Then you would know that severity plays a significant role in when a diagnosis becomes clear. Kids with severe ASD can be identified in their second year of life and that is really helpful for them. Kids with mild and borderline levels of ASD are often not identified until there are greater social demands in school and other settings. Sixrud is not a practice that throws out the possibility of ASD lightly, so there is likely something going on with this child’s social interactions. |
What are the “outside the norm” behaviors tgst give you the confidence in her autism diagnosis? |
| My child was diagnosed early with asd (high functioning) at 3. He has inflexibility, rigid, stimming, cries easily, not perfect eye contact and miss some social cues. It took them over 1 year before they can tell me he has asd. At IEP meeting, they mention a few times that my child has asd diagnosis early because I gave them the private ados report result have IEP code updated. What do they really mean? Good that we have asd diagnosis through private evaluation early or Bad that normally kids should not be diagnosed early with asd that young especially with high functioning one ? |
You just don’t know what you’re talking about. My dd was seen by her primary pediatrician and two different developmental pediatricians, none of whom felt she had ASD. We were assured repeatedly that she didn’t, and that all of her issues could be explained by her diagnoses of ADHD and anxiety. We had a full neuropsych exam done on her at age 10 for academic reasons (she was entering a gifted program and we wanted to make sure she had appropriate supports) and that’s when she was diagnosed. One developmental pediatrician openly disagreed with the neuropsychologist, and the other said the diagnosis didn’t really matter because dd was so high functioning that we would never have known without a full neuropsych exam. We followed up by having the ADOS administered by a highly recommended speech pathologist, who concluded that dd “probably” does have autism, but she went out of her way to stress to me that she didn’t have any concerns for dd. Both developmental pediatricians and the speech pathologist all agree that autism interventions would not be appropriate for dd. The speech pathologist suggested that dd only seek intervention if she wanted to communicate more easily with peers, and even then, she felt dd just needed 1-2 sessions of one-on-one coaching. DD just came up with her own solution: she’s became best friends with a boy because she felt that boys are easier to navigate friendships with — which is interesting because the neuropsychologist said that the brains of girls with autism are most like those of boys who don’t have autism, not boys with autism or other girls without autism. |
P.S. Per the neurologist exam, her previous diagnoses were confirmed, so we didn’t replace them with ASD. |
I also forgot to mention that dd, now 14, presents like a classic case of what used to be called Aspergers, according to her psychologist. It’s just become more apparent with age. |
Poster above again. I thought about this some more, and I really wouldn't say our daughter even has an intense interest -- it's more that it's a rigid interest. So what it can look like is bossiness or stubbornness -- only wants to play babies, refuses to play games you suggest. It looks very like social play, but in some subtle ways, it lacks the back-and-forth aspect of socialization. |
Some of my daughter's anxiety went away with the ASD diagnosis itself, to be honest, after she had a few weeks to sit in the diagnosis and feel her way around a little. The incidents of her "losing it" at school and needing to isolate or get away from the classroom went down. I think it was a little bit of a relief to know that the pressure she was feeling wasn't HER, it was the way she is built, and having that, she accepted it and herself a little more, and had more trust in herself. She is still on an antidepressant and we still use anxiety strategies, and I'm sure there will be more anxiety as she gets older, but for now the diagnosis itself was something of a relief. |
Agree with this. I raised a lot of early concerns about my DS having autism. I literally was writing on this board back when my kid was very little, asking questions and trying to figure out next steps. But he hit all of his milestones on time, and maybe we got tired of being told we were being overreactive first-time parents, and we were somewhat relieved when he was doing fairly well in preschool and then elementary. Teachers in his large public school didn't really share much with us overall. His grades were fine. He made a friend or two in school. Teachers had little to say about him during conferences - he wasn't getting in trouble but wasn't raising his hand much or overly excited about learning. He was kind of just "there." Fast forward to post-pandemic, and he started having meltdowns we had not seen before. I think all the changes and increased social challenges after isolation made it so he couldn't mask anymore. Still, no one suggested ASD, and we didn't really have it on our radar. Thought maybe depression or ADHD. Online therapist was a total flop except that she finally said, "I think you should get him evaluated. His inflexibility suggests to me maybe he in on the spectrum." Instantly, we knew it was true. Got the eval at age 10 and a diagnosis. I think he falls into this same category as someone who has ASD but is pretty good at masking and is pretty high functioning. Our pediatrician and another therapist we started seeing both doubted the diagnosis when we first got it, but both now think it is accurate. I think with a girl, it could be even more challenging. |
| This thread is an example of exactly what op and others are confused about - no one - even many medical professionals - have a real sense of what hfa is. Super frustrating diagnosis in many ways |