Quotes About Autism (and everything that includes)

  • Prof Michael Fitzgerald, Henry Marsh Professor of Child and Adolescent Psychiatry at Trinity College Dublin, and the author of The Genesis of Artistic Creativity: Asperger’s Syndrome and the Arts, speaks about people with Asperger’s Syndrome. In his book, he has this to say about Asperger artists:

Persons with the syndrome are often workaholics, highly persistent, content with their own company and solitary artistic occupations; they focus on detail with massive curiosity and total immersion; they are novelty-seekers in terms of their art, with massive imagination in their specialised spheres. They are also far less influenced by previous or contemporary artists in their work than are ‘neurotypicals’. It appears that the autistic artist, because of his or her rather diffuse identity and diffuse psychological boundaries, has the capacity to do what the artist George Bruce described as being necessary for art: ‘One must not just depict the objects, one must penetrate them, and one must oneself become the object’.”

  • Morton Gernsbacher, parent of an autistic child, says:

” … research demonstrates that autistic traits are distributed into the non-autistic population; some people have more of them, some have fewer. History suggests that many individuals whom we would today diagnose as autistic – some severely so – contributed profoundly to our art, our math, our science, and our literature. “

Autism itself is not the enemy… the barriers to development that are included with autism are the enemy. The retardation that springs from a lack of development is the enemy. The sensory problems that are often themselves the barriers are the enemy. These things are not part of who the child is… they are barriers to who the child is meant to be, according to the developmental blueprint. Work with the child’s strengths to overcome the weaknesses, and work within the autism, not against it, to overcome the developmental barriers. You do not have to wipe all of us out (“cure autism”) to solve the problems that the low-functioning autistics face. As I see it, autistics are another kind of person, almost like another species, that has an unfortunately high rate of sensory dysfunction and resultant mental retardation in its children. You do not have to get rid of the whole group (again, by that, I mean curing autism) to get rid of the retardation that is all too common among my kind. That would be like trying to get rid of sickle-cell anemia by “curing” blackness (eliminating blacks). We have too much to offer society for that to be allowed to happen… if we are helped to develop as much as possible. I think that is a great and wonderful goal, and I hope you will agree.”

  • Larry Arnold has this to say in regards to his own autism:

“I didn’t get where I am today by not being autistic.”

  • Trisha Van Berkel says:

“Autism is not a puzzle, nor a disease. Autism is a challange [sic], but certainly not a devistating [sic] one.

Autism is about having a pure heart and being very sensitive… It is about finding a way to survive in an overwhelming, confusing world… It is about developing differently, in a different pace and with different leaps.

Autistic beings develop and bloom if their spirits, talents and self-esteem are not destroyed by bullies, prejudice, ‘doggie-training’, and being forced to be ‘normal’.”

This is what we know, when you tell us of your fondest hopes and dreams for us: that your greatest wish is that one day we will cease to be, and strangers you can love will move in behind our faces.

  • BTW, this one by Jim Sinclair reminds me of the line from the movie Batman Begins, where Ducard says this to Bruce Wayne:

But I know the rage that drives you. That impossible anger strangling the grief, until the memory of your loved one is just… poison in your veins. And one day, you catch yourself wishing the person you loved had never existed so you’d be spared your pain.

Autism (with a capital “A”) to me, says that I accept my child wholly. I celebrate his differences and his quirky-ness. I advocate diversity. I try to empower him. I am proud of his successes, no matter how small they seem. I hope he holds onto the compassion he has in his heart into adulthood. I do not think he needs “fixing”. I am proud that he is my son, and sometimes I am humbled by that very same thought.

  • Parrish S. Knight has this to say:

Autism is not something I have. It is integral to who I am. Eliminate the autism, and you eliminate me. When you say you want a cure, you are saying I should be put to death. Think about it.

  • According to my (lastcrazyhorn’s) main music therapy professor:

Empathy is not defined as feeling the same as another (as she pointed out, that’s codependency), but rather the ability to hear what another is saying and to tell them that you heard.

Retrospective consideration of the lives of exceptional human beings offers credible evidence that the autistic distinction has persisted throughout history, and has been a valuable element of human culture. Genetic research indicates that at least twenty different genes can signal a predisposition to autistic development; autism is pervasively embedded in the deep structure of humanity. Psychological research indicates that autistic characteristics constitute an identifiable pattern of traits that are present in varying degrees throughout our entire species.

Autism is as much a part of humanity as is the capacity to dream.

  • Awalkabout has this to say about autism (and her children):

Autism means your children approach our world differently. We just need to learn to interface through therapy, play, school, medical interventions, depending on the child’s needs. Give them the tools they need so they can communicate and understand; but I’m not one of those who insist on a cure. Our children have various gifts and instincts that might well be changed if they no longer had autism—I don’t want to lose those.

Don’t underestimate persons with autism, try to understand.

Asperger’s syndrome has probably been an important and valuable characteristic of our species throughout evolution.

Someone with Asperger’s really is like you, just more extreme.

  • “Lines in the Sand” – from House M.D.:

Cameron: Is it so wrong for them to want to have a normal child? It’s normal to want to be normal.

House: Spoken like a true circle queen. See, skinny socially privileged white people get to draw this neat little circle, and everyone inside the circle is normal, anyone outside the circle should be beaten, broken and reset so they can be brought into the circle. Failing that, they should be institutionalized or worse, pitied.

“Appropriate treatment” is not possible unless and until educators adopt a policy of unfailing respect for the individual. Progress is more important than a cure. Acceptance of difference is more important than achieving normalcy. Tolerance is not good enough because it demands change or at least movement toward an external norm.

I deserve acceptance and respect as I am.


15 Responses to “Quotes About Autism (and everything that includes)”

  1. [...] way, I’d like to think that the quotes on my quote page include both information about AS and hope; effectively combining the [...]

  2. Frank Klein has it all wrong. Autism and retardation do not belong in the same sentence. I am offended by him implication and I fear he is autistic and has bought into the drival of “normal” people. On the other hand, Trisha Van Berke, hit it dead on. Society had done more to harm the autistic then help him/her by trying to force “normalcy” on them. WHO is it that knows the absolute truths in this universe to be qualified to defined normal ? No one. Perhaps autism is the evolvution the human race so that we may have a future. Who is to say it is not?

  3. [...] I have that quote listed on my autism quotes page. [...]

  4. Do we or do we not want to see THE CONDITION of autism cured, healed, alleviated, and not just treated? Why is there so much debate about this topic? Either autism is desired or undesired. Period.

    I have not seen this type of contest on blogs related to cancer, juvenile diabetes, arthritis, and other diseases. It seems the folks talking about cancer agree that cancer is not desired. Hum, what gives when we discuss autism? I am truly perplexed by those who are vehemently opposed to a “cure.” Are you suggesting that the inability to speak, self-injurious tantrums, sensory issues, little to no social interaction, unexplained wetting, and other autism manifestations should be customary for any family? If that’s the case, then let a round of autism be distributed to each and every family across the globe, and perhaps you’d be interested in a double portion. That would settle it. No further debate needed. Autism would be “normal” and desired.

    I want to understand how you all see this. I watch my family deal day in and out deal with the impacts of a home with low-functioning autism. Given what I see every day, I was disturbed to see someone here suggest that autism is an evolved state. Wow…

    Okay, no more middle ground. Is autism desired or undesired?! Period.

  5. Boy, and they say that aspies only see things in black and white . . .

    More later – I’m about to run off to a symposium on natural healing.

  6. i really think the IDIOT who is asking whether or not Autism is desired is ridiculous! You have lotsof nerve to imply that parents of children with Autism are the ones that dont want a cure.
    It’s the AAP and the vaccine companies that will not admitt and take repsonsibilty for their actions. When they do…we have preventiona and all the facts we need to move forward with finding a cure. So don’t sit there and impky that us parents don’t want a cure!

  7. I am not a parent with Autism, but my great-nephew has it and I watch my nephew and his wife do an amazing job of working with him. He has, as I have witnessed with my own eyes, become part of our world again and is trying hard to come completely in. I think the person talking about “desiring autism” was actually responding to someone (I thought it was someone with Autsim) saying that we should not find a cure but work within the boundaries of autism. ANd I believe he/she disagreed. The way I am reading your posts, you are both on the same side. No one who has seen low, moderate, or high functioning autism wants to see their loved one go through an ostrisized life. No one of any worth considers them just a “science project”. And no one, not even the parents of children with Autism, considers their child “second class” or “not as good as the others”… We must not get off on some tangent and not see the whole picture. May God give us the key to unlocking this door for all our sakes.

  8. By the way, in addition to what I said above, I have NEVER seen a gift taken away as a child becomes more able to communicate and realte without anxiety to his/her world. Autism is not the gift “the gift is the gift.” That will never be taken away. I have a brother with Aspergers. He has incredible talents in many areas. As he has learned to become more social, to interact more ably and to learn to care about others more, his gifts have NOT deminished.

  9. @ Perplexed. You really should learn what is autism before even judging what others are saying about this.
    Whether or not it is desired is not even a discussion amongst us who do have it, as there is no cure senseless talking about it is of no use and serves no one.
    But do remember that even if autism is a pain to us, I also from my heart can say it has been a beautiful gift. But talk WITH us not about us. So if you need info mail me @ erwin@herow-international.com
    Ohh and before you say something I am diagnosed Asperger Syndrome, wrote several articles in a Dutch Newspaper about it (www.nd.nl) and spoken about at 2 conferences about this (see http://www.kijkzieontdek.nl) So don’t think I do not know what I am talking aboutm before you start yelling.

  10. Can you provide better citations on these quotes? I would like to know them for my research paper.

  11. Hmm.. is inspiring as we have an asperger kid & just like most comments we truly believe our kid is genius in one way or others… And tks for these quotes that I can always use to encourage my wife & me.
    You can see our son when he is 4 yrs old.

  12. My concern with the “cure” is severalfold. My son has autism. We have been working through multiple systems struggles since Jimmy was 16 months old. Despite multiple obstacles, Jimmy is a gift. His level of innocence, compassion, and depth of character are displayed in multiplicity.

    If a cure was presented, what would the potential side effects be? This would engage more research, potential side effects, and unknown long-term effects. For parents who have negated diagnosis, treatment, or interventions while waiting for the “experts to find the cure,” multiple opportunities have been missed, because medical researchers continue to present a new cause every 6 months, and every celebrity with a child with autism is presenting a cure every 3. One size does not fit all in children with autism.

    Having researched this phenomenon, written a dissertation, and speaking regularly at conferences on this topic, I can honestly say that what is needed in this situation is a higher level of long-term understanding societal impacts as opposed to some kind of “quick fix” that will only be presented years from now and may only impact a few, such as those willing to take the risk of what a potential cure might imply.

    If anyone suspects their child might be autistic, please seek intervention immediately.

  13. I stumbled across this site by google. I like it. Growing up my parents always just told me I marched to the tune of my own drummer. I went with it. My parents never questioned me when I started to sleep on the floor and contined to do it for 5 years. They never questioned my insane desire to organize their National Geographics by month and year and have them complied neat and orderly. I was me and that was just peachy.

    It never really dawned on me that my closest friends are people that I’ve known since I was a child. I really hate making friends. I never realized it was weird to eat insane amounts of hot sauce… that is just me. I didn’t realize it wasn’t normal to laugh when something went wrong. I didn’t realize it wasn’t normal to prefer to sit on the floor versus a desk when you have an office job.

    I didn’t realize this until I obtained a job that involved me to work with other adults. The funny thing about it was I’ve been working in social work since I graduated college. The wonderful people that I have gotten to work with have pointed out that I’m not normal. My newest peer that I have started to work with thinks I have ADHD and am some where on the autism spectrum. Her husband is ADHD and she told me we are two peas in a pod. I have to smile when she says this. Sometimes it is more fun to be different.

    Point being if my parents hadn’t accepted me for who I was…I’d be a lot different. They embraced my most eccentric behavior and often times just laughed. If my parents wouldn’t of been as supportive of me as they were…. I probably would of thought that I wasn’t normal. Now I’m very okay with it and just continue to march to the beat of my own drum.

  14. I am a mum of two little boys with Autism. My life is not what I imagined it would be in having children…. but would I change it… no. I love my boys for who they are. Autism doesn’t define who they are, but it is a part of them. Sure there are days that feel unbearable and beyond challenging but there are also many, many days when I look at my boys and realise that they are the best teachers I have ever had in my life.

    I look at how they approach things, how determined they can be when they really want something, I marvel at how they don’t care about what anyone else thinks about what they are doing or how they are behaving, especially when they are having fun. I marvel at their sense and sensitivity for people and places. I marvel at their talents,I am humbled by their struggles and I appreciate and celebrate every single little milestone they make.

    I love their character, their individuality, their quirky-ness and I will never put a limitation on what they can and can’t do. I will encourage them to dream big and I will do everything in my power to try and help them make their dreams come true.

    Great blog by the way :0)

  15. @princessbride: I understand what you’re saying, and if my children had “gifts” like some people have “gifts,” I would believe that, too, that they would maintain their abilities no matter what else happened. I think my daughter’s advantage is that she sees through to the heart of things because she is literal, because of the autism. My son, on the other hand, as much as I wish he would have one of those narrow interests so that we could inspire him to follow it, he doesn’t. He just has behavior that continues to disrupt everything. He says he doesn’t know why he can’t control himself. He has no governor between “think” and “act.” We’re all still learning how to deal with it.

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