I had to share this. It was a great little laugh for our family.
We had an experience at a local restaurant right after Clay got diagnosed. This woman proceeded to tell us that a friend of her daughter had found a "cure" in Canada using cinnamon. She told us to look into it an "get Clay cured!"
And we have had people hold up treats, in front of Clay, and say "Oh I guess you can't have these."
And we have had people say, right in front of Clay, "He has the really bad kind."
So just remember if you are unsure of a child's disease, learning difference, or physical issues be upfront about NOT knowing. We have wonderful people who say "I don't know anything about type 1, or what's the difference between type 1 and type 2, or what do I need to know about Clay?" We love these people.
The other people...well see for yourself.
Oh that is great! I like when she says that her daughter can't eat cookies made from poison! haha!!!
ReplyDeleteJust think, when you add an african american child into your family you get to hear even more awesome questions!