Welcome back to another Founding Member Friday!
Every other Friday, a post like this will be brought to you by and for our Founding members.
The first part of this post is FREE to everyone here on Substack, and the ending of the post is ONLY available to our Founding Members (as thanks for the extra support they give to make this blog possible).
We currently have eleven founding members. I won’t put them on the spot today, but you know who you are. I can’t thank you enough for your support.
The NeuroDivergent Rebel Blog is a reader-supported publication. I hope you’ll join me as a free member (but I also have paid subscriptions if you want access to bonus content).
Also, per request from some of you who weren’t her in March when I did the initial sale: for a limited time the 50% off sale is back (details below).
Currently, for PRIDE MONTH paid annual subscriptions are 50% off (only $25) your first year when you subscribe now through the end of the month.
Since my Autism diagnosis almost seven years ago, there is one question I’ve been asked with reasonable consistency.
This week on Founding Member Friday, I answer one of my most asked questions:
Do I wish I could have been diagnosed Autistic sooner?
CONTENT WARNING: This article contains discussions of Autistic Conversion Therapy, also known as ABA (Applied Behavioral Analysis)
When I was first diagnosed, my answer would have been a solid “Yes!” because of all the confusion and pain from not knowing I was Autistic for the first 29 years of my life, but today (knowing what I know now), my answer is a solid “nope” (for multiple reasons).

Finding out I was Autistic after a lifetime of being hard on myself (and everyone around me) left me drowning in a multitude of emotions, including all of the five stages of grief (denial, anger, bargaining, depression, and acceptance).
Learning I was Autistic as an adult doesn’t mean I was “suddenly Autistic” after years of not knowing.
I am (and always have been) Autistic, meaning my life (and all the moments in it) have been influenced by my Autistic mind even when I didn’t know the truth about my brain.
Growing up thinking you’re something you’re not is a traumatic experience.
I was taught (because nobody knew I was Autistic) to emulate and “be like” non-autistic people – an unfair goal for someone with a brain like mine. The non-autistics around me were the ones who set the pace, the expectations, and the bar for success – a bar that was (for me) almost always out of reach.
When I failed to measure up (when compared to the non-autistics around me) I was often scolded, mocked, and punished, or “encouraged” to “try harder” and apply myself “more” (even though I was already doing my best and trying harder than most people around me).
I have a core wound, that I am not enough. This wound extends into everything I do.
Even when I do something uniquely wonderful, I struggle to see my gifts and talents as such (because the critiques I’ve heard my whole life have become engraved in my mind “try harder,” “a little bit more,” “do better,” “are you going to quit now?” pushing me past where a reasonable person would have stopped).
Even though I was not labeled Autistic for most of my life, I (a visibly NeuroDivergent child) did not escape the stigma of the Autism and ADHD BrainTypes I carry.
My struggles were visible, especially in school, where my cries for help and unmet needs were labeled as behavioral issues (that needed to be extinguished so I could be less inconvenient to my teachers and peers).
I didn’t know I was Autistic, ADHD, or Hyperlexic back then (nobody knew), and because nobody knew the appropriate labels to call me, others were applied:
I was bad – when asked too many questions, or I couldn’t sit quietly in my seat, giving the teacher “appropriate attention” (staying seated, not making vocal sounds, with my eyes on her, my feet on the floor, and my hands not moving).
I wanted to be good – but my body and mouth had a mind of its own. Even now, my body will often move without my realization or direction, but as a kid, my body (and mouth) was much more challenging to control.
I was stubborn, difficult, and rebellious – when I froze up from anxiety or didn’t have enough information (or confidence) to start something.
I wanted to act but was stuck frozen – and the punishment and scolding didn’t help ease my anxiety or motivate me.
I was sensitive, moody, and dramatic – when I felt exhausted and overloaded by overwhelming sensory environments or big feelings.
I wanted to “keep it together” – but I couldn’t hold in the emotions and pain any longer.
I was manipulative, pushy, and inconsiderate – when I tried to be firm in my needs, struggled to articulate my needs verbally, or had meltdowns because of not having my needs validated or accepted.
Eventually, after years and years of being called all these names (and many more that are MUCH worse), I began to believe all the negative things people said about me.
Because finding out I was Autistic was the magic word that took all those other words away when I first learned this fact about myself. At that time, my primary emotions (after the initial phase of trying to disprove my diagnosis by reading other Autistic People’s stories and only managing to convince myself further that I was, in fact, Autistic) were anger and frustration at the years of not knowing.
Back then, not knowing what I know now, I would have given anything to have known I was Autistic earlier in my life.