In a post below you said this:
One common Asperger trait is the inability to retell a remote event. Given issues with expressive language, theory of mind and central coherence many with AS, who seem quite intelligent otherwise, are unable to share what happened because they can't effectively process or reconstitute it for others.
My son is struggling at school during their "writer's workshop" time. During that time, they are supposed to write a story about an event that actually happened to them. He often times cannot get started because a) he can't come up with a topic; or b) he doesn't have all the details of his story perfected in his mind.
We have started keeping a little notebook of topics for him to write about during writer's workshop. We just started this week, so we haven't had a chance to see if this is working yet.
In the meantime, I would like to do so more research on the information you provided above. Do you have any good links to information on this topic? Or can you tell me more about building those skills in kids with AS?
Thanks!
Re: -auntie-
Inserting yourself into the consequence is probably ineffective right now if he hasn't had good Social Behavior training. It would be better to focus on his personal consequence- getting lost, falling in with bad people and never seeing you again than you being upset not to see him again.
B has been in different private therapy social skills groups. They have been really effective in helping him to learn social rules. He is getting there, it just doesn't always come with out help. I am working through my friend's copy of, You are a Social Detective, right now.
The classroom wouldn't have to be "noisy"; he could be equally distracted by someone walking by on the sidewalk 50 yards away. With ASD there is always an overlap of attentional issues. This could be a function of ADHD or a function of anxiety. Or it could be both. Sometimes the distraction comes from within- DS could and would live in his head at this age where he would revisit movies or IRL trips to train museums and effectively tune out real life. For DS, an SSRI helped him get unstuck around compulsive and intrusive thoughts around special interests and what if...? thinking.
This is my son too. He is a little builder, so he is constantly going back and asking questions like, "Remember when we were at_____, I wonder what kind of support structure was used to make that building so sturdy." This often times comes out during the middle of another conversation we are trying to have. It is really difficult to keep him on track during conversation, but I, perhaps falsely, assumed that this was more do to the AS.
I didn't see ADHD in my son early on. It was always there, running in the background, but I was able to expain most of it away as a AS. It's a funny thing, when you're looking at dysfuctional behavior, it can be hard to parse out the antecedent for it. DS was sinitially dx'd by both his dev pedi and his psychologist as AS with ADHD. Part of the ADHD was based on a lot of impulsive and off the wall out of seat behavior. A year later we realized he was also dyslexic and enrolled him in a theraputic LD school that also served kids with ADHD. Once they started to repair the dyslexia, the really off behavior ascribed to AS and ADHD faded. I mean, just went away without any real behavior plan.
This is where I am stuck. What is AS? What goes outside of his AS diagnosis? I guess this is why we need specialists...
The ADHD piece, which for DS was class clown impulsivity and executive function became way more obvious by 4th grade when peers reach a new level of self rugulation and sophistication. By middle school, 90% of his IEP was support and services for ADHD.
See, I am becoming more and more aware of the issues this year. He seems to be liked by some kids enough that they will play with him, but I don't know how long that is going to last. His impulsivity is ridiculous, and the biggest concern we have had in both kindie and so far in 1st grade. He touches and grabs and blurts out and runs. I know his peers are already starting to notice the differences. I worry what that will look like in a year, or two.
Medicating? Meh. DS once said his meds help him be who he is instead of some jerk. They helped him access the instruction that helped him be his best self. We didn't make the decision until he'd had a year of CBT and we had totally tricked out his classroom. YMMV, but for us meds are an important part of the tx plan.
That is good to hear. B is starting to get so frustrated when his impulses take over. He has even told us, I know I shouldn't _______, but I can't stop my body! He gets really anxious and starts pacing around when this happens. It is good he is starting to recognize it, but you can just see the torture he is going through in those moments.
In a way, the desire to be like eveyone else can be used to your benefit. It's the kid who doesn't care who is harder to manage in terms of behaviors.You may want to rethink sharing his dx. At some point it becomes impossible to advocate for a kid who doesn't know his dx. Most districts start to include kids in their IEP meetings around middle school; it's legally required by the time they start his transition IEPs the year in which he'll turn 16. It can be hard to do the big reveal if he gets to about 10-12 because kids are hardwired for conformity at that age and the news can sometimes trigger denial and depression.
James Coplan suggests it's like adoption- you should tell a kid early on so they have ownership of the information and can understand themselves better. You want to do this earlier for a lot of reasons. Holding back sends a powerful message that it isn't something with which you are comfortable- that it is a shameful thing.
And you want him to hear it from you. Two people can keep this secret if one is you and the other is dead. He could have a school professional assume he knows or a cousin overhear and drop the bomb in a moment of anger or frustration. Some of the saddest emails I get are from adults who were dx'd as young kids but whose parents never shared. Typically they have had a hard time with relationships and employment and discover the reason when clearing out papers at their late parents' home.
There is no perfect way to tell a kid he has autism. If you're going down the oft used trail "Of everyone has their own unique brand of strengths and weaknesses", you can always add the kicker that his kind has a name. A lot of people like to use this workbook to help a child better understand their own Aspergers-
https://www.amazon.com/exec/obidos/ASIN/1885477597/ref=noism/oasisonlinasp07
We have always planned to tell him at some point. We just haven't figured out the right time or way to do it. I have been trying to prime him by talking about differences when they come up. It was funny, a while back the episode of Arthur that depicts the child with Asperger's aired. We were watching it, and I asked B if he thought he knew anyone with Asperger's (he does, other than himself) and he was very adamant that he did not. I definitely want him to hear it from us and we definitely want to tell him on a positive note, so I know sooner is better than later.
I took a quick look at the workbook and that looks AWESOME! Thanks for passing that along, I think I am going to order it off of Amazon tonight.
Thanks for all your help, auntie.
I already ordered that workbook off of Amazon! Now comes the fun of talking to the Ped about her thoughts on ADHD. Bleh.