
ability to be fully present in the moment and to be fully himself at all times.
In his simplicity, Benjamin has no pretense. He is free to be himself and
express himself in all places and with all people. He is able to experience the
joy of the moment and to express his joy unhindered. He is able to delight in
the simple things—a song, an embrace, a delicious meal (he loves to eat!), or
spinning in circles until he gets dizzy, giggling all the way!
We are all human be-ings, but in our society we seem to be more intent on the
expectation to be human do-ings. When
we meet a new person we don’t typically ask, “Who are you?” but “What do you do?”
We find such identity in outward accomplishment instead of inward value. I
value Benjamin for who he is, regardless of what he can do. There is much I can
learn from my son and his profound simplicity. If only we were all more fully
free to simply be!
This post is for Down syndrome Awareness Month where bloggers write for all 31 days of October for Trisomy 21. During the month of October, the NDSS asks that we celebrate people with Down syndrome and make others aware of abilities and accomplishments. Individuals with Down syndrome have abilities that need to be celebrated!
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