I am struggling to pull myself together.
It’s March 16th 2013 and I am at the Muscular
Dystrophy Association’s Muscle Walk standing in the middle of one of the Cox
Convention Center’s rooms when grief crashes over me like a tidal wave. I want
to drop to my knees, hold my head in my hands and weep.
Instead, I stand firm, hold my blaster a little tighter, and
look at the camera while a mother takes a picture of me with her child. Nobody
can see my eyes well up. No one can see me bite my bottom lip. I take a deep
breath, reach up and adjust my helmet just as another child walks up to me.
I am a Stormtrooper in the 501st Legion.
My father, Willis Al Church Jr. was diagnosed with Muscular
Dystrophy around 1995. He was in his late fifties, rather old to be one of Jerry’s
Kids. MD slowly robbed my father of his mobility, and ultimately contributed to
his passing away of squamous cell carcinoma on March 19, 2012.
He led a life of service; service to his family, service to
his country, and service to others.
He was an Eagle Scout and later a Scoutmaster. He led Boy
Scout troops all over the world being a mentor to hundreds of young men.
He was a Sargent in the US Air Force and served his country
for over twenty years, sacrificing time away from family for up to 18 months at
a time.
After the Air Force he went to school full time to become a
teacher and did volunteer work for the Disabled American Veterans before he opted
to work in civil service until he retired.
He retired early due to his medical issues. On his
retirement he thought about helping the elderly with Meals on Wheels, but
realized he couldn’t because of his limitations. He spent countless hours in
his workshop, making all kinds of toys and projects and gave them away to
anyone who asked.
At his funeral as we reflected on his life, I thought about
how much he wanted to help others, but wasn’t able to because of his health.
Even with his limitations, he still managed to enrich the lives of others. I realized
I am perfectly healthy, and I don’t do anything beyond work and family. It was
time for a change.
I think I was watching How
I Met Your Mother and saw Barney Stinson’s apartment. I saw his mannequin
sporting the gleaming white Stormtooper armor and thought “I wonder how much that
cost?” I did a quick internet search and learned that it wasn’t completely out
of my price range. Being the frugal shopper that I am, I checked countless
websites until I ran across the 501st Legion.
Turns out the
501st Legion aka “Vader’s Fist” is
a worldwide costuming organization that formed in 1997. Their authentic
costumed members are dedicated to helping the less fortunate by sharing their
love of Star Wars through charity events.
“Helping the less fortunate.” That was the key phrase that
catapulted my desire to become a Stormtrooper. Bad guys going good.
It took me over five months to order, assemble, and complete
my armor. It took another month to be approved for membership in the 501st
Legion.
I am
TK-20736. In honor of my father, I chose his birthdate
as my identification number.
In addition to the 501
st, I became a member of
JediOKC, a local group of Star Wars fans that do all sorts of charitable activities
and welcome all costumers. Through both organizations I have been part of
events that help numerous causes and fundraisers: Coats for Kids, Limbs for
Life, JDRF, Chrohn’s and Colitis Foundation, Relay for Life, and MDA. We’ve helped
entertain children that were victims of abuse or other trauma. I did the Polar
Plunge with fellow OKCJedi member Aaron Hunt to help raise over $800 for
Special Olympics. This Saturday on Star Wars Day, May the Fourth, I’ll join
everyone in downtown Oklahoma City bright and early for the Autism Piecewalk.
The biggest reward has been the impact on my life. I feel like
I am finally contributing to enriching someone else’s life, even if it’s for a
minute.
The best part about being a Stormtrooper is the anonymity,
people don’t see me, they see a widely recognized fantasy character brought to
life. And when I am under the helmet I smile wide every time someone snaps a
photo.
Well, there are exceptions. Especially on that March 16th,
when a little boy, struggling to walk because of his fight with MD, hugs me and
asks if he can have his picture taken with me. As the grief hits me, I think of
my father and hope that I am following his example.
I manage to pull myself together and smile.