What happens when you finally get the diagnosis that explains your entire life… but it doesn’t bring the relief you expected?
In this episode, I share my personal story of receiving an autism diagnosis at age 36. We talk about the emotional weight of late-diagnosis — the grief, the exhaustion, the clarity, and the quiet rage of realizing just how much could have been different with earlier support.
I break down what the diagnostic process was actually like, the lack of resources available to late-diagnosed adults, and how it feels to confront decades of misunderstanding — from others, and from ourselves.
We also dive into something urgent happening right now: U.S. Health Secretary RFK Jr.'s plan to create a national autism registry — without our consent. We unpack the dangerous implications of this kind of surveillance, especially in a post-Roe v. Wade world where HIPAA protections have eroded, and we explore what it means to advocate for disability justice in a time when our autonomy is under attack.
This episode is for anyone who’s ever felt unseen, unsupported, or like the world wasn’t built for their brain. You are not alone. Your story matters. And your voice is powerful.
This is about more than labels. It’s about who gets to be seen, supported, and safe in the world.
🧠 You are not too much. You are not alone. You are not broken.
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