Anonymous wrote:Anonymous wrote:As a person with Tourettes Syndrome, I was very pro-disclosure. I was lucky enough to grow up in a supportive community and I found that even now giving the facts helps take the air out of anyone's snottiness, particularly if my tics are disrupting a situation. I would echo those who have suggested reaching out to the teacher/parents if possible to figure out what language they've been using with their child. I also think that thinking about strengths and weakness is helpful (though I'm not afraid of the word disability) as it helps NT kids as well as non NT kids to put themselves in context and think about how they can best learn and grow.
As the parent of a child with an "invisible" special need I would be put out by someone "reaching out" in in faux empathy. Seriously would you really ask a parent that? What kind of "language" do you use to describe your child's challenges? You seem to be lacking basic social skills.
Anonymous wrote:Anonymous wrote:Anonymous wrote:As a person with Tourettes Syndrome, I was very pro-disclosure. I was lucky enough to grow up in a supportive community and I found that even now giving the facts helps take the air out of anyone's snottiness, particularly if my tics are disrupting a situation. I would echo those who have suggested reaching out to the teacher/parents if possible to figure out what language they've been using with their child. I also think that thinking about strengths and weakness is helpful (though I'm not afraid of the word disability) as it helps NT kids as well as non NT kids to put themselves in context and think about how they can best learn and grow.
As the parent of a child with an "invisible" special need I would be put out by someone "reaching out" in in faux empathy. Seriously would you really ask a parent that? What kind of "language" do you use to describe your child's challenges? You seem to be lacking basic social skills.
OP again: I certainly wouldn’t do this re Larlo, since I wouldn’t recognize him to look at him and have never met his parents, but I definitely did it for her dyslexic friend whose mom is my friend. Just a simple “hey, Kid was saying she wanted to help Friend learn to read, I told her that’s not really her job and that Friend’s mom and dad are on top of helping Friend in the ways that work well for Friend, is there anything you’d like me to say differently or add to that?” Or if she had a friend with Tourettes I’d definitely ask the parents if there was a particular way they wanted me to explain it to her on the theory that whatever I say is likely to be parroted to the friend. But this is for kids who are her friends and whose parents I know. When she asks me about other people, I usually explain that everyone is different, including every body and every brain, and it’s not polite to speculate or to discuss strangers’ bodies.
Anonymous wrote:Anonymous wrote:As a person with Tourettes Syndrome, I was very pro-disclosure. I was lucky enough to grow up in a supportive community and I found that even now giving the facts helps take the air out of anyone's snottiness, particularly if my tics are disrupting a situation. I would echo those who have suggested reaching out to the teacher/parents if possible to figure out what language they've been using with their child. I also think that thinking about strengths and weakness is helpful (though I'm not afraid of the word disability) as it helps NT kids as well as non NT kids to put themselves in context and think about how they can best learn and grow.
As the parent of a child with an "invisible" special need I would be put out by someone "reaching out" in in faux empathy. Seriously would you really ask a parent that? What kind of "language" do you use to describe your child's challenges? You seem to be lacking basic social skills.
Anonymous wrote:As a person with Tourettes Syndrome, I was very pro-disclosure. I was lucky enough to grow up in a supportive community and I found that even now giving the facts helps take the air out of anyone's snottiness, particularly if my tics are disrupting a situation. I would echo those who have suggested reaching out to the teacher/parents if possible to figure out what language they've been using with their child. I also think that thinking about strengths and weakness is helpful (though I'm not afraid of the word disability) as it helps NT kids as well as non NT kids to put themselves in context and think about how they can best learn and grow.
Anonymous wrote:As a person with Tourettes Syndrome, I was very pro-disclosure. I was lucky enough to grow up in a supportive community and I found that even now giving the facts helps take the air out of anyone's snottiness, particularly if my tics are disrupting a situation. I would echo those who have suggested reaching out to the teacher/parents if possible to figure out what language they've been using with their child. I also think that thinking about strengths and weakness is helpful (though I'm not afraid of the word disability) as it helps NT kids as well as non NT kids to put themselves in context and think about how they can best learn and grow.
Anonymous wrote:Anonymous wrote:Why are you so hesitant to say that he has a disability? It’s not shameful. Please use the word and talk to her about all kinds of disabilities. Parents who avoid this are really annoying — like parents who pretend we are all the same race.
OP here: because from what she's told me, I'd put money on Larlo being autistic and a lot of the autistic adults I know don't like being called disabled. We talk a fair bit about disabilities without using the word -- her dad used a variety of mobility aids for a while, so we are used to that and talk about how everyone's body is different and different people use different tools to do things.
Anyway, thank you for the input, everyone. I want her to be kind and inclusive, but I don't want to speculate inappropriately about Larlo's needs and I definitely don't want to give her the idea that there's something "weird" about Larlo even if she's noticed ways in which Larlo's behavior and circumstances are different from hers. I figured you all would be the right ones to ask!
Anonymous wrote:OP- I appreciate you asking the question.
I have a dyslexic child and an autistic child and the term disability can be really loaded within both of those diagnoses/ communities. So the language about everyone’s brain works differently is generally acceptable. We also talk about how everyone needs different things to be successful- that fair isn’t equal. So one child may be allowed to chew gum or listen to music because they need that.
We talk about this so much because even children who themselves have special needs need to be taught to be sensitive to differences in others.
In your situation I agree with your approach asking her how she would feel. I would likely go further by asking her how she could be a friend to Larlo- perhaps by being an upstander and reminding her classmates it isn’t funny.
I would avoid any specific language around diagnoses or disabilities because you don’t know how Larlo’s family speaks of his needs. I think it is best to stick to the language around brain differences and need differences and how we should all be kind to each other. It sounds like you are part of a faith community, so you can also leverage the”we are all God’s children” messages from your faith tradition.
And do please invite this child to any all class parties. You can reach out to the mom to offer to let her stay and support or just make it known he is welcome.
My child was excluded from a class Valentine’s party this week because of his disability- so inclusion is a sensitive topic for many of us.
Anonymous wrote:Anonymous wrote:Anonymous wrote:Why are you so hesitant to say that he has a disability? It’s not shameful. Please use the word and talk to her about all kinds of disabilities. Parents who avoid this are really annoying — like parents who pretend we are all the same race.
Because you don't want her child going and saying in class that the other kid have a disability!
Not saying there is wrong with having a disability. But she doesn't really know what is going on.
Anonymous wrote:Anonymous wrote:Why are you so hesitant to say that he has a disability? It’s not shameful. Please use the word and talk to her about all kinds of disabilities. Parents who avoid this are really annoying — like parents who pretend we are all the same race.
Because you don't want her child going and saying in class that the other kid have a disability!
Anonymous wrote:Why are you so hesitant to say that he has a disability? It’s not shameful. Please use the word and talk to her about all kinds of disabilities. Parents who avoid this are really annoying — like parents who pretend we are all the same race.
Anonymous wrote:I want her to be kind and inclusive, but I don't want to speculate inappropriately about Larlo's needs and I definitely don't want to give her the idea that there's something "weird" about Larlo even if she's noticed ways in which Larlo's behavior and circumstances are different from hers. I figured you all would be the right ones to ask!