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Rachel Robertson 380x567 Confessions from a parent of an abnormal child.

Rachel

 

 

 

 

 

by RACHEL ROBERTSON

As the (proud) parent of an autistic child who is not “normal”, I want to respond to the article “Is my child normal?”  In this post mothers were invited to share their children’s unusual behaviour so that other mothers can reassure them that this behaviour is “normal”.  Over five hundred people posted a comment on this story within the first few days.

I think that sharing stories within a community is important and even healing.  What I do want to add though, is that I think the Mamamia community should also use this opportunity to spearhead a re-think about the concept of “normality”.

This would be a fantastic initiative because it would help those of us living with difference and disability to feel less excluded from mainstream society.  And I think it would also help all mothers feel more comfortable with how they and their children are expressing themselves.

There has always been a huge range of variation in all aspects of the human being (and other species too).  In the past, this variation was acknowledged and expected; only gods were perfect or ideal and humans were expected to exhibit variation.

As Lennard Davis has described, with the growth of scientific measurement and particularly the development of the normal or norm curve as a mapping tool, social scientists started describing something called “normal”.  This “normal” was basically those people who fell into the middle of the norm curve.  People on the outside edges became suddenly non-normal or “abnormal”.  A shift occurred where the norm was then amalgamated with the ideal to create “normality”, which then became not only expected but also preferred.

This has not been all bad, of course.  As a result of this shift, for example, we can now access charts which show typical child development.   These are helpful for parents and professionals.

But there have been negative results from this shift as well.  We no longer expect human variation.  People who fall outside the norm are often considered second class citizens, defined by their differences, usually by lack and deficit.  “Normal” has become a term of approval and abnormal a term of condemnation.  “Normal” behaviour and life is defended by setting up barriers against those who are abnormal.  No individual means to do this, but it is part of the structures of society.

I totally support the use of things like charts of typical child development.  If your child isn’t meeting some of those typical expected milestones, it is a good idea to seek some professional advice to make sure your child gets all the help she or he might need.

But should we really be talking about “normal”, or even typical, behaviours?  Should we start categorising unusual behaviours as too weird or different to be “normal”?  Doesn’t that suggest that some people are less acceptable and valued than others?  My son preferred reciting the times tables over singing or listening to nursery rhymes.  Yes, that’s unusual or atypical. Yes, it was an indication that he was autistic.  But does that preference make him “abnormal”?

How do you think a mother like me feels when I read that Mamamia mothers can reassure other mothers that their children are “normal”?  It sounds as though being the mother of a child who is different is sad or bad or not a part of ordinary life.  Yes, having a child with autism can be challenging and it is sad for me to witness his daily struggles.  But all motherhood comes with challenge and sadness.   I experience huge joy from my son, just like most mothers.   He is a funny, loving and lovable boy, who at almost thirteen is interested in girls, iPads, cooking and lego.

Please don’t mimic the medical and commercial world where sameness is good and difference is bad, because difference is always seen against a standard measuring tool of “normality”.

book cover 380x579 Confessions from a parent of an abnormal child.

Rachel’s book

Mamamia can be a forum for embracing difference and diversity, a space where those of us living differently can be respected and valued alongside those living more typical lives.

I fully appreciate that the intent of this post is to support mothers and I have no problem with it, nor with people sharing their stories and hearing other voices.  That is all good.  Being a mother right now is obviously tough – why that might be is another article, but if this initiative gives people some confidence in their own relationship with their kids, then that is terrific.

I just ask people to think more deeply about their notions of what is “normal” and why it is that we feel reassured when we are told our family is “normal”.  Difference and disability are frightening to people – I know, I’ve been there and seen the faces, including my own.  But it shouldn’t be.  It is a natural part of life, the planet and being human.  Please embrace it!

Rachel Robertson is the author of Reaching One Thousand: a story of love, motherhood and autism (Black Inc 2012) and a lecturer in writing at Curtin University. You can find her blog here.

Read a beautiful story on how a mother copes with her autistic son  our sister site iVillage.com.au here and also take a look at this  video – what autism means to you.

What does normal mean to you? 

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63 Comments so far

  1. afd

    I think normal means no more or less than the meaning that comes from the norm curve. I agree that the concept produces useful instruments such as charts of expected development.

    I also agree that it should not be a value judgement. As others have said, life would be pretty boring if *everyone* was ‘normal’.

    I also recall a few years ago reading a (possibly fictional) objection from a parent, upon reading ‘average’ on their child’s report. Their child was most certainly not average, thank you very much! :)

    I agree with that kind of sentiment. I’d say it is *probable* that most people are ‘abnormal’ in some aspect of their abilities or personality. It’s those things that make life interesting. Yes, the more extreme differences can present substantial challenges.

    This is related to the whole question of labels – good or bad? My opinion is very pragmatic on this point. If labels get you resources, great, use them! If they get you discrimination, exclusion and unhelpful ‘advice’, pretend they don’t exist. :)

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  2. Rachel Robertson

    Thanks for your comments, everyone! All really interesting.

    I must admit, I was taken aback by the title for my piece. I suggested “Deconstructing normality” – not very attractive, I guess, so no surprises it wasn’t used!

    BTW, I don’t think we should necessarily avoid using the terms normal and abnormal in daily life (though I myself prefer not to use them much). My suggestion is that we should re-consider our notions of what we mean by normality and the judgements we sometimes make on that basis.

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  3. Lisa

    Great article :)

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  4. the Original Camille

    we have finally got our house in order after the visit of friends and their 3.5 yo boy. It was like a visit from an d 18 month-old:

    He still wears nappies (although I realize this is still within norms).

    He played for about 5 minutes with a train set, then opened the toy cupboard and tipped out everything in each box.

    He went into our room and pulled everything off the bed.

    His speaks in mumbled, single words. This has their friends with similar-aged kids telling them to have him “checked out”.

    On his way out, he grabbed a vase of flowers and tipped it. Over a power-point. This short-circuited the house. When they left, we went next door to plug an extension cord into their power, so we would not lose all the food in the fridge.

    I think he needs early intervention, but his parents are too scared to find out he might not be ‘normal’, so we watch him lag further and further from his peers.

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    • colleen

      Oh my giddy aunt, Camille, I hope they can have him checked out. Not to hear something they don’t want to, but to give him every single available opportunity to live well. And so they are not isolated, as some of their friends will doubtless find visits too much to handle.

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    • Lora

      We also have friends who were in denial for at least 3 years that their child was ‘abnormal’ in any way. He never responded when people spoke to him, threw tantrums and would get upset by the strangest things. When they finally had him tested, it turned out he was autistic.

      I understand parents not wanting to admit any abnormality in their child, but I think it would be in the children’s best interest to diagnose any conditions early so they can get help earlier.

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  5. Faustino

    I am choosing personal blogs that contain really good information on what exactly is any way you like plus the ideal truck caps is certainly.. Faustino

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  6. Cath

    This world would be a very different and boring place without people who had the gift of Autism. People come in all shapes, sizes and abilities. Genius is often reserved for those on the Autism Spectrum.

    Can you imagine a world without Einsine? He was rumoured to be on the spectrum, so is Bill Gates.

    Then there is this, a man who drew the NYC skyline from memory after a 20 minute helicopter ride. http://www.dailymail.co.uk/news/article-1223790/Autistic-artist-draws-18ft-picture-New-York-skyline-memory.html also on the spectrum.

    I’ll say it again, the world would be a very boring place without the gift of Autism. Embrace our differences, there is no such thing as ‘normal’ anyway.

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  7. Mug

    I understand that having a disabled child can be so isolating that sometimes when people use a word (i.e. normal) it can feel like once again society is trying to pretend your disabled child is somehow not as important or worthy as the ‘normal’ children. As soon as I hear someone say the word ‘normal’ in relation to children I just mentally convert it to ‘mainstrean’ because that’s usually what they mean.

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  8. Anonymous

    Maybe we talk too much and over analyse.

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  9. AS

    As a child psychologist and parent I find when parents say “Is this normal?” they mean “should I worry about this?”. It’s a good question in my view as a starting point for getting kids and parents the help they need.

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  10. Anonymous

    I’m surprised at how many people take offence at the word “normal”. There is no such thing as “normal” BUT to me in this context, “normal” would equate to “majority” and the majority of people don’t have an intellectual impairment/disability.

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    • Anonymous 2

      Hi Anonymous, I’m not sure if you’re referring to autism as an intellectual impairment/intellectual disability, but just for the record autism is NOT an intellectual disability, it’s a neurological developmental disorder. However, kids with autism do sometimes have a intellectual disability as well, just to confuse things! Thanks.

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      • Anonymous

        My comment wasn’t about autism. My brother has autism and Down Syndrome so I’m aware of what it is ect. He is low functioning and non verbal. My comment was more about in general, especially with disabilities that do include an element of intellectual impairment.

        I think all parents have an element of “doubt” about their own childs development.

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  11. Michelle

    Thank you Rachel for this article. I couldn’t agree more!!! I am the proud Mum of three gorgeous young adults (22, 19, 17yrs) and two of them are on the Autism spectrum. Life has been extroadinarily challenging, tough at times, joyful, sad at times, ALWAYS interesting and not what could ever be called “normal.”
    I came to terms with that a very long time ago and I am more than happy with our life as it is. It’s pretty amazing and “normal” is boring. :)

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  12. Napoleon

    My heart breaks for any child born with special needs, and the incredibly difficult path trodden by those parents. But this seems hyper-sensitive to me, and frankly reeks of political correctness. I love MM because it is all about how women talk amongst themselves, and a “is this normal when my child…” is the most typical of conversations amongst parents. It’s not a conversation i might have in front of a friend with autistic children, we would have a different conversation about chilod behaviours. so on this forum perhaps you should dip in and out of those conversations which suit you, not try and regulate how everyone else is allowed to speak.

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    • Michelle

      I don’t think that’s what Rachel is trying to do, and I am talking as a Mum of autistic kids. She is just trying to get us to embrace our differences, the incredible variations of human behaviours and not get so hung up on “normal”.
      Life is so much richer when you do! :)

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    • angie

      napoleon, parents usually don’t want sympathy, just some understanding and acceptance, so don’t break your heart…

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    • Anonymous

      I agree, Napoleon. I had the same response when I read the op-ed.

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  13. Lou

    To me autism is my ‘normal’. My typical child, well he’s my ‘broken’ one! My first child has autism so it’s all I knew for 3.5 yrs. when my little one came along I couldn’t believe the things he does- bucket on head banging into a wall, not wanting to eat properly, oh and the 2 yr old tantrums! We’re not sensitive to the word normal so unless someone says it in a mean way I’m not going to take offense- its a word we all use. Autism is my ‘normal’. Everyone (adults and kids) has a different normal, if everyone one was the same the world would be very boring! :)

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    • Mum of 2

      LOL Lou, I so understand this! I am still trying to wrap my head around my second child!

      It’s little things like the fact that my oldest has SPD so they don’t feel sensation like the rest of us (eg when they had a raging case of tonsilitis they didn’t even feel a sore throat. On the way out of the Drs, when the Dr had actually let me have a look in their mouth and showed me what should have been an terribly sore throat I said to the child ‘The Dr said you probably have quite a sore throat – are you sure it doesn’t feel sore?’ and the response was ‘oh, it is just a LITTLE sore’…!!). For this child to report that something hurts means that something is very very wrong. That’s why it does my head in when my second child will report a headache, or sick tummy – I am used to this meaning that things are almost catastrophic! I still have to rein myself in every time and think before I react. Prior to my second child I guess I had just started to think that kids don’t feel things the same way adults do (because I had no experience otherwise), so it has been a shock to the system to find out differently and not over react every time the little one says they feel unwell! There are so many other things that I could describe where ‘not typical’ was my ‘normality’ and now ‘normal’ just feels weird and is taking just as big an adjustment for me to run the two worlds side by side at the same time! :-)

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  14. Daisy

    Mamamia, I know from other articles that the person who writes the article is not the author of the headline. It detracts horribly from your column when you write this sensationalist, Current Affair/New Idea rubbish as headline.
    Rachel, I enjoyed your post.

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    • jamilarizvi

      Hi Daisy

      We’ve used quotation marks around the word ‘abnormal’, just as the author has herself when she described her child as not ‘normal’. The whole article is about the subjective view we have of the word normal and how it has different associations for different people.

      We’ve used the quotation marks to signify that we don’t necessarily agree with the label but it is one that is used all the same. I note further down in the comments that one parent of an autistic child was defending the headline as appropriate so I’m comfortable leaving it as is for now.

      Thanks for your comment.

      Cheers,

      Jamia.

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      • Daisy

        Ok. I accept that you know more about this stuff than me! I just felt it detracted from the intelligence of the post. :-)

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    • Anonymous

      I agree Daisy, something has changed with the headlines to be very “Today Tonight”

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  15. Ash

    If I recall, the original article was a light hearted way for parents to be re assured that they shouldn’t worry about their 3 year old eating crayons (or whatever, I’m not a parent – so I made that up :-) ). Maybe I am just feeling too cynical today, and sorry for being cranky, but the above reeks of a person who has written a book drawing a long bow to find a publicity opportunity.

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    • Parent

      I agree – you are being too cynical today.

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  16. CBR

    I’m at odds with this, mostly because of this sentence:

    “Please don’t mimic the medical and commercial world where sameness is good and difference is bad, because difference is always seen against a standard measuring tool of “normality”.

    Well.. normality or abnormality doesn’t naturally imply goodness or badness, which are constructivist concepts. Normality and abnormality are quantitative, statistical concepts: deviation or aberration from the “norm” is a descriptive, not a prescriptive concept.

    It snowed in Canberra yesterday, if only for a few minutes in a few isolated areas, and such an event is certainly a deviation from the normal: it is abnormal. But that doesn’t mean it’s bad, or wrong. Abnormal behaviours aren’t bad, or wrong. They just are.

    Perhaps in the search for meaning over disability we have become oversensitised to the natural, mathematical concepts of normality and abnormality. Abnormal behaviours, such as those displayed by individuals on the autistic spectrum, are such by definition. But that doesn’t mean they’re bad. Merely not within a standard deviation from the mean.

    EDIT: I suppose I should address the thesis of the article which is that people are disturbed (in the dictionary definition of the term) by abnormal behaviours because they are abnormal, and thus somehow wrong. I don’t refute or excuse this. Identification of abnormality is not something we’re ever going to be able to suppress, given its evolutionary imperative. I went out with someone who was high-functioning Aspergic and had ADHD to boot, and his behaviour did occasionally disturb and frustrate me because it WAS abnormal – abnormal, but not wrong or bad. I wasn’t sure how to deal with it, and you know what? That’s okay.

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    • Anon

      Great comment

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    • Anonymous

      Oh I’m so glad you wrote this, the word normal is not inherently bad! In fact without the concepts of normal, like normal or typical behaviors at specific ages, people who might need assistance would fall through the cracks. People should not be scared of the word normal but linking normal and bad together is a problem. And science and medicine are not the problem here, societies fears of abnormality is the problem, fix the fear and no one would care if they were normal or abnormal!

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    • Mabol

      Hi CBR,

      I guess the issue here is that the semantics of the word ‘abnormal’ extend beyond the strict statistical definition. I feel that the author’s intention is more to challenge the perceptions and how we see and treat people that fall outside of the norm rather than to deny that they are not different in some ways from the strict mathematical norm.

      She does state that is is helpful in some ways to understand difference so that we may support and help people where it is needed.

      However I feel her main point is how we perceive and treat difference – rather than to deny it altogether.

      Its interesting that you bring up evolutionary science – Seeing that the basis of selection is difference. Difference and diversity ‘is’ normal if not the ‘norm’. Because what may be a statistical outlier may become the adaptation and then the norm in a changing environment. The norm itself is relative. Relative to culture and time and experience.

      Honestly I think there is something of human experience that can not be captured in propositions and analysed statistically. If the growth of the scientific analysis of human experience is so accurate and powerful – why is it that so called mental health issues such as depression are increasing not decreasing. Even in societies which are materially wealthy and have access to this knowledge and the support structures involved?

      What is the cause of this? I’m a huge advocate of science and technology but I think that this needs to be tempered with a wisdom that we don’t always have. The foundations of human experience lies in worth – what is the equation for that? There is a poetry to human experience that escapes logical and mathematical expression.

      Difference is normal if not the ‘norm’. It may be confronting and difficult for some but it is normal.

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  17. vanessayoung

    People are too casual about language. We have a child with autism in our family, we NEVER say or think normal and abnormal, we do say “our kids do…… where a TYPICAL child would do something else”. I am currently fighting to have what is casually called “The Disability Unit” at my granddaughter’s school to be called something else.
    The other thing that really bugs me is that people who have typical kids do not seem to realise that our kids are as loved and valued in our family as their kids are in their families. There is so much casual cruelty in the world: a family member delights in calling me to celebrate her granddaughter’s achievements and always follows it with “I feel sorry that you will never see Chloe dance, act in a school play, play netball etc”. Grrrrr!

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    • Michelle

      Vanessa, tell your family member to take a running jump!! She has no way of knowing what Chloe can achieve!! Our kids can achieve incredible things,more than they are given credit for. She will surprise everyone

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  18. LBD

    good article but I agree the title is in contrast to the whole point of the article

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  19. Bex

    This was a good article but the title is shocking and offensive. Kids, or anyone with special needs are labelled often enough but to be refered to as abnormal is degrading.

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    • Tripitaka

      I agree. Also, she’s not ‘confessing’ anything – a word which makes us think she’s done something bad, when actually she hasn’t.

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    • justine

      Thus the reason for the use of quotation marks around the word. The sense of irony was not lost on this Mum of a beautiful child with autism.

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  20. Anon

    What a great article. However I would like to add that when discussing falling outside the range of ‘normal’ you have only discussed possible ‘deficits’. As a parent who raised a child classed as very ‘intellectually gifted’ (who is now an adult) it was an extremely hard road. Anyone who falls outside the ‘normal’ range is faced with all sorts of difficulties.

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    • Mum of 2 cheeky monkeys

      Thanks for your comment, I am going through that right now. It can be really really hard – heartbreaking sometimes. There are very few people I can talk to about it as most people think, ‘poor you, you have a smart kid!’ But its hard, especially when he is in public. You just want everything to be perfect for them

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  21. Parent

    Thank you Rachel for speaking up for those of us with “different” children. And thank you to mamamia for recognising the need to post an alternative view to the “is my child normal?” piece. I know that the original article was not meant to offend but unfortunately those of us with “different” kids tend to be quite sensitive about these matters, probably due to the alienation we already feel.

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  22. Luc

    Beautiful post, thank you.

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  23. Aerin

    My son would be classified by society as “normal”. But as a very young child he was quite unusual and I often wondered if there was something “wrong” with him. It turns out, the problem was not with him, but with me – and my lack of understanding about individuality. His older brother (4 yrs older) was a text book baby and for some reason I assumed that any children who followed would be the same. I was pulled up by his paediatrician who rightly said to me “you know it’s ok for him to be different to his brother”. I more I accepted their chalk-and-cheese constitutions the better it was. The same doctor said to me more recently “we all tell our loud child to be quieter, the quiet child to speak up more etc – we need to just let them be who they are and love them for their uniqueness”.
    The word “normal” is probably not relevant given the vastness of human differences. I think it’s important to recognise certain deficits in order to maximise support – but not to classify or create minorities – this threatens to imply that the deficit or the disorder is the the defining characteristic of a person, which is never is.

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    • Lynnie

      I am totally where you were!! Great advice :)

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  24. Anon

    Thanks for writing this thought provoking piece and opening a discussion for people to share experiences that may be difficult to share with the usual mothers groups etc.

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  25. Freyja

    My oldest son was a bit different as a young child. He wasnt diagnosed with anything and I refused to test him as I loved his unique personality and he wasnt suffering socially, just spoke his mind a little too often at school and was reluctant to work if it was ‘boring’. He’s still like that at high school. I know some kids have definite learning and social difficulties, but I do think kids tend to be over diagnosed at ages where they are still sorting out their own personalities and who they are. His brothers a bit the same, but still nothing wrong with him, just not average. So what? Neither is their mother. :-)

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  26. Aly

    Thank you for this article.

    As a mum to an “abnormal”child – he has ocular albinism meaning he will likely be legally blind (but still able to see – but not able to drive or do other activities that need good vision).
    My little guy doesn’t walk yet at 14 months – his poor vision makes balancing etc more difficult. His eyes look as though they are constantly “searching”.

    THe lack of visual input means he displays “abnormal” behaviours such as rocking to increase the stimulation he gets from the world.

    It can be hard being at my mothers group (who are all fantabulous women and lovely kids) simply because you can see where you don’t fit in to the “normal” world.

    I love my little guy to the moon and back and in my eyes he’s just my little man but it does sting from time to time to know the struggles he may face and the fact that he may seem different.

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  27. Anonymous

    I understand the idea of classifying “normal” from a medical pespective but in society, as a community, who are we to judge what is normal? Our idea of normal is subjective, it changes from person to person. Just because someone doesnt tick all the “normal”, median or average boxes, why should they be cast as “abnormal” or different? We are all on the same spectum. The idea of being normal or the concept of normailty should be left in the doctors office and not brought into society.

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  28. Mum of 2 cheeky monkeys

    That is really a beautiful article

    My son is not considered normal either- although his behavioral issues are nothing like all the issues parents of autistic children face. He has had a tough year at kindi, and was always in trouble. He started pushing other kids around, throwing tantrums- lots of the normal 2 year old stuff, but more serious and to a whole different level. Last week he jumped on his friends head. When we asked him why he says he is a superhero doing a loop de loop trying to save his friend from an evil enemy! The kindi had a psychologist look at him because they didn’t know how to handle him. She had a lot of great suggestions and has helped a lot. She thinks he is actually gifted and talented but has very low social skills, which is actually a common behavioral trait of g&t children. So I suppose it’s good news but right now it’s terribly challenging. He just isn’t like the other kids. I can’t take him to the park, I get nervous every time I pick him up from kindi because I know what the response will be when I ask how he’s been and I worry about him a few years down the track. They want us to get a toddler iq done, so they know what they’re dealing with because sometimes these kids really struggle with school work. I can’t really talk to my mum friends because as soon as I say gifted and talented they think I’m bragging.

    So for me normal parenting would Be going to the park without worrying he would injure another child or picking him up from kindi without a teacher conference. I love him to bits and want him to be happy and the best he can be, and I wish I didn’t have to worry about him do much.

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  29. clarinette

    I’m not normal , since i have asperger’s, my son is diagnosed as PDD-nos, so “autistic but I can’t be arsed to refine the diagnosis” type. It’s always nice to witness the level of acceptance there is in english-speaking countries about autism , I was unlucky enough to be born in France, and so is my son. We’re still waiting for autism to be recognized as a neurodevelopmental disability (they think it’s a psychosis here, cue nightmarish journey). Thankfully awareness of our situation is coming, soon, we hope. http://www.shamefuldocumentary.com/about.html

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    • Mum of 2

      Holy cow clarinette! You have gobsmacked me with this one – in France they seriously consider it a psychosis??

      Wow. The professionals over there seriously need an education. So they obviously don’t agree with the five areas of difficulty then and believe it is pretty much just one or two, and they are all mental issues? (I mean the first three, and the others they are now discussing of sensory difficulties, and motor as being likely part of it all). Geez! They obviously haven’t lived with someone for whom it is just the way they are wired up then have they!

      I hope that things change over there sooner rather than later.

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      • clarinette

        Hey :) yes, a psychosis. Due to the mother’s either “death wish on the unborn child” or smothering/incestuous thoughts about the newborn” (very hard to debunk since mothers of autistic kids in france easily become over-protective and defensive, seeing the attacks they and their children have to fight against)….and social services are often called on, a huge amount of children are being forcefully placed in psychiatric hospitals (after being removed from their “toxic” parent’s homes, for “default of care”, since the parents are starting to refuse psychoanalysis as a cure for the whole family, now that knowledge about what autism really is has started to reach us through the internet. it is really bad…..thanks for caring enough to reply, we’re hoping for interventions from other countries, things won’t change from the inside, we learn freud in high school here. As fact.

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        • Ali Flint

          Clarinette I am another gobsmacked by your news. It’s fantastic that this forum can gather the kind of useful information which you have profered us. It is astonishing that France teaches its youngsters Freud. Here in Australia, at a high academic level, Freud is almost unanimously debunked these days. It is due to him that the dreadful nonsense of which you remind us is still perpetuated. And due to him also that we mothers (and fathers also, or course) are still blamed for the “malfunction” of our children, as if everything in the child’s life was somehow under the control of our own unimaginable personal power!

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          • clarinette

            It’s heartwarming to feel some people do care :) for anyone interested,check this new york times article about a documentary that revealed the issue and was banned in France. http://www.nytimes.com/2012/01/20/health/film-about-treatment-of-autism-strongly-criticized-in-france.html?pagewanted=all

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            • Faybian

              What a surprise, they don’t believe in ADHD either.

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            • clarinette

              nope :p my son is also ADHD, I mentioned his inability to focus and stop moving to the psychiatrist, he told me “how curious, it never happens in my office, that should be a clue as to what the cause is, to you, shouldn’t it?” (with a snide smile, as in “the cause is you, lady. don’t even ask for meds or I call CPS”. Ok……..)

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            • iNerd

              clarinette – re: post below. You should take discreet video of your child’s ADHD behaviour when in their typical environment. That way way the psychiatrist can see with his/her own eyes the truth of the situation. Kids never act like themselves in a strange environment, or around people they do not know/or well.

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            • Lucinda

              Clarinette, if your son does not display ADHD behaviour in front of the psychiatrist then he does not have ADHD, believe me. Children with ADHD cannot focus, or often sit still, for any length of time no matter where they are. How is he at school? It may upset you to hear it, but ADHD does not discriminate depending on the child’s environment. If he is only displaying poor behaviour at home then maybe that is a clue?

              I understand your son already has a diagnosis of PDD – children with pervasive development disorders will often display some symptoms like ADHD, but usually it is not ADHD on it’s own, and it is not all the time. It’s also not something they will often prescribe ADHD medication for either.

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            • Faybian

              Beg to differ Lucinda. Every child is different and given the differences inherent in the ADHD diagnosis (impulsivity, in attentiveness, hyperactivity). Some children may be affected more than others.
              My son was diagnosed with ADHD and impulsivity was and still is his biggest issue, as well as inattention. he did not overtly display any stereotypical ADHD behaviour for nearly a year at his paediatricians.
              I could see some impulsivity in his non diagnosable/diagnosed sister, but she coped far better with school far better than her brother.
              Yes, there can be some confusion with symptoms of an ASD and ADHD and I see where you’re coming from, but it can take time and more than one mental health professional to get a clear, final diagnosis.

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  30. Jem

    My new normal…my 12yr old daughter falling in a heap…panic attacks and overwhelming anxiety…school refusal…school counsellor…psychologist…psychiatrist…and finally…a diagnosis of Aspergers…3 yrs later…I am still trying to make sense of it…what did I miss…how did I not know…

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    • Mum of 2

      Oh Jem, big hugs. I know what that feeling is – to wonder ‘what if’ to a whole lot of things that you did in the past regarding your child. My mantra which helps me with that one is “I did the best I could with the information that I had at the time”. No one can ever be asked to do more than that. It is not humanly possible. We can wonder what we would have done had we had a crystal ball into the future, but we truly can’t change the past, and we did the best we could with the information we had at the time.

      Say it with me…! You did the best you could with the information you had at the time. Now your only choice is to go forward from here, and do the best you can with the information you now have. Hugs hun!!

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    • Woolly

      Jem, you didn’t miss anything, your a wonderful mother, don’t beat yourself up as I’m sure you’ve done the best you can. My son was recently diagnosed and it was four years of asking for help from health professionals, but they couldn’t give us answers. So much more needs to be done in the community and with health professionals. Autism is still very misunderstood by the “normal” population. We love our son, he is quirky and different and brings so much joy to our life. We need diversity, the world is a much better place for it.

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  31. Urban Fringe

    Thank-you for writing this piece – with a beautifully and sensitively conveyed message – and healing too for all us parents who have children with disabilities or delays. I too was a little gutted by the piece on ‘normal’ behaviors in children (although I knew it wasn’t necessarily Mamamia’s aim to exclude or denigrate) – so nice to have this piece published to lend some balance and added context on the debate on so-called ‘normalcy’ in children. Although I believe in the absolute primacy of professional, medical support and expertise when it comes to helping our children, sometimes the greatest emotional and philosophical wisdom comes from other parents on a similar journey.

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  32. theboysmum

    This is a great article, my nephew has a dual diagnosis of autism as well as integrated sensory disorder. He is not considered normal by the majority of people but his family and those close to him love him, support him and embrace him. He may not be considered normal by society but his behavior, moods and personality are what I consider, his normal.
    I believe that every child is different and therefore each child has their own version of normal.

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