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autism 1 380x380 The reality of Autism

Hannah's brother

There is a certain silence to Autism.

Not in the raging meltdowns my brother will have that wake the neighbourhood at 5 a.m., but in the way the progression of the disability puts glass walls around not only the autistic individual but also the family that journey with the sufferer. Autism is an isolating disability.

Perhaps it is in the unpredictability of the condition or the difficulty to comprehend just what exactly it is, but I see such muted frustration in my parents when they are asked how life with my brother is going – they can only reply with ‘oh, it’s been a difficult week.’ And this euphemistic reaction is the most blatant understatement; instead, they should reply with, ‘well, my son has been swearing like a sailor all of a sudden and needs restraining when he tries to kick in the walls in the middle of the night. And then he heartbreakingly weeps at the difficulty of his life.’

It seems like there is no grid for people’s understanding so my parents smile gritted smiles and tone down the truth. What makes it worse, though, is that their frustration is nothing compared to the internal torment that a person with autism feels daily. To find my brother sobbing in his bedroom because life is so hard makes our own struggle muted; we can’t find words for a feeling he has no words for – it’s just hard and so becomes hard for us to express.

To be honest, it is difficult to understand exactly what Autism’s reality is without living in the storm of it, but I am calling for a desire in people to understand and support.

‘Autism’ has been a bit of a catchphrase in recent years (indeed, someone I know recently stated ‘well, everyone’s Autistic these days’ – suppress rage here). Heightened diagnosis and publicity has encouraged society to acknowledge Autism’s presence in greater depths. There are many educational provisions for smaller children that are outstanding, but we are venturing into seemingly unchartered territory when the children that had pioneered the early intervention movement start to scope the scary terrain that is adulthood.  That is where it gets confusing. That is where delayed teenage rebellion and angst mixed with the fear and disorientation of autism gets overwhelming.

autism 2 380x285 The reality of Autism

Hannah with her brother

There is no straightforward map to this condition. There aren’t really any signposts or predictable behaviours. There is no growing out of it or getting over it.

Every individual has their own struggles and obsessions, fears and rages. What I do know is that there can be an alarming misunderstanding of the Autism Spectrum Disorder and the precious people that struggle with it.

Just this week my mother took my brother to do the grocery shopping. As she shopped he stood out the front talking to himself, rocking his torso to and fro and taking photos on his iPod of the world around him – that’s just his thing at the moment. Mum came out, laden with bags, to be called out to by a P-plater in a red Ute, waiting for his mate in the bottle-o nearby: ‘hey lady!’ Confused, she neared his car, to be told ‘you better be really careful of that bloke over there. He’s stalking you, watching you all the time … he’s taking photos. There’s something wrong with him – he looks really weird!’ My mother, stunned and shaking with rage, went over to his open window and said: ‘that ‘bloke’ is my son. He has autism. There is nothing WRONG with him; he is NOT weird. He has a major disability. You are obviously quite uneducated and completely ignorant to jump to so many wrong conclusions!’ She spent that afternoon torn between the rage and grief that comes from the fact that someone who appears different can easily receive such judgement and intolerance.

So I write this without any particular agenda or campaign. I just want to break the silence that has muted my brother all these years and ask for people to at least attempt to understand the beauty and horror that is living with Autism – the individuals that suffer from it deserve that respect.

Hannah Macauley-Gierhart is a writer, English teacher, new-wife and insatiable tea lover. You can follow her on twitter here.

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58 Comments so far

  1. Bex

    What a beautiful article Hannah. I have worked with Tom and have seen the good side. We have had wonderful conversations about the AFL and sea creatures as we walked a long the beaches. I always liked how he sought more information. Your article does the same thing in seeking to out the information about autism out there.

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  2. Marn

    It’s always strangely nice to know I am not the only one who deals with these same issues. My son is 10 years old and has Asperger’s syndrome. Lately he has become very aggressive and disruptive. It’s hard on his 13 year old sister to cope with and that hurts. I can see the pain my son has inside and the sadness he carries as he struggles to make friends or behave ‘normal’ in social situations. I don’t wonder why he is my child or get upset that I may probably never do many of the things I planned to do with my life. I love my son. He taught me more than any other person or book. Good luck to all who ride this roller coaster! Just never stop believing…

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    • Amber

      Thank you Marn. You have touched on so many issues I face. My son is 8 and autistic. He struggles to make friends and deliberately avoids social outings (the school disco was something he definitely did not want to attend). I sometimes feel sad but I realise he is my gift to believe in tolerance and understand we are all different in this society.

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  3. Ariel

    Onya for writing about this. Have you read Kathy Lette’s Book The Boy who fell to earth? it’s based on her experiences with her own autistic son and at least got the topic OUT!!. But as you there is a huge spectrum – my brother had it but he was also very much intellectually disabled and may have had brain damage from a fall. In those days 50s-60s very little was known about the whole thing and a lot of blame fell on my Mum etc etc but the worry is that we haven’t made a lot of progress as a society in understanding

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  4. Anon for this

    Hannah, with all due respect (and I do respect you for writing such a moving piece, for being an advocate and for being such an obviously great sister), I can understand where the ‘p-plater in the red ute’ was coming from. A strange man standing outside taking pictures? That would freak out any lone woman. And yes, your brother has autism, but I (and the p-plater) don’t know that. Your mother’s response could have been educative rather any snide–there’s nothing to be angry about. As you yourself have said, there is a lack of knowledge in the community. And sure, your mother is right, he was completely uneducated, but that’s not his fault. And that response probably didn’t help.

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  5. Stephanie

    I love you, Han. Your words are powerful and your story can cause change. I hope that, this month, people actually take the opportunity to get educated, to open up their minds and learn to not be afraid of what they do not yet understand.

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  6. Phil godden

    Thanks. Thanks Hannah.

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  7. Disability advocate

    Wonderful post. Unfortunately there is a lack of understanding and silence about all sorts of disabilities. Having been able-bodied for the first part of my life the contrast is extreme.

    Disability (be it autism or something else) seems to bother ‘other people’ more than it bothers us!

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  8. staceyanne

    thank you hannah for your story…my 17 yr old son is autisic and the teen years have been tougher than when he was younger… he has smashed all my furniture{except two couches}, i sleep on two matresses on the ground in my room as he lifted up and smashed my queensize bed, im saving for my third washing machine as he has been known to lift them up and smash against walls…the police have been called to our home many times in past two years my neighbours due to his rages, at first they couldnt believe he could be strong enough to do the damage he has done, but they soon believed…its like during his rages he turns into ‘the hulk’…
    puberty hasnt helped either as he thinks thats just something else wrong with him and that sets him off too..
    i miss my kind, thoughtful young man [i know he is still there, i just havent seen him since my son started high school]…that young man used to bring me flowers when ever he went shopping with his nanna…

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  9. teacher 16 years

    Hannah, thank-you so much for your article. As an early childhood teacher who is in the long slow process of studying for a masters in special needs education, it helped me to think ‘outside the box’ and realise that even if there is intevention in the early years, we still need to consider what will happen after these beautiful children leave the confines of our schools.

    What is the answer? I am still trying to figure it out. But I do know that since beginning to teach 16 years ago, I have seen a rise in the number of children diagnosed or in the process of being diagnosed in a ‘normal’ classroom.

    There is an elephant in the room in relation to autism and the autistic spectrum that I, as a teacher and parent find difficult to address, but here goes. I have taught Autistic children, from one end of the spectrum to the other. It is very difficult, but rewarding. The thing that always worried me, however, (and this was not the fault of the child, or their parents) was the time taken away from the other 29 children (lets not kid ourselves here, most class sizes are around this now, even in early childhood). I have NEVER had a full time aide, even teaching prep. When handling difficult situations (tantrums, chair throwing, kicking, punching, etc) that are the by product of frustration caused by their condition, the other 29 children had to watch until we could get someone else into the room. Please, please, please, can we have some more funding so that EVERYONE can have access to an education they deserve.
    Sorry, I’ll get off my soapbox now. Thanks again Hannah. Love to your mum and dad and especially your brother xx

    We live in a prosperous, wonderful country. Surely you shouldnt have to be a millionaire to get help for your child when they need it.
    Ok, I’ll get off my soapbox now.

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  10. Miss Brown @ missbrownspeaking

    Good on you Hannah for giving a small insight into what it is like having a family member with autism. My best friends son is autistic, and we often witness the difficult and unpredictable behaviours he exhibits. You are right, there is no getting over it or growing out of it, and unfortunately for my dear friend it’s just the beginning of a long hard road. In many ways it will probably get harder for her as he grows bigger and stronger.

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  11. N1col3

    Please please please can we have an article written by someone who has AS. I’m not criticising this article at all, it was beautifully written but I’m just tired of hearing about all the poor parents and carers who have a horrible life because they look after someone on the spectrum! Lets celebrate how awesome and diverse we are and learn about AS from the people who actually have it!

    Wendy Lawson and Rudy Simone are two excellent examples of women who have AS who are amazing to listen to – lets learn about it right from the source and not second hand accounts :)

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    • Daisy

      Many, many people with autism can’t read and write. They can’t even speak. Their carer’s need to be heard too, not just for a whinge. This is about raising awareness and understanding. Having a child anywhere on the spectrum is hard and has to be one of the hardest roads to travel. For many people there is nothing awesome about it at all. I appreciate your positive outlook but it grates a bit to read this comment.

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      • Mum2Adelaide

        Totally agree with you Daisy.
        Thanks Hannah for your story and raising awareness.

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  12. Adult Living with Asperger's

    I was diagnosed with Asperger’s at the age of 25 when I was in a rehab facility for a drug and alcohol problem.

    It answered so many questions for me and opened up doors for me. I always say I’m not disabled but I live with it. And I do, everyday.

    People are very naive. I have very few friends mainly through uneducated idiots who think that to settle a rage, or panic attack it’s ok to degrade me to the most minute form.

    People say there’s too much drama or that I talk bullshit about the fact that my father passed away shortly after I was diagnosed or a routine was broken when one of my friends moved interstate.

    I was told to “grow up” once during an anxiety attack at a football match. Only because there was a lot of people trying to exit at the same time

    My all time favourite would be when an ex friend tried to pick a fight with me with about 500 people watching and an well known football team was watching. 

    I was only so glad that someone who I do class as a friend came and stuck up for me and enquired nastily if she had a problem with me. Thankfully she stormed off and I haven’t spoken to her since.

    The ones who I do class as friends have either been there, or have done their research. And so patient with me during a bad moment.

     I thank them for it.

    It was quite reliving to hear that one of my now good friends is a special needs teacher, she said to me one day about how that when people are misinformed they don’t know what it’s really like for me. 

    I have a beautiful partner who is my hero who is so understanding with what’s going on or when she can expect a meltdown to happen.

    I recently went to New Zealand by myself and had a great time. 

    The general public aren’t so kind as well. I took the big step to live by myself and so on, I have done very well however there are the morons who try to stick barbs into you thinking I’m stupid or something.

    Actually no, I’m extremely intelligent and study a masters degree in Visual Arts at University where I get distinction marks across the board. 

    I always say to people that just because I live with a disability it doesn’t mean any different to me.

    Having done a few jobs in retail, there are customers who have resorted me to tears, couldn’t appreciate an apology after I took a little too long to read a voucher, been asked to leave with a police escort after he threatened me with violence and my favourite asked to shop elsewhere because of the way they have spoken to me or treated me.

    It really irritates me when people either, ask me if I’m “stupid” or treat me like I’m stupid.

    I don’t need to get to the level they’re on to understand what they want. 

    I am entitled to a job just like anyone else. What gives you the right to abuse me for something I live with everyday? 

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    • N1col3

      Big luvs to ya!!

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    • lovelifexox

      Hi
      My son has aspergers, he has major ability no disabilty, Aspergers has major positives, we just need to implement strategies for the social struggles. We have all benefited greatly from early intervention. He acknowledges that he is different from the ‘average’ being, and endeavours to remain really positive about it. I think all adults need to have a strong understanding of other beings, as well as strategies to deal with situations. No mental condition should be used to justify peoples behaviours, we all need to realise that the people we are upset with may also have major struggles or ‘disabilities’ they are living with too

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  13. Just a Thought

    Really lovely story, Hannah. It certainly can be maddening and beautiful, all at the same time. Your mum and dad sound like amazingly strong people.

    That being said, I realise that the guy in the ute misunderstood the situation, which would obviously have been distressing for your mum, and I understand why she educated him on what was actually happening – but I must say, if it’s a choice between someone speaking up out of concern for my safety or saying nothing in case they offend … I know which one I’d pick – just in case!

    This has actually happened to me before with my autistic uncle, and I simply, calmly, thanked the lady for her concern – after all, she meant well – but filled her in on the real situation. We ended up having a great chat about autism and it turned out she has an autistic grandson she loved to bits – so there was clearly no prejudice against people ‘on the spectrum’, just an overriding concern for a younger girl.

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    • alyssakt

      I thought the same thing. If I noticed someone was watching someone who they hadn’t made any contact with to let me know they knew each other, I’d keep an eye on them too.
      If he really said it in the way described, then he relayed it wrong.

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    • Lu

      I agree. My friends dad has alzheimers and had a similar situation out in public. He does behave strangely and it can make people concerned. Her mum presented the concerned bystander with the alzheimers card to explain the situation. I dont think people should be chastised for trying to do what they think is helping an innocent person from what they think could be a dangerous sitation.

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    • Ames

      I agree. Sounds like the bystander was just trying to be helpful and actually a good citizen by caring for the safety of a stranger. How are they supposed to know the two people are related and one is autistic?!? Expect much? I think a simple clarification and thanks for your concern would have sufficed and not put this person off potentially helping others in the future.

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  14. Lisa king

    Sigh …. First of all .. Anon for this ( above ) RESPECT for your post .. I can’t help but lol becsuse I know exactly what your talking about my son does the same .. Not funny by any means except that if you don’t laugh at times you will probably feel like your going to die. My son is the most wonderful , creative , intelligent , affectionate , kind , honest , loving , obsessive , impatient , confused , disconnected , loud , hurtful , but simply wonderful little boy . The rollercoaster that is his life and ours is one filled with joy and pain .. The hardest part .. The confusion his little brother feels , being ignored .. And seeing his brother treated differently.
    In regards to the ignorance of people .. When at work the other night a lady came to me and said watch out for that guy he looks like a weirdo and he’s staring , I replyed he has Autisum .. She was clearly embarraced but afraid to admit she said well how was I supposed to know .. We arnt asking you to know , but to be AWARE and think before you speak that it could be a possibilty !!!
    Bless you all x

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  15. Ari

    It really sucks that the p-plater mistook your brother so badly, but poor guy! He wasn’t trying to be disrespectful or cruel. He was showing concern (in an ill guided way) for your mother and he had the courage to speak out. I have been saved by a stranger calling out in a similar situation (obviously not from an autistic person!) And the poor guy gets abused. Next time I’m about to be beaten by an out of his senses drug addict and nobody calls out to see if I’m ok, maybe I’ll wonder if they’re just to scared they might offend me by mistaking the situation.

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  16. rainbow

    thank-you for sharing your story and hats off to your mum for giving that bloke a talking to. he’ll never make that same mistake again, well hopefully anyway.

    we have quite a few children at my boys’ school with autism. i see their parent’s struggling at times, and really feel for them. things like sports carnivals and excursions are so hard for them and such an added burden for the parents, but i am sure being in mainstream schooling is better in the longer term.

    all the best to you and your family x

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  17. Christine

    Thank you for sharing your story. I work at a specialist school and work with many students with Autism. Although there are times when both the student and I struggle (behavioral issues, communication breakdowns), I really enjoy their company and watching them progress.

    I have a younger sister with a language disorder, and it upsets me how there are a lot of ignorance and lack of understanding.

    Best wishes to you and your family

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  18. Lou deibe

    What a privilege to know you, and now to know a little about your family too!

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  19. tresa

    My heart goes out to you Hannah and your family especially your brother. I personally have been through similar, but as a parent, as my son is autistic and we finally got a break through on medication that has seriously assisted him in controlling his agression. I love to have contact with you and discuss this further please email me and I wish you all the best it is a long hard road but many travel similar with you. My life has evolved around my son and many of my happiest moments and my darkest times have been relating to him but I would never have it any other way. We love him with all our hearts and pray one day they will find a cure.Thank you for sharing your story and in our journey I have come across many disturbing people with no understanding but also it brings out the best in the majority of people which touches me deeply.

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  20. Jenn

    Also, I’m sick of people asking me if I would change my brother to be ‘normal’. I am proud of my brother and would not change him for anything in the world.

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  21. Jenn

    As someone that has a little brother with a disability, I understand what it’s like especially in public sometimes. The things that people have said to me and my family is unbelievable but it doesn’t matter to me. I love my brother and that’s all that matters.

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  22. Christina

    Thank you so much. It is possible to share this disorder. You just did it. I am the mother of two adult children with high functioning autism. It turns out their dad has it also. So that’s three on our Aspie planet so in a way I’m the odd one out. All the best to you and your family as you travel this journey.

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  23. Kate @ Back to Basics Tuition

    Hannah, I’m sure your strength as a sibling is shared by many others around the world, your courage to talk about it is second to none.

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  24. Cordeline

    Thank you for your story Hannah and bravo to your mum for standing up for your brother and herself.

    My nephew has a son with Austim (among other development issues) and although she loves him with all her heart, the journey so far (he is 6 this year) has almost destroyed her many times. She moved her family to the other side of the world in the hope that they will get better care and aid for him because they just couldn’t afford it here in Australia.

    Everytime I talk to her it is an emotional roller coaster when she talks about her son. She often says ‘I just don’t want to do this anymore’… it breaks my heart.

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    • Anna

      Hi Cordeline, sorry to hear about your niece’s son. Hope you don’t mind me asking but just wondering where did they move to in hope of better treatment? I have a very close friend who’s 3 year old son has just been diagnosed with autism so I’m interested to know any information

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      • Cordeline

        Hi Anna

        No problems asking questions! It’s actually my sister’s son… my nephew who is Autistic :-) Sorry, I probably wasn’t very clear. I am sure there is awesome treatment/aid here in Australia, but it is just extremely expensive. They couldn’t afford private help (so to speak). So they have returned to Canada (where my BIL is from) and over there, they are eligible for a whole host of government funding for their gorgeous boy.

        x

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  25. SueBeDoo

    Fantastic article, Hannah. My good friend’s son has ASD, and while he doesn’t have the behavioural issues, he is non verbal (at 5 years old). Thankfully in her area (in the USA) they have fantastic early intervention programmes that has helped him heaps, since his diagnosis at around 2 1/2. Also, after recently speaking with my cousin in CA, she told me about some iPad apps that are actually quite good for people with autism (I would think older kids and adults) to help them communicate, including this one: http://www.imean.mobi/iMean_site/Welcome.html. (a bit of self promotion – her son, while not autistic, but has learning disabilities, actually did the programming on it).

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  26. Hannah M

    Darling Han, you’ve got such a way with words. My nephew is ‘on the spectrum’ and I often wonder what his future holds. Much love to you and your family.

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  27. vanessayoung

    What a beautiful article, Hannah. My granddaughter has autism, and I cheered when I read what your mother said to that man at the supermarket. There is so much ignorance in the community. My granddaughter has limited speech in everyday life but can read and write. She is six and will read words out of a book but cannot translate that skill into asking for a drink, for instance. When I told someone in the family that she was reading they said “yes the slow ones often are good at one thing”. I cried. Recently another family member asked if “you can use the “R” word” to describe my beautiful granddaughter. I am still grinding my teeth in anger over that one.
    Hannah, you demonstrate something I have noticed in the siblings of people with autism. You are compassionate and proud of your sibling. Thanks for adding something positive to my day.

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    • kaufman

      I can’t believe somebody would ask that! What revolting and disrespectful behaviour.

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  28. Emma

    Growing up, no one outside our family even knew what autism was . My brother is fantastic and has achieved so much and I am so proud of him, but sometimes it is difficult.. very difficult.

    I remember one school trip in year 7, when one of my class mates was flicking through Dolly magazine stumbled across an article on autism and asked stupidly “what’s autism, does that mean that your a retard or spastic or something?”

    I wanted to punch her in the face. However, I instead told her she was an ignorant uneducated twat and that one day, if she has a family and one of her children is born with a serious mental illness she might just have some understanding of how hurtful the word ‘retard’ and ‘spastic’ are.

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  29. Bronwyn

    Thank you for this article. It is beautifully written and highlights that helping people with Autism doesn’t end when they turn 5 or 7 but continues on into adulthood.

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  30. Anon

    I work with many children with ASD and I wonder what it would have been like for my father to have been diagnosed when he was a child. He is unfortunately a complete recluse and has driven everyone away with his awful behaviour; and has no ability to see his confusing disorder for what it is. It’s so truly great to see children receive early intervention and have wonderful lives. He is, unfortunately, a lost cause.

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  31. Anna

    This is beuatifully written, and speaks to the heart and point of the matter.

    One of my best friends has Aspergers and I spent most of my childhood and teenage years sticking up for her when people felt the need to ridicule her for being different.

    I have also worked as a Teacher Aide and had the priviledge of working very closely with some truly amazing students, including 2 autistic boys at different levels on the spectrum. Whilst communication was extremely difficult with them, they brought a lot of light into my world and I loved going to work.

    Thank you for sharing your study and helping shed some more light on this misunderstood condition

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  32. Anon for this

    I thought I was safe to have a quick read of Mamamia on my son’s iPad, only to discover he was in the toilet playing with his poo…one of the many sensory seeking behaviors associated with his classic autistic disorder. Meanwhile, my daughter was having a meltdown, because I bought the wrong brand of mac’n cheese…..she is high functioning, and is able to talk.

    Welcome to our world of autism. My children are amazing people. Not because of their autism, but in spite of it.

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  33. K8e.

    If only i had your wonderful expression Hannah, you could be me, talking about my brother, and our loving mother. My brother does not have autism, rather an intellectual impairment resulting from birth injury. My parents will be ‘looking after’ him, until they are too old, and then it will probably become my journey. I am so glad you wrote of the love that lives behind the misunderstandings of everyone else towards people with disabilities, such as Autism.

    Thank you.

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  34. kathl29

    Thank you for this article. I must be honest and admit I had not really thought about what happens when Autistic children become adults.

    You hear so much about it in relation to children but no one tells the stories of adults within the spectrum so thank you as your article has opened my eyes.

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  35. Belle

    Great article. All the best Hannah.

    You know, one thing I’ve never forgotten is Jenny macarthy (the anti vaccine campaigning ex-playboy model). She went on Oprah and said “my son is inside this shell and I know he’s in there and I want to get him out”. Or something to that effect, referring to the “vaccine damage” that “caused his autism”. It struck me as so terribly sad. Her son isnt stuck inside a body that has autism; her son has autism. She isn’t appreciating the strengths and differences as an individual if she can’t accept her son for what he really is. A child with autism. I thought it was a skewed (and sad) way to look at things.

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    • Michelle

      I appreciated that Jenny McCarthy wanted to bring awareness to Autism and Kudos for that. However, she is on totally the wrong track with her “vaccines caused Autism” stance. It has been scientifically proven again and again that there is no proven link between vaccines and Autism, they have been shown to be perfectly safe. The fact is that we don’t yet know what causes Autism, although there are certainly plenty of theories.
      I really hope that Jenny, like all parents of ASD kids, has learnt to appreciate her son’s positives and strengths.If she can accept him for who he is, their lives would be SO much richer.

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      • Kris2040

        Imagine if all the anti-vax people who carry on about their kids catching autism from their jabs put their energy into helping their kids and fundraising and research about ASD?

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  36. toradora

    thankyou. my husband has aspergers. and while its not severe he is very lucky in that case. but its hard. some days so freakin hard i cry for what he goes through. and sometimes because of what my daughter and i go through because of it.
    the struggle i have to get people to understand my husband is huge. alot of people seem to think autism (including aspergers) is a childhood disability something you grow out of. or as many people )including my family) put it ‘i just never thought about it.
    in my case the hurtful comments aren’t often directed at my husband alot of the time they are directed at me. people tell me i must be crazy to have married him. they ask me if i knew before hand. or why i don’t leave him. someone even accused me of child abuse for having a child with him (my child thankfully has no markers for autism or aspergers).
    I’m an integration aide. i have training in these area’s but still sometimes at 4 in the morning when I’m trying to convince him that he can go to bed and that i do really exist and i didn’t mean to call him names in my dreams (one of the completely circular arguments we have to have) i’m crying in my head why does this have to be this hard?

    just a little more awareness goes a long way. just because you can’t see a disability doesn’t mean it isn’t there.

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    • Michelle

      Your husband is a lucky man to have your love xx

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      • Michelle

        and I really hope my son will be lucky too :)

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        • toradora

          most days i’m the lucky one. i was a horrible mess with a ton of baggage of my own when we first met and he helped me through it all with a patience and understanding that was just unfathomable. these days we are strong supporting each other.
          i’ve never known a more unconditional love than his

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  37. Laurna Hamilton

    Thanks you for this, my son also has autism, and it is so difficult to live with AND to live through. There needs to be more awareness, I read that one out of ever 88 children will be diagnosed with autism. It is sad and disheartening.

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  38. Michelle

    Thank you Hannah for your beautiful and honest article. I have three gorgeous kids who are now young adults, two of them are on the ASD spectrum. I love my children with everything I have and I have given absolutely everything I have to help them achieve their potential. But it has been so damn hard and has at times nearly broken me. There have been many days when I felt like I couldn’t do this for one more minute, but of course I had no choice but to grit the teeth and keep going.
    Would I change anything about them? NO!
    Can I love them any less? NO!
    Would I choose for them to have this disability? NO!
    But having said all that, there are still so many positives to be found. I am in awe of their courage on a daily basis as they face up to and conquer their fears and achieve some amazing milestones. They have come such an unbeliavably long way, especially in the past few years and I am simply bursting with pride for these remarkable young people.
    I am so proud and lucky to be the Mum of Karina( 21, Autism), Kody(19, “normal” but an awesome sister and daughter) and Bobby(17,
    with Asperger Syndrome)
    Happy World Autism Awareness Day!!

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  39. Ljs

    Beautiful writing thankful Hannah.
    I was thinking that as autism awareness increases there does seem to be an increasing idea that people are just getting autism diagnosis to get govt funding – even some friends who have seen how horribly difficult it has been for my family say this!
    I would happily return all the funding to see my son develop friendships with his school peers rather than having no concept of friendship.
    Best wishes to your family & to all the families affected by ASD.

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  40. KJJ

    Thank-you Hannah for your brave and honest story.
    I also have a son with Autism and a daughter, his much loved sister.

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  41. kirstys

    Hannah, your parents are living my future, you are living my daughter’s future. It’s hard for me to comprehend and I’m already on that journey to awareness of what my life will be like – forever – because “the luck of the draw” means my son has autism and a global development delay. It’s not the rosy future I envisioned, but it will be a little easier for me because of families like yours that have gone before me. Thank you for speaking up.

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