My Son Is 4 He Was Diagnosed With Pdd-nos When He Was 1 1/2. He Still Doesn't Talk He Just Makes Sounds And I'm Worried. Will He Ever Talk? | MyAutismTeam

Connect with others who understand.

sign up Log in
Resources
About MyAutismTeam
Powered By
Real members of MyAutismTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
My Son Is 4 He Was Diagnosed With Pdd-nos When He Was 1 1/2. He Still Doesn't Talk He Just Makes Sounds And I'm Worried. Will He Ever Talk?
A MyAutismTeam Member asked a question 💭

He had early intervention from 1 1/2 to 3yrs then he aged out. They provided speech and OT for him 3x a week. Once that finish I started out patient therapy they see him 2x a week for speech and OT. He's suppose to start school in September and I'm absolutely terrified to send him. I have a small cousin who's 5yrs old w/ aspergers and one of his teachers aides smacked him in the face. She got fired for it but that happening has made me more scared. But I know keeping him home is hindering the… read more

posted May 27, 2013
•
Be the first to like/hug
A MyAutismTeam Member

Is your son enrolled in your state's Long Term Care program? Does he get medical insurance through medicaid? You should talk to your caseworker about doing an ABA program. About school, does your son require a one-on-one aide in the classroom? Both of my kids have one-on-one aides, the youngest in her special needs preschool room and the oldest in her mainstream kindergarden room. If you child is not independent in the bath room, is an elopement risk (will sneak away/run away) and can possibly be violent towards other children then the school district should not be able to refuse to give him a one-on-one aide. We walked out of our first IEP meeting without signing and returned with a hired advocate from Phoenix to show them that we were serious and would not send our girls to school without one-on-one aides. Because we have a robust home-based ABA program with college and graduate students providing the one-on-one hours at home we insisted that the IEP state that our kids need ABA trained one-on-one aides which meant that they had to hire the girls from our team whom we have hand picked and have paid to have trained by our BCBA. It can take some work and planning and a bit of an expense if you hire an outside advocate like we did, but if you are scared to send your son alone I would insist that he needs his own dedicated one-on-one aide. Having aides in the classroom may not be enough. Also you can either try to have someone you know and trust hired to be his aide, or you can develop a personal relationship with his aide so that you can discuss what happened daily. We have a notebook that goes back and forth from home to school where I write in if one of the kids didn't sleep or has had some change in routine or something and the aides write back about what happened at school that day. It's very reassuring since my kids can't yet tell me themselves about everything that happened.

posted May 30, 2013
A MyAutismTeam Member

Hi there!

Your son is so cute in that picture! I just love the joy on his face!

It is scary sending your son to school for the first time. Is it a preschool?

Listen to your heart. Do you feel like it's right and he may grow from this? If he starts school and it falls apart, can you pull him out? Can you wait another year? Do you want to?

Listen to your heart. Trust yourself.

Communication will come. It will. There is a great book called more than words by Fern Sussman. I used it like crazy in my therapy sessions.

It's a bit pricey but maybe you can find it used. It sounds like it would be a great one for you.

For now. Get down on the floor. Play with him like I know you already do. And try to let communication happen in his world. Play with whatever he is focused on. Join him. Be patient. Wait and watch him. Try to really understand what he is already telling you with his body.

It will happen. you are doing great.

In love and support,
Laura

posted May 28, 2013
A MyAutismTeam Member

You cannot force the child to speak until they are ready and sometimes that takes a long time. My daughter is 7 and still non verbal. She uses PECs and also sign language which seems to help out with the aggression because she cannot tell us what she wants or needs. This on top of speech therapy seems to work the best. If your child is truly non verbal no medication or supplement is going to work unfortunately we have been there and done that and all it we got was a waste of money.

I can understand you’re being worried about school because your child will not be able to tell you if something happens, but you will know by your child’s actions that something is up. The truth is that most schools and teachers are good and would not consider hurting your child, but we all hear of the bad ones. I would worry more about your child getting the services they need in school rather than them being hurt there.

posted May 28, 2013
A MyAutismTeam Member

We tried diet and supplements without any luck. She is still non verbal. It's worth a try though just keep in mind it's not for everyone. We still keep up with the supplements. She is making progress everyday. We started with pecs and then moved on to an iPad with the proloquo2go app. Now she is in the process of getting a more sufisticated speech generating device. If I can get medical to fund it cause it's over $7000. I too was not willing to let her go to school. Looking back I'm glad I did. It wasn't till kindergarten that she was miss treated. Even though she didn't verbally tell me her behavior did. She had always been an easy going child. Well that year she started head banging and eating and smearing her poop. She only did it at home so it did take a while to put the pieces together. My advise is to pay close attention. Visit the school as often as you can and start a way of communication.

posted May 27, 2013
A MyAutismTeam Member

Have you tried any nutritional support yet? I have found that my DD's gains from speech and preschool have been of the "slow and steady" kind, while the big jumps have come as a result of adding certain supplements. Specifically, Behavior Balance DMG, acetyl-l-carnitine, and Coenzyme Q10. All of these are available over-the-counter relatively inexpensively. After starting the methyl B12 injections we saw a mild acceleration of the rate of improvement, but those are pricier and require a doctor's prescription. Some people see speech gains with Omega 3's, but we personally didn't. N-acetyl-cysteine is one of the next things we're going to try, but DD had to be treated with Nystatin for yeast first since NAC can exacerbate yeast.

posted May 27, 2013

Related content

View All
Those Of You With Non-verbal Children, Do They Make Sounds, Imitate Sounds, Jabber, Hum? Can They Say Words, But They Choose Not To?
A MyAutismTeam Member asked a question 💭
Will My 12 Year Old Son Ever Talk
A MyAutismTeam Member asked a question 💭
Child Diagnosed PDD/NOS &nonverbal, Turns 9 In July & Verbal Should He Be Retested? To See Where On The Spectrum He's Now? Is That Unusual?
A MyAutismTeam Member asked a question 💭
Continue with Facebook
Continue with Google
Lock Icon Your privacy is our priority. By continuing, you accept our Terms of use, and our Health Data and Privacy policies.
Already a Member? Log in