It's late, hope this makes sense.
In
a way that title is true. Tell you a little story, when my daughter
was very small she had an inoperable brain mass in the middle of her
brain, inside that little pocket of liquid approximately in the
sector between the temples and the very middle/top of the scalp. It
was the size of a man's thumb and in addition my daughter had a
seizure disorder. These things not only meant she was, “dying”
they also meant that what little time she had to live was spent in
Miami Childrens' Hospital.
The
amount of time that most kids spend on the playground my daughter
spent between neurologists and telemetry labs. She spent more time in
hospital beds than she did going to school. This was my daughter's
life and though she'd never known anything different than this meager
existence, she hated it with a passion. In school, you see, were
other kids. In school there were toys. School had a library, a
playground, an art room and fun. She couldn't even get out of bed to
go to the bathroom, much less the hospital's play room. Ten leggos
and three comic books get boring after a while. And back to back
elongated hospital stays afford you very few visitors.
I
vividly remember holding her as she screamed hysterically when her
hair started falling out and I remember the pact I made with her...
if she lost all her hair then I promised I would shave my head. One
of the other teachers called that stupidity and vanity, telling me
that if she lost her hair I would be a responsible parent and buy her
a wig. (I'm not real sure why that woman thought that hiding from
your disease is helpful but needless to say she wasn't invited back
to our room.) Anyway I watched my normally happy child grow sullen.
She sunk deeper and deeper into depression. She got sicker with that
mood. It didn't look like she would leave there this time.
But
then for no reason some woman with ebony hair and dark, deeply
swimming eyes visited our room. She didn't know us. She brought Sarah
a blue, stuffed monkey. The thing was pitifully small. It was
handmade.... and not very well made I might add. She gave this toy to
my daughter, who immediately perked-up when the woman announced that
this was a “Wednesday present.” Sarah's EEG returned to normal
by the end of that day. She was home in a week, and even though she
went back in 2 weeks, it didn't matter. She no longer minded the
endless tests and labs. That gift changed her mind-set and her
mind-set changed her healing process. Random acts of kindness. She
still had that toy when she was 18... even though it was torn-up by
then.
Years
later I tell this story, the beginning of my Bibbity Bobbities, the
dolls I make for charity. Some say it is a waste of time. My dolls
have been called ugly. My dolls have been criticized endlessly...
people have even told me to take a sewing class or add mouths or...
and the list goes on. But that doesn't matter to me. My dolls I pray
will change the course of a child's life simply because I cared. My
dolls I pray will change the hatefulness of a disease, make children
forget (if only for a little while) to suffer and instead just be
kids. A little love helps us heal sometimes.
To
all of those nay-sayers and haters who criticize those silly dolls,
those random acts of kindness, I say, “Perhaps you have too much
time on your hands. I use my spare time to try to help others. And
you?”
And
so you see the Rag-doll people I create sort of evolved from a little
blue monkey. I suppose that means that the universe is not without a
sense of irony, huh?
That's
my side of it,
Angel
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