If you went
to my school,
you would probably see me zipping around the halls and you would
probably
wonder who I was. Well, wonder no more. I'm here to tell
you!
My name is Margaret Jo Purk. You can call me Margaret or Marg, M.
J., or Margaret Jo, or even Miss Maggie. I have brown hair, hazel
eyes, and pierced ears. I was born on January 8, 1988, my parents
very first child.
When I was
nine months
old, my parents found out that I had Spinal Muscular Atrophy.
That
meant that I would never roll over, crawl, walk, stand, or even sit by
myself. It also meant that I would get sick often, choke
frequently,
and have trouble eating. The doctors told my parents to take me
home
and love me since I would die before I was two. Were they ever wrong!
On January
3, 1989,
my sister Emma Clare was born. We soon found out that she had
Spinal
Muscular Atrophy too. Emma and I frequently got sick, but we
still
attended preschool. When I was three, my mom was killed in a car
accident
while on a lunch break from work. That was on June 4, 1991. My
dad
took off work from A & S to take care of us and so did a lot of my
aunts and uncles. In September of 1991 Brenda came to live with
us
to take care of Emma and me. That was wonderful. Right before Christmas
of that year, I got a big surprise...my first power wheelchair! Finally
I was able to go wherever I wanted. Yippee!
My
sister Emma
The sadness
in my life
didn't end that year, unfortunately. In March 1992, my sister
Emma
died during a nap. She had a hard time living because she was always in
the hospital, and that made her sad. I believe that now she is 'free'
to
run, play, roll down the steps, and walk. Free like she never was
during
her life.
To help
heal the pain
of losing half of my family, we started to travel and visit my aunts
and
uncles. We went to Ohio, Colorado, Wyoming, and Florida in the next
nine
months. For some odd reason, after Emma's death, I became
stronger
and healthier for awhile. I continued to go to school and take
long
vacations, even making it to Iowa twice.
Elementary
School
I attended
Elementary
School for five years. During the second year, my breathing
became
weaker and I missed a lot of school. In third grade, my
doctor
wanted to put a hole in my throat to help me breathe...that's called a
tracheotomy. He wanted me to use a special machine to push oxygen in my
lungs (a ventilator), too. My father said no and so I didn't. What I
did
do was miss most of third grade because of pneumonia...it just wouldn't
go away. With the help of a new doctor, though, I was
healthy
and ready to tackle fourth grade.
Operations
Fourth
grade, and this
time I missed a lot of school, not from pneumonia, but from having an
operation
to have my spine fused. The doctors told me that I needed to have
the spinal fusion, but they warned us that I might die from the
surgery.
As you can tell, I didn't. I spent only five days in the hospital
after a twelve hour surgery which amazed all my doctors, so much so
that
one is writing a paper about me. During the surgery, the doctor
placed
a metal rod that goes from my right hip up my spine to my neck and then
back down my spine to my left hip. As a result of the surgery, I
grew to my current height of 5' 4". After surgery I lost a lot of
muscle strength in my arms from nerve damage and had to learn how to
write
and feed myself all over again. I also began having more problems
with choking and I missed even more school.
Despite
missing so
much school, I managed to graduate, to have a part in our class play,
and
to sing a solo in "Romeo and Juliet". I am now in fifth grade and
am awaiting my third power wheelchair. Now being in a wheelchair does
*not* mean I don't have likes and dislikes
like anyone else. Like other kids, I watch TV, play baseball,
listen
to music, read good books, and hang out with my friends. One of
my
favorite TV shows is Seventh Heaven because I can watch it with my
father.
The show focuses on issues that kids face today. I also like shows that
make me laugh, including: Boy Meets World, Sabrina, The Rosie O'Donnell
Show, and Smart Guy. When not watching TV or doing homework, you can
find
me listening to country music. I love it because it's not loud and
obnoxious,
and because it talks about real life problems.
Like many
kids, I collect
Beanie Babies...all types! I have over 300 beanies, and that's only
since
April, 1996. Most of my beanies have come from writing contests I
have won on-line. I also received over 100 beanies after my spinal
fusion!
My dad got me hooked on Sasha dolls, and so I've collect three of them,
too. I attended my first Sasha Doll Festival four summers ago. I
love to design clothes for them and then have my father make
them.
I also collect Noah's Arks, angels, and of course Barbie dolls. As you
can see, I am an active person. I am rarely home in the summer
time
because I travel. During the school year, I kept extra busy
attending
meetings of the two groups I belong too. As a Girl
Scout, I was incredibly active, earning 40 badges in Brownies and 70 as
a Junior Scout (as of 2000). Can you imagine how many I've collected by
the time I finished the Scouts? I've also belonged to WOW (Winners on
Wheels) for a
very long time, a scouting group for boys and girls who use
wheelchairs.
Middle
School
In middle school, there were many things I like and many
things I dislike about it. I'll start with the bad things to get
them out of the way. First and foremost is the issue of
accessibility.
This school, like many others, does not meet federal laws. There
are no regulation size elevators, accessible bathrooms or drinking
fountains;
the doors aren't wide enough and they're not automatic; there are
no safe parking spots and no handrails on the ramps...and that's just
the
beginning. These are all things that I would fix if I were in
charge.
I would also make adults take a disability awareness class, so that
they
would be more aware of the difficulties faced by people who are
disabled.
Now, onto
the good
parts. The teachers were
wonderful and were quite aware of my differences and how they do and
don't affect
my learning. I also had many great friends. I have one
especially
good friend who I can share secrets with, knowing that she won't tell
anyone.
I also have other friends that I can hang out and have fun with and not
worry about being in a wheelchair. Luckily, I am not teased
much.
When it does happen, one of the kids from my old school steps in and
tells
the other kids why I am in a wheelchair.
The worst part
about being
in a wheelchair is not being able to run, jump, or climb like my
friends.
I really dislike it when people pat my head and won't ask me questions
but will ask my father. I also don't like it when I'm out running
around and parents tell their children not to stare, but then they
stare
themselves. I like explaining to little kids why I am in a
wheelchair
and watching them figure out what it would be like to be in one
themselves.
One good
thing about
being disabled is that I don't have to wait in line when I'm at theme
parks.
And the best thing about being disabled is being able to change
people's
attitudes about disabilities one at a time. I figure that if I could do
that I could make the world more equal for everyone.
In the
future I would
like to complete six goals:
First
to get a computer with an on-screen keyboard and a voice dictation
program.
When I do I'll be able to write my own stories and do my homework
independently.
It will be great to keep up with other kids in class-work involving
writing.
My
next goal is an important one...not just for me, but for every disabled
kid who has faced the types of problems that I have. I hope to
get
all the schools in my town accessible for those with physically
disabilities,
including blindness and deafness. School should be accessible for *all*
kids.
Then
I'd like to get a new power chair. I need a new chair because
mine
is too small and it won't support my ventilator (I need to use one now
when I'm sick). If I have a ventilator on my chair, I won't have
to miss so much school. A new chair would also be able to
hold
my computer so it wouldn't fall off when I do exercises to relieve
pressure
on my bottom.
Now
this one has been a life-long dream. I want to get a 'Canine
Companion
for Independence'. I believe the dog would help me become more
independent
and rely less on adults. As a teenager (when this was updated in
2004),
the dog would allow me to spend more time with my friends. With such a
dog, I would be able to pick up writing utensils, go places freely (the
dog could help to open and close doors, turn lights on and off, and to
get me help from adults when I need it.
My
next goal is a long-term one. I would like to go to college and
major
in education because I'd like to teach elementary school. I
believe
that I was given the gift of being able to teach others, and I'd like
to
help kids be comfortable with and accept differences.
My
final goal is to become a well-known children's author. I
would
like to get some of the stories I've written so far published because I
know that children would enjoy them.
Meeting
these goals,
I'm convinced, will help me to live my life to its fullest.
UPDATES
I was sick
5
or 6 times four years ago when I wrote this update, and I needed to use
my ventilator most of the day. I
also only stayed at school for half a day. I did get my new
computer
and my wheelchair is on order. I am being interviewed by the
paper
and will be on the front page!!!
I also am a
published
and paid author. I wrote an article for Mary Beth's Beanie World
for Kids, March 1999 issue and got paid for it. I also write a
bi-monthly
column for the WOW connection newsletter. And*da-dum*, there's a
newspaper
article about me at the other end of this click!
June 15
Hi there,
it's me again...tonite
is my scout award ceremony, and I'm receiving over 40 badges, two signs
and a leadership pin (first time ever a junior scout won the leadership
pin...I feel so honored!). I'm excited, too, because my
troop
and I actually designed our own badge for Disability Awareness.
Pretty soon
I'll be
out of school for the year. Two more finals, and then goodbye fifth
grade (that's my grade in 2000).
Even though I was only able to attend half-time all that year, I
was
able to keep up with all the work, with, get this, an A+ average. Bet
you can imagine that I'm smiling!
July 27
Another
exciting update.
#1, I received my new chair, and am really enjoying it....zooming
around.
I can even pop a wheelie all by myself....my dad doesn't like it, but I
sure do!!! They set my speed up and no one can keep up with me
anymore....watch
out world, here I come!!
And
#2, Guess
what I got in the mail today.....a new beach chair. I can sit in
the sand and play in the water now. I went outside and played
with
the hose and got all wet and watered the ground. I had a blast.
Margaret
Purk
Age 11
Merry
Beanie Christmas
to all of you!