Shelly admitted after the campaign was over that while she wanted to
participate, she wasn’t so sure of her ability to do it. During the course of our working on our
presentation, Shelly often would criticize herself when she flubbed up, and
later she confided that she was hard on herself because in life, others had
been hard on her, and she felt like she needed to prove something. I coached her to be okay with making
mistakes, to be okay if she reworded a presentation line differently than what
was on paper. I also reassured her that if
she jumped ahead in our presentation that I had her back and would get us back
on track. With this encouragement, Shelly
relaxed more, but continued studying her presentation part until she had it
cold. The once self-critical Shelly
began patting herself more on the back as she recognized progress in her
knowing her part of the presentation.
And when I screwed up, that made her feel even better!
Together, Shelly and I decided she’d read a book about a
little girl with Down syndrome which would help students understand an
intellectual disability (which we briefly discuss in the presentation) while
nicely complimenting the very issues of fear and uncertainty we address in our talk to the children. It also highlighted the importance of focusing
on what we have in common rather than focusing on differences, a subject
important to Shelly to be addressed in the presentation. Once done with the book, Shelly would then share
her story, and immediately engage the children in asking who liked things she
liked, such as hanging out with their friends, and macaroni and cheese, and how
they have these things in common. Then, she
asked the students how they are different from her, receiving expected answers,
such as she’s in a wheelchair, and they are not, she’s older and they are
younger, etc. Shelly would then tell
them there are other differences, asking the kids who could brush their teeth,
dress and feed themselves, to all of which the students would raise their hands. At this point, Shelly would inform them that
she cannot do those things and why, thus introducing the subject of cerebral
palsy.
From here, together, we continue the conversation to explain
what cerebral palsy (CP) is, how people get it, and how it affects the body. Shelly demonstrated her limitations, while
explaining how others with CP have different limitations than her. She then explained that while she may look
different, she is unique, just like they are unique and how despite differences
between each other (i.e. better at sports than at drawing), we are all unique,
yet have things in common. We also help
students understand it’s okay to be curious, and that it's okay, not rude, to
ask people with disabilities questions.
We also briefly explain the difference between intellectual and physical
disabilities; and, how to approach individuals with disabilities. Finally, Shelly shared that people aren’t
always nice to her, discussing the R word and how it’s used to be mean, and
even jokingly to mean that someone is “stupid.”
Shelly gets "real" about her feelings with the children, helping them
understand that it hurts when she’s called the R Word, and how she feels about
people who use it, pointing out that people who call her that don’t think she
can do anything when she can, and that they are not nice people. She then helps the children understand how to
treat people with disabilities: be nice;
be respectful, and don’t be afraid to ask questions, because she’d rather
people take the time to get to know her than misjudge her because of her
cerebral palsy.
Our first “test” presentation took place in February at
Burns Elementary School before a group of older elementary students, 4th
& 5th graders (right). Shelly
admitted to being nervous because she was unsure about the school environment,
how the kids would take to her, and how they’d respond to her message. Well, let me say that nervous or not, Shelly
hit the presentation out of the ballpark!
How do I know? During
the Q&A portion of the presentation, one little girl raised her hand to ask
the question, “Shelly, will you be my friend?”
Uh, Kleenex please!
Shelly said she felt an emotional feeling of happiness deep inside because
“I touched them deeper than I realized I could touch them, and that gave me
chills.”
A Superstar is born!
In the Next Blog Entry: Fist Bumps, Hugs & Tears - "At one school, a little girl asked Shelly if anyone had called her the R word. When Shelly answered, 'yes,' the little girl’s empathy overwhelmed as she responded through welling tears . . . ."
We want to hear from you! Please share your responses and comments by clicking below on “Comment” – you may post them anonymously or using your gmail.com profile name.
“The educated do not share a common body of information, but a common state of mind.” ~Mason Cooley
Please share our blog with others via Facebook, Twitter, or email! Follow our blog! Click on “Join our Site” below.
Blog content is copyrighted property of Wendell Foster’s Campus for Development Disabilities and Carolyn Smith Ferber and/or other blog authors). Content may be used, duplicated or reprinted only with the expressed authorization of the Wendell Foster’s Campus. Permission for use, duplication or reprints may be made to wfcampus.org@gmail.com.
In the Next Blog Entry: Fist Bumps, Hugs & Tears - "At one school, a little girl asked Shelly if anyone had called her the R word. When Shelly answered, 'yes,' the little girl’s empathy overwhelmed as she responded through welling tears . . . ."
We want to hear from you! Please share your responses and comments by clicking below on “Comment” – you may post them anonymously or using your gmail.com profile name.
“The educated do not share a common body of information, but a common state of mind.” ~Mason Cooley
Please share our blog with others via Facebook, Twitter, or email! Follow our blog! Click on “Join our Site” below.
Blog content is copyrighted property of Wendell Foster’s Campus for Development Disabilities and Carolyn Smith Ferber and/or other blog authors). Content may be used, duplicated or reprinted only with the expressed authorization of the Wendell Foster’s Campus. Permission for use, duplication or reprints may be made to wfcampus.org@gmail.com.
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