Free writing… this is where I write continuously without caring about spelling and grammar. Tonight I’m just having a bit of a rambling… because today I had a nasty moment with my son Curly. He’s 4 and has autism. However, I’m not sure if tonight was him and autism or him being a 4-year-old… he’s the only child I have. This post will not be edited except for typos. I just feel like saying stuff. This post contains two sentences that may offend some readers, I apologize in advance.
From the things that people who know about my son’s diagnosis continue to say, I assume they believe that Curly has autism, speech delay and likes to play on his own… most of the time. They don’t have a clue what it means to have autism, and what it means to be the parent of a child with autism. Especially a very small child who is still growing and still learning communications skills and language.
This child of mine doesn’t fully understand a lot of things and I don’t know if it’s because he has autism. For example, he doesn’t understand why a dead piece of grass which has been pulled out of the soil can’t stand on its own. He gets frustrated, he chucks a fit, he screams and shouts. Today he didn’t understand why he can’t continue playing outside when it’s pitch dark. He was probably thinking I was being the meanest mum on Earth when I asked him to bring his bike in and to go have his bath. He rolled on the floor, screaming his head off and I’m sure the people next door think he’s a spoiled brat who wants his way.
My son doesn’t understand that just because the sun sets on us while we’re still out driving it doesn’t mean we’re buying fast food. He associates driving at night-time with getting french fries. He loves french fries. He chucks a fit and won’t get out of the car when we get home.
All this does my head in most of the time. If I’m too tired I ignore him, tell him Fine, stay in the car then. If I’m ‘awake’, fine and aware, I will try to coax him into the house or away from whatever he was doing.
But when he starts crying it’s like… like he really lost a part of himself and is crying because it’s gone. Seriously. It’s like he is emotionally hurting. Forgive this example but you know when you watch someone scream, get out of control and cry after they’ve been told their loved one has died? That’s how hard my son cries when you tell him he can’t do or have something. I don’t know, is this a typical reaction of a child or is this my son being a boy with autism?
Everything stops existing. He is locked in his own world and he can’t hear anything you’re trying to tell him. I try to hold him and comfort him. He reaches out and scratches. He kicks. Screams. Kicks and screams. This would last a few minutes too long for my head. I thought we were over this, I thought he had stopped acting this way. But lately it seems to have returned.
Sometimes Curly runs to the couch and buries himself deep into the cushions and screams “Noooo, nooo, nooo” just like people do when they lose a loved one. Like when I found out my grand father died. It scares the heck out of me this similarity. It makes me believe that he is truly hurting. I don’t understand why he would feel this way about not being able to play outside in the dark.
But then again, I don’t understand much about autism. I’m still learning and my son teaches me something new every day. This anger, this rage, it gets too much sometimes. It’s too much for a child, even. But he’s more calmer for longer nowadays. Last year Curly was full of rage. There were times when he wouldn’t sit still to have a meal at restaurants. He wouldn’t sit still for a haircut and tonight he did. And the most hurtful of all… there were times when he wouldn’t let me – his mother – hold him for a cuddle. My heart bled many times too often last year.
But since we started speech and behavioral therapy sessions and kindergarten, my Curly is ‘home’ from his own world. There’s still a lot of work to do, but he’s here. He’s more present. He’s more in our world. He’s still angry at times but he’s learning to cope. And as his parents, the Scientist and I are learning to work with him.
The house is now quiet… and I miss my son when he’s asleep. And every night when I go to kiss him while he sleeps, I say a prayer – God, please make my son a little bit better tomorrow.
If you have a child or loved one who displays lots of anger and rage? How do you cope with this? What has worked for you?
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{ 18 comments… read them below or add one }
I can’t imagine how hard it is for you and I can’t imagine how hard it is for your son. It just breaks your heart to see them in pain and feel powerless to do anything about it. You have your son doing speech and behavioural therapy which is wonderful and I’m glad you’re both finding it beneficial. Have you considered seeing a behavioural psychologist yourself who specialises in autism spectrum disorders who you can talk to about the challenges, your expectations etc. It might be good support for you but also a chance to ask specific questions and learn more about autism and specific behaviours as they arise. In our area we have a dynamic parent support group for people with children on the autism spectrum, it is organised for parents by parents. It’s a wonderful group because they learn from each others experience. If there is not a group like this in your area, you might be able to find an online community that does this. I wish you all the best. Bree
Hi Bree. Thanks for this. My husband and I were talking about this yesterday. We thought we’d ask our son’s behavioural psychologist if he provides services for parents (i.e. adults). As he knows a lot about Curly he might be able to help us cope with him. But on the other hand, I was feeling maybe I’d want to go somewhere else, somewhere separate. At this stage I’m not sure which one would be best. But yes, we decided it’s time to seek some help for ourselves because it’s affecting both of us adults. I’m lucky my marriage is not affected – yet. It’s just us as individuals stressing too much too often, if you know what I mean.
If you are ok and your husband is ok and your marriage is ok – your son will be ok. Always remember that. Best wishes.
Thanks. xx
Silly Mummy recently posted..The Best of Me: Savouring Every Moment
I wish all the best to you and your family. I haven’t any advice except to keep doing what you are doing and love with your heart.
I am in absolutely awe of your strength and your love and your honesty. You are amazing!
mummyateme recently posted..Housewifely Happiness #2
Thank you!
Hey, I like your blog name! xx
Silly Mummy recently posted..The Best of Me: Getting to Know Me
Oh I understand . I really do, and I am glad you can let it out safely here.
I have seen children who are in schools, and in my family (grandson) who cannot express themselves adequately for good communication ….but I do not have to be with a little or a big person who is having behavioural issues 24/7.
As mothers in particular we “want to make it better” and when we can’t we are so hard on ourselves.
I am glad that I have found your blog today…and want to say “good for you” you are doing a great job as his mum. He knows that too, but he can’t quite tell you.
Denyse
Denyse Whelan. Education Specialist recently posted..My 3 Blogging Success Stories
Thank you very much for your support, Denyse. I’m grateful for my son’s school and their efforts in customizing their programs for him. It’s helping a lot. I’m surprised at times when they tell me the things they have gone out of their way to do, and most of it were the ideas from the teachers, not the curriculum planners.
I’m not a mum, but I work in childcare and I have autism. Sometimes I will have complete meltdowns over silly things, and I know they are silly at the time, I feel embarrassed to be expressing myself the way I am, but I cannot stop. Sometimes I pull my hair out.
The lack of understanding as to why nightime means time to come inside may come from a very deep need to explore and know (of coourse I can only speak from my own experience) as the world looks so different in the dark, it may well be perceived as an entirely different place, with different things to explore.
A lot of what you have described seems to me to be normal four-year-old stuff, too. At least from what I’ve seen of the age group.

Cassandra recently posted..Sunday Selections- New Chapter Edition
Hi Cassandra. Of course… you are right. We tend to never put ourselves in our children’s shoes often enough to understand from their point of view. It’s hard to pause and think like that because most of the time life is hectic. You are right, my son probably wanted to keep exploring and was probably only seeing tunnel vision when I was trying to make him understand that it’s dark. Thanks for the reminder! Although of course he can’t stay outside all night, lol.
I don’t consider these things ‘silly’ really, just not the usual that I have dealt with before I had my son. I need to get used to it.
Silly Mummy recently posted..We Could Be Hindering Our Children’s Development
You are a strong mum Rhonda. I hope I would be able to do half of the things you do. ((HUGS))
I know Kate from Kate Says Stuff (not sure if you know her via twitter) has just launched a mummy blogger community for families dealing with autism. She has guides and references and etc to help families. Might be worth having a look at her blog. http://www.katesaysstuff.com she is also very very active on twitter.
felicakes recently posted..Today’s Fav…
Hi, you. Thanks a bunch for reminding me about Kate’s community. I follow her on Twitter. I will definitely take a look. xx
My middle child, who will be 11 on Sunday, used to act the exact same way…and we had no idea what to do. This was before he was even diagnosed with ANYTHING! But having an older child, I knew his behaviors and reactions were not “typical.” You are on the right track with the therapies. That was the best thing we ever did. He still has angry outbursts, but not nearly as much. With lots of therapies, he is able to articulate what is going on in his head and problem solve what to do about it. We work very closely on medication and he has been put on antidepressant and anti-psychotic meds and that has helped him a great deal. That doesn’t mean your son would need them…I just know how they have helped my son. I wish the best for you and your son. There will be rough days, but know that he is not doing this on purpose, it’s just the only way he knows how to handle it.
Meredith recently posted..Vintage Beach
Hi Meredith. Thanks for the kind words and hopeful things. I’m glad you dropped by, it’s great to meet others who have been there. xox
My son’s teachers described his tears as “My world is broken, why can’t you fix it?” Heartbreaking.
It does get better. It is only as I read posts such as yours I am transported back a decade to how it was. Different yet similar.
Are you on the Gold Coast?
E-mail me, I might be able to suggest some ideas.
Madmother recently posted..A Rehash: Rose-Coloured Glasses in the ASD World.
I just wanted to say that I understood a bit. My son has this primal, emotional cry and when I try to explain it to some people, they seem to think I just *feel* like he is in deep emotional pain because I am a doting mother.
Thank you. I wish the best for you and yours for 2013.