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“ My Wonderful Dessert “
to please everyone, and it
can link us to happy
childhood memories.
“Being Able-Disabled “
mother, Cindy. On other days she
plays wheelchair basketball and
tennis, even though she is not
wheelchair-bound herself. Her
evenings are spent at PWD
Program and doing schoolwork,
such as the recent project on a
genetic medical condition for
which she selected spina bifida or
split spine as her topic.
Margaret met her first serious
boyfriend, Juan, when they
played against each other during
a wheelchair basketball
tournament. “We were complete
enemies on the court,” she says.
They met again at a Disability
Towards Inclusivity event of DTI.
Later she realized the special
connection they shared, both
having a disability.
Margaret feels that, far from
having limited her, her disability
has allowed her to do things she
Margaret L. is like any other Throughout all of these ordeals, she might not have been able to do
teenage girl today: she talks on has retained her outgoing otherwise. She says that she
the phone, deals with the stress personality and positive view of life. would not have been involved in
of schoolwork, and has a The 14-year-old attends high school sports at all if it was not for
boyfriend. Unlike many of her and is not in any special classes. She wheelchair sports, and she would
not have some of her current
peers, however, Margaret takes is allowed extra time to get to class
friendships or her boyfriend.
medication as part of her when she needs it. She says, “I get it Rock climbing, cycling, and
morning routine; and the time [teased] a lot, but I do have a small downhill racing (a kind of cycling)
she spends in the school group of friends who are great about are some of the other activities
bathroom is not devoted to fixing everything.” she is able to participate in.
her hair. Margaret has had the support of her Margaret also volunteers in an
Margaret has spina bifida, or parents as well: “I think that, inclusion program at a Davao
known as split spine, a condition growing up with a disability, the best center, helping other kids with
in which one or more of her thing that I have had is supportive disabilities.
vertebrae did not form properly, parents; without them I don’t know The prognosis, or outlook, for
leaving her spinal cord—the most where I would be. They both have most people with spina bifida is
vital component of the central always said that I could do excellent, and Margaret is
thinking about the future. “I want
nervous system—unprotected. something if I really wanted to.”
to be a doctor of some kind,” she
She has had eight operations and After school on most days, Margaret says, “though I’m not sure what
wears braces on her legs to keep works at Persons With Disability kind yet.”
them in the proper positions. (PWD) Program, an organization that
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