About a month ago, Riley started complaining about physical education (PE). At first it was subtle - "there's too much running." But after a few days I noticed that his head sunk a little lower on PE days. He also talked about frequently getting a drink of water, which we suspected was a covert way of resting. Eventually he came out with it: "I don't like PE and I get too tired." We encouraged him to tell his PE teacher that when he needed a break, and we reminded his classroom teacher about his condition. Both of them have been very aware of Riley's limitations.
But one day, Riley reported to his after school care instructor that the kids had been picking on him and calling him "slowpoke." We discussed it with him one evening and he broke down in tears as he talked about how hard PE was, and how much he wished he could run and jump like the other kids. We asked him if it would be okay to have a meeting about it with his school, and he agreed.
We decided it was time for a Section 504 meeting at Riley's school. Federal law gives children with disabilities the right to reasonable accommodations that will ensure equal opportunity in school activities.
Despite the necessary legal formality, the school principal, Mr. Triska, and his classroom teacher, Mrs. Mecchi were terrific. They told us what we already knew: Riley is very strong academically, is one of only two readers in the class and displays exceptional social skills and behavior. Because he becomes winded easily, he often falls behind when the class is walking in a line, especially when they climb the hill to music, the playground and PE.
After discussion, we agreed that Riley would have modified PE. Riley will have the choice to participate in PE or an optional activity. Depending on the day, it could include: going to the library, returning to the classroom with his teacher, or even helping out in the office (I'm sure Riley will be an excellent filer!) So far Riley has chosen PE a few times but opted for library time on some other occasions. He is much happier now that he's in control.
We also decided to talk to the class directly about Riley's heart. Riley will know these children his entire life and we want him to be proud of who he is. So this morning Suzanne and I joined Riley's classroom for a circle time discussion about Riley and his heart. I started off by asking the kids if anyone had had surgery or been hospitalized, knowing that one girl recently had eye surgery. I then explained how the heart works, and we talked a little bit about that.
Then Riley talked about how he has had five surgeries to fix his heart, and the kids asked all sorts of questions: did it hurt? how did the doctors do it? did you get stitches? Then Riley read one of his favorites books to the class - Mr. Rogers' Going to the Hospital. He did great, reading several pages perfectly until Mom took over and finished the book. He also showed off his scar. One of the Dads who was volunteering today talked about how he had a scar just like that from heart surgery ten years ago. Finally, we explained that Riley's heart means he gets tired more easily and sometimes needs a break from physical activities, but that otherwise he's just like everyone else, that we're all different in interesting ways.
All in all, it was a good experience. It was amazing to see our confident little guy talk proudly about who he is and what makes him different. Although it's something we knew we'd have to face, we just didn't expect it so soon, and the recognition that our boy is growing up is another reminder that thinking about Riley's future can be bittersweet.
Wednesday, November 05, 2008
Talking to Riley's classmates about being different
Posted by Ken Norton at 11/05/2008 03:48:00 PM
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5 comments:
[this is good] I love the thought of all of those kids in a circle being curious and supportive. Thanks for sharing this!
I am thrilled, as an early childhood professional and Riley's Grammy, that it was dealt with so beautifully. You two did a wonderful thing for Riley by being upfront. Interestingly enough, children respond just like adults, when we are informed and educated we become more sensitive to how it is to walk in anothers' moccasins. I am so proud of all of you and miss you. Grammy Peg
Awww...reading this put a lump in my throat. What a wonderful way to teach his classmates about his condition and needs. I feel so proud of all of you, and I don't even know you :) Riley is so strong.
Hi guys,
I completely empathize with you - Cassidy has been going through some of the same struggles with PE and the monkey bars (i.e. not being able to keep up and feeling down about it). We did a little presentation for her class, too which really seemed to help her self esteem. The kids are great once they are informed. I'm glad that Riley is feeling more empowered now, but I also know how hard it is to watch as our kiddos struggle and come to grips with their reality. Cassidy has an IEP but doesn't have physical precautions in it, outside of those in place b/c of her pacemaker, but we may have to amend the agreement if she starts to feel low again.
You are both such great advocates for Riley! Anyway, just wanted you to know I'm thinking of you all and want to get together soon!
Gwynne
We've always said how lucky Riley is to have both of you as parents! You guys are fabulous and Riley is a very lucky little boy to have you! We're so glad that Riley is feeling better about all of this. It is so true what Grammy Peg says, a key to overcoming intolerance and cruelty is educating people and sharing information.
We miss you guys!
Love, Babs, Jonathan, Naomi & Vivian
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