My son was just diagnosed last wk w/autism. I've had concerns for awhile, especially since he's nonverbal. I'm feeling a lil confused y everyone asks me "how r u dealing w/it?" They make it seem like its the end of the world. But I'm more confused about where we go from here. Can anyone give some tips or suggestions?
Re: newly diagnosed, now what
I'm so sorry. We just received our official diagnosis in December that our daughter is moderate to severely autistic too. I'm not exactly sure where you are in the process to help you. In NC we have a program funded by the state that helps families get services for children with special needs until their 3rd birthday. Through them we've had several evaluations and examinations and they've helped us get all kinds of therapy for her. They helped me get referrals to a geneticist and a neurologist. They also helped me get her enrolled in a local school that specializes in special needs children.
I'm thinking your next step, if you aren't already doing this is to find out what kinds of therapy he's going to need. Early intervention is soooo important. Let me know if there's anything else I can help you with.
I'm curious; is there something else you wish they would say instead? I think people can have a wide range of reactions to a diagnosis and "how are you dealing with it?" sounds like they might be just trying to gauge where you are so they can respond appropriately. It's hard though when you're surrounded by people who just don't get it.
I don't know all the options re where to go next since we dealt with a cluster of mild Dx and not ASD (though that was something they wanted to rule out); for us, we got treatment recommendations first through Early Intervention and then through the developmental pediatrician when we finally got in with her. His EI has also been really valuable as a service coordinator and helping us figure out what all our options are.
I guess I just feel like were in limbo right now. We have a hearing test scheduled for Apr n need to coordinate services between both EIP n children's special.
Has anyone done the genetic testing? If so, what age or immediately after dx?
Also, is he getting evaluated through the school system? My son was at about 2y10m so they had his IEP in place by the time he turned 3 and he started getting SN itinerant teacher, OT and PT through them. (Or does the SN preschool you mentioned include the therapies?) If he had gotten the ASD Dx he would have also been placed on the wait list for ABA.
His developemental pedi says that he is Autistic. It was our neurologist she referred us to that had said both dx's.
He had his evaluation with the school Jan 14th. The stated they had 60 days to get us a report. I have been told that due to budget cuts they may not be accepting any new students into the ppcd program. However then I fall into he unknown of what can I do for him because we took him out of a mainstream pre school based on the pedi's recommendation.
Should I be looking into other options just in case the school doesn't accept new students? I was told if they don't, to go to the school board and fight it. I am so overwhelmed and confused. We have another appt wth our neurologist on Thursday and I am hoping to get more answers about what I need to be doing for him. What therapy does he need if the school doesn't accept him, do I find a behavior therapist which is partly why we had to pull him from pre k, he has major meltdowns and hurts himself etc
Sorry I am rambling but I seem to get better advice from you ladies seeing as I have no personal friends with the knowledge or experience with this.
I will also be getting the book you have recommended. I am all for as many resources I can get to use.
Again thanks so much for all your input.