Looking for Normal

How an autistic boy became a successful musician, husband and father.

Looking For Normal is the memoir of author, musician and filmmaker Steve Slavin. His obsession with music led to a long career in the creative arts – albeit one defined by depression, obsessive-compulsive disorder and cognitive impairment.

Steve recounts the forty-eight years that led to his autism diagnosis in 2008. This darkly humorous memoir will inform and inspire anyone with an interest in autism and mental health. But more than this, Looking For Normal is the story of ambition and courage set against a backdrop of low expectation and the long shadow of traumatic childhood dysfunction.

Reviews

“Insightful, inspiring, informative and entertaining. Looking For Normal is not just about overcoming the adversities that life throws at you on a regular basis. It is also about someone’s journey of accepting, embracing and celebrating everything that comes with having autism.”

Dr Rai – Senior Practitioner, Educational Psychologist.

Looking for Normal - Introduction

If someone had told me that one day I would write a book about autism and mental illness, I would have looked over my shoulder to see if they were talking to the person standing behind me. Yet, here I am, having written almost three hundred pages of gut-wrenching self-analysis; exploring in depth those very things: autism and mental illness.

Looking for Normal was not, however, the first title that came to mind. I almost went with Autism—And All The Other Complicated Stuff I Was Too Embarrassed to Talk About, But Did Anyway. I rejected this idea, not because it would have been an inaccurate description of the book’s content, but because it would have been far too long to fit neatly on the cover.

Can I Start Again Please? Was another title contender: if only I could restart the clock at 1959 and have another go—but this time as a knowingly autistic person.

Eventually, after weeks of insomnia-inducing procrastination, I decided that Looking for Normal best describes my valiant, if often farcical attempts at life: a life darkened by the long shadow of my assumed childhood abnormality. Ah, yes—my childhood. I mean… what the hell happened back then? Why had the doctors described me in ways that would have today’s politically correct brigade foaming at the mouth? The doctors said I was abnormal, maladjusted and emotionally disturbed. Surely it was not ‘normal’ to spend the majority of one’s childhood being psychologically prodded and poked, medicated and hospitalised.

Someone who knew me as a child recently remarked that after such a wholly dysfunctional start in life, it’s a miracle I’m still alive, let alone been able to raise a couple of kids, stay married for thirty years and achieve a modicum of success in the music business. I’m not sure whether I should feel flattered or saddened by their comments: because being a person for whom the glass is generally half-empty, I can only reflect on the things I haven’t achieved in life; how things could have—should have been.

Aside from the tricky task of choosing a title that sums up the entirety of one’s life in a snappy three-word strapline, there are a number of other things to consider when writing a memoir, or autobiography as some may choose to call this book. For example, how deeply can a writer navel-gaze before their poetic ramblings become little more than unattractive narcissism? And just when, exactly, does healthy introspection sour into tedious self-indulgence? These are judgements I shall leave for others to make. Because, having spent five years crafting sentences from emotions pulled kicking and screaming into the light, my sense of literary balance is well and truly dulled.

Writing a book such as this is difficult, and I have battled endlessly over the amount of personal detail that needs to be shared. I would describe this process as being similar to instigating an extraordinarily embarrassing conversation about things you’d rather not discuss, with strangers who may not be in the slightest bit interested in anything you have to say.

I’ve heard it said that you never finish writing a book. You just decide, at some point, that it’s time to put the pen down. I have reached that place, and I am as happy as I’ll ever be that I have told my truth in the best way I can. It’s time now to submit my tale of life, love, autism, and all the other complicated stuff I really didn’t want to talk about—but have, anyway.

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11 responses

  1. I’m a woman with late ASD diagnosis too, and I very much enjoyed your interview with Anna C. Wilson about her book ‘A Place for Everything’. I came across it after hearing Woman’s Hour saying they would be talking to Anna Wilson the next day. Your interview was a revelation, in depth and insightful, which can’t be said for the Women’s Hour interview. I recognized so many behaviours from my own mother, as well as from myself. I feel very resentful over a lifetime (in my own case) of presenting to the medical/clinical profession in distress, often with anxiety and depression, and never, until I was 50, having ASD mentioned by anyone (and even then it was down to my new G.P. having ASD in her own family). It was also only after this that I learned about the connection between digestive / gastric problems and ASD (which Anna mentions her mother had). The lack of connection between, as you say, medical services – even mental health services – and knowledge and experience of autism is astounding, and there is so much hidden torment and suffering due to this I have thought and read and written a lot about the different ways females present with ASD than males – whole articles. Some of this is on Academia.com, and some on the now defunct Verbal Remedy site. After my diagnosis I wrote a novella about a woman getting an ASD diagnosis, and the effects (inc. suicidal impulses) of all the confusion and contradiction this brings to her, and ‘published’ it on Amazon (title: ‘Ta-ra, Alice’), but less than a dozen e-copies have been downloaded. I don’t, and wouldn’t know how, to make people aware of it. Thanks for your work (I can’t buy your memoir at the moment as it’s not available, but would like to in the future).

    1. Hi L Bonneville.
      Thank you for watching my interview with Anna. Her book will help a lot of people understand their own adult autism.
      I can definitely relate to the thing you said about feeling resentful and struggling through to 50 years of age without a diagnosis. Almost identical to my situation. It’s important that we get our stories out there to educate medical professionals, and also other mature people who feel they may have autism.
      I will have a look at your book on Amazon. And I will let you know when mine is re-published.

      Many thanks
      Steve

  2. Hai again, Steve. Thanx for letting me know your book is back in stock at Amazon—I just purchased both a paperback and kindle edition. Btw, I have you beat: I received an ASD diagnosis at age 56—not so much a “very late diagnosis” as it is a TOO late diagnosis. 😉

    1. Hi Mustafa
      Thank you for purchasing my book. I really appreciate this. Yes, you definitely beat me in age to a diagnosis! I don’t think 56 is too late though. I’ve just hit 60, and life is just beginning!
      Best wishes
      Steve

  3. Hai. I read an article in Spectrum which mentioned your recently published book, soI did a search on Amazon but it is listed as not available. Just wondering if that status will change. Thanx.

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