About the Author

I am a 50+-year-old American woman of predominantly Western European (in particular mid-European, Cornish, and Eurasian) descent. Throw in a little West Africa (via the Caribbean slave trade), Papua New Guinea, indigenous South America, indigenous Taiwan, and globally distributed Jewish roots, and you’ve got me.

I consider myself a full-blown Aspie. As of this writing, I have not been formally diagnosed. I have not been able to verbally communicate effectively with anyone qualified to deliver that diagnosis. I have been assessed by a qualified professional and yes, I’m Actually Autistic. I have been searching for some time for a professional who can assist me, as well as the financial means with which to pay for a qualified assessment. But because of the following issues, I was unable to get a competent diagnosis:

  • social anxiety
  • visual, non-verbal cognitive and communication process
  • alternative comprehension of spoken vocabulary
  • impaired social facility with professionals
  • all-’round asocial Aspergian tendencies

Fortunately, as of September, 2016, that irritation is behind me. I have corroboration from a professional, so let’s tick off that box, shall we 🙂

As a child, I was intensely withdrawn… was unable to form lasting relationships with peers… I refused to play with toys as they were (I took apart the vacuum cleaner my parents gave me and played with the parts individually, and I dismembered and reassembled the dolls with which I was supposed to simulate/practice parenting)… I was fascinated — often to the exclusion of all else — with spinning objects… I could not fall asleep unless I rubbed the satin edge of my blanket till it was threadbare… I read books written for individuals well beyond my assumed developmental level, yet I comprehended almost nothing of what I read… I self-injured in times of intense personal distress… I talked to myself constantly… I was highly sensitive to touch (so that sometimes even the most loving touch felt like a blow, and when people hugged me I felt like they were beating me)… I lashed out against my siblings and melted down frequently, and my anti-social behavior and feral manners humiliated my parents, who were leaders in their community.

When I was growing up, there was very little understanding of autism or its various spectral manifestations, and my parents did not have the means to pay for special care for me. I was in and out of special programs in school, as well as therapies. Nothing seemed to help my continued distress, or improve my “bad” behavior. The best anyone could hope for me, was that I would stay out of jail and find a regular job, someday. I don’t think my parents ever expected me to turn out as independent as I did.

In spite of negligent treatment by people who either assumed there was nothing wrong with me or I would eventually grow out of my troubles, I have managed to piece together a life of considerable accomplishment, while keeping my deficits well out of public view. My Aspie traits have persisted, including those you’ve read about in the prior pages. I have been covering for my lack of functional abilities my entire life, and I have done everything in my power to hide them from a judgmental, prejudiced, and predatory world — including friends and family.

Since I was a young girl, I have wanted to be a writer. The best writer I could be. I have made a career (albeit unpaid) of observing and studying the human race in exquisite detail. For most of my life, I told myself it was so that I could create believable fictional characters. Now I realize that the fictional character I’ve been creating all these years, is myself.

Like Liane Holliday Willey, I am adept at “pretending to be normal.” I am the Aspie among you who has gone undetected throughout my adult life, because I removed myself as far as possible from all the people who knew me as a troubled child and teenager.

I own a house, have a successful technology career, and since 2004, I’ve been legally married to my same-sex life partner of 25 years. I am also a part-time executive with a non-profit volunteer organization. Life goes on, regardless of all the ups and downs. Yep, life goes on.


Did you enjoy this? Please consider becoming a patron at Patreon.

19 thoughts on “About the Author

  1. I’ve enjoyed discovering your writing and sharing – I hope life is going well for you. Strangely I remember my own almost pathological reliance on the soft smoothness of the satin edge of a blanket in order to comfort myself as a child. My mother purchased three to ensure we were never without one.

    Liked by 1 person

    1. VisualVox

      Thanks very much! Wasn’t satin the best? I think my mom thought I’d stop rubbing, when I wore through it. I just moved to a different part of it, and I turned the edge of the blanket into a tattered mess. I don’t think anybody realized just how important it was to me. Oh, well. Now I can provide for myself 🙂

      Liked by 1 person

  2. Liberty of Thinking

    “As a child, I was intensely withdrawn… was unable to form lasting relationships with peers… I refused to play with toys as they were (I took apart the vacuum cleaner my parents gave me and played with the parts individually, and I dismembered and reassembled the dolls with which I was supposed to simulate/practice parenting)… I was fascinated — often to the exclusion of all else — with spinning objects… I could not fall asleep unless I rubbed the satin edge of my blanket till it was threadbare… I read books written for individuals well beyond my assumed developmental level, yet I comprehended almost nothing of what I read…”

    Absolutely amazing, like you’ve read my unwritten autobiography 🙂
    Except for I have eaten half of my blanket, fluff by fluff, because these fluffs refused to be arranged in an order less disturbing for my brain/mind…
    As for my toys, they were a big box of wooden shapes, assembled every day in the same shape of a gate with a triangle at the top, and everything else around that, but same every time…
    Yep, and read Darwin in elementary school, also Maupassant, Balzac etc, before the age of 10…
    And dismantled every toy I’ve got, and they were nearly all made of tin… Spinning cogs were my real toy…

    Thank you, will be following.

    Liked by 1 person

  3. Catana

    Thanks for following my blog, though I wish there was some way my aspie blog would come up when I comment on aspie blogs, instead of my writing blog. Coincidently, I bookmarked your blog this morning after one of your comments, because it looked interesting. Once I have a chance to read a bunch of your posts, I’ll probably follow you.

    Liked by 1 person

  4. Catana

    The problem is that I also reply on writing blogs, so it would mean constantly switching back and forth. But that might be what I have to do if I’m going to grow Disorderly Minds.

    Liked by 1 person

    1. VisualVox

      I have that same issue. I wish there were a better way to accommodate our variety of personas. Oh, well. I guess it means use a different browser for each one. That’s what I do – Vivaldi is one persona, Chrome is another, Firefox is another, Opera is another. I draw the line at IE, tho’. Just can’t bear to use it.

      Like

  5. Catana

    Hmmm. That might be a good idea. I use Firefox, and once in a long while, Safari, which is painfully slow. But I’ve read about a very basic, very fast browser that might do the trick.

    Liked by 1 person

  6. I too have been a closet Aspie so it is nice to see that there are others like me out there. When we were children in the 50s, 60, and 70s autism was not as recognized as it is today. It was rare to get that diagnosis especially since you are a woman. I am glad that you finally got the confirmation you needed.

    We share many of the same characteristics. But, since I have also been deaf for the last 30+ years that has cut my social life even more. It is nice to see you are coping well. We all gotta live the life given us to the best of our ability, don’t we?

    Looking forward to reading your past and future posts to get to know you more. You are now on my daily Feedly list.

    Liked by 1 person

    1. VisualVox

      Thank you very much for writing. Yes, times have certainly changed, and we have a lot in common. Interestingly, I’ve been realizing, lately, how my hearing difficulties have really impacted my social life. I don’t hear sounds properly, most of the time, and I have to listen really carefully to understand what others are saying. If I’m not paying attention, it’s all a muffled “mffgrblllnfff”. I never thought it affected me as much as it has, but to be honest, if I don’t have a lot of energy, I can’t be bothered to listen. So, I’ve missed a whole lot in my life. I just don’t qualify as deaf.

      Anyway, it’s all part of the great stewpot of life. Keeps us on our toes, that’s for sure!

      Thanks again for writing, and I hope you get something out of my posts!

      Like

  7. I am also a 50 plus Aspie woman, self diagnosed but confirmed by a psychologist to fit the DSM V criteria. Opted not to get a formal evaluation because I have already developed coping mechanisms over the years, as challenging as it has been. I can relate to a lot from your blog, the only difference is I grew up in India. That wasn’t even a concept when I grew up. Nowadays there is so much more awareness and guidance. I happened to join one group from India and one of the moms prompted me to share my journey as a way to help their understanding with their girls. So I did start my own blog a couple of weeks ago. I have not shared my diagnosis with friends and family much so keeping it anonymous. My goal is to help others on the spectrum too. How do I get my blog out there? Any advice? My blog website is http://www.aspieblossom.com
    Thanks.

    Liked by 1 person

What do you think? Share your feedback - and feel free to share this post!

This site uses Akismet to reduce spam. Learn how your comment data is processed.