I have a group of friends who have been such great mom friends. But ever since Johns Diagnosis they seem to not be as helpful. They don’t quite understand the demands of therapy and ABA and the schedule juggling. They try to help but often I find them more annoying then helpful. They even try to talk to me about their Neurotypical kiddos problems at school and I try to help but also find myself getting annoyed at there problems as well. Does anyone else feel this way. Is it part of the process… read more
Thank you this makes me feel less alone that I feel this way. My friends are great moms but I sometimes wish their biggest struggles are only half of what I have to deal with on a day to day.
My wife wants have Nerotherapy sessions for my son who is 7 to help him with communication behavior ect. It is not covered by insurance. I think medication would be better. Has anyone used Nerotherapy before and if so how was your experience with it? Thank You
Don’t do it if you child has any signs of disassociation
My grandson is getting in trouble at school because he’s pushing or biting other kids. We’ve had many conversations, but he always gets easily frustrated and reacts this way. How do we help him?
Im so sorry to hear this. You must feel stressed about it. I agree with what’s been said. The behaviours are showing overwhelm or distress. This means staff need to be proactive. Sometimes those… read more
I’ve had some mild success with taking my lovely boy off of dairy. His BMs have improved greatly and I’ve noticed some change in his behaviour.
Has anyone found any particular book or method helpful? I saw this one and might pick it up. I’d prefer something i can keep in the kitchen with me instead of a digital version.
Thanks everyone!!
My son did like puzzles by Melissa and Doug at that age, they were a big hit.....
I am honestly considering homeschooling my children this year. Too many inconsistencies and variables with covid to feel safe to send them in to their in person school. This year its everyone at the same time the buildings, sure they will have a masking policy, but honestly kids especially adhd/asd children touch their faces a lot, and some touch all the surfaces, and masks are challenging. Seeing how it went last year when they had cohorts and masking (non delta variant mind you) we were… read more
@A MyAutismTeam Member
I am homeschooling my daughter because the public school failed my daughter.Also a little because of Covid. She gets sick fairly easily; and we have asthma & heart issues as… read more
Our son has been on it and i haven't noticed much of a difference. At school hes been even more aggressive at times. Hes taking 750mg/day and he weighs 160. Hes gained a lot since hes been on it… read more
He will sometimes make a choice between a few things if I send him a text message but often he says Idk. It seems like he wants decisions to be made for him and he will just go along with things if we tell him to. He's 18. I don't know if he just doesn't think it matters or if he really can't decide and it is a real worry for me for his future.
In home ABA therapy specifically.
I highly recommend it, the sooner the better. My son started it when he was 3 almost, 4, but I wish I would have started sooner. It made a big difference for us as a family. He is 12 now, and… read more
Now that we are in the middle of cold and flu season (and also Covid) I wanted to get some tips or advice about giving meds to young autistic children who are non-verbal. It’s a challenge for us to even know what ails my son because he doesn’t communicate well.
Right now, he’s had a bad cold for a week and I took him to the doctor and he also has an ear infection. They prescribed antibiotics in liquid form but I can’t disguise it in chocolate milk because the taste is too strong. The… read more
Some pharmacies can add flavors. Make sure to tell your doctor so they can do liquid meds. For some reason the flavor in liquid augmenting my son hates and we just have to let him sip a little and… read more