Happy World Down Syndrome Day!
March 21, 2008
(Because people with Down syndrome have 3 – 21st chromosomes,
it was appropriate that the date “3-21” was chosen!)
I was excited to hear about this day, because it gives me a chance to tell you some important things about me.
My name is Rylee.
I am 4 years old. I go to pre-school to learn things like sharing, counting, ABCs, and writing my name.
I like eating spaghetti and cheese.
I do not like having my hair cut or brushing my teeth.
I am happy when I get to read books with mom, play ball with dad and dance with my older sister.
I am sad when I have to leave the toy store.
I get mad when my little brother gets into my things.
Do I sound like other kids you know?
And, there is something else that makes me, me…
I have Down syndrome.
I don’t really know what Down syndrome is yet. What I do know is that I am more like other kids than I am different.
I am a person first.
When people talk about me, I want them to say my name first.
I am not a "Downs kid."
Because Down syndrome is only one little thing about me,
I don’t want it to be before my name.
It makes it sound too important.
I know that other people with disabilities want the same thing.
Mom says it’s called “People-First Language.”
I just think it’s nice manners.
If someone you know has autism,
they are a "person with autism"– not “an autistic person.”
If someone is disabled,
they are a "person with a disability"– not "a disabled person."
It may not seem like a big deal to you, but it is to us –
and to our families.
Mom & dad say that our words are very powerful.
What and how we say things shows others what we believe.
I hope that you believe what I do… that I am Rylee.
I am a little girl.
I like going to school and playing with my brother and sister.
I just happen to have Down syndrome.
The next time you talk about someone with a disability,
please say their name first.
It will show that person that you believe just that –
that they are a person first!
Thank you, Rylee!
*****
If you would like to pass Rylee's letter along, please email me
and I can email you her letter as a pdf document.
Thanks for helping to raise awareness!
© 2008 Carin Griffith • Disability Awareness Alliance™
5 comments:
Wow, Carin, this is beautiful. I'm going to add your blog to my blogroll. I think Rylee has a lot to teach all of us :-) BTW, there will be a moms and dads sharing sessions for slightly older kids like Rylee, too. I realized after I emailed you that she isn't under 2 :-)
Can't wait to meet you Carin! And your beautiful family!!! Save travels to Sacto!!!!
I would love to link to this/post this on Bridget's Light. Would that be okay?
Lisa, Thank you so much! I would love to have you include a link to Rylee's letter on your blog! Two more of her letters will be posted on here soon as well... please feel free to share! I can't wait to check out your blog and find out more about your family!!
Jennifer, It was great meeting you in California! I wish we'd had more time to visit! There are just so many people and so little time!! I look forward to getting to know your family through your blog! Take care!
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