The Places That Never Knew Love

What I didn't know I was grieving, and what I've found on the other side of it

· ADHD,Parenting with ADHD,Grief,Identity and neurodivergence,Family systems

The fridge in my office has needed cleaning out for a week.

I know this because I keep opening it, staring at it, and closing it again.

I'm supposed to be writing.

I open six tabs instead.

Close them.

Open them again.

This is what ADHD paralysis looks like from the inside — not laziness, not avoidance, just a brain that needs one small, finishable thing before it can trust itself with a big one. So I clean the fridge. Start to finish, five minutes, done. The little hit of completed is enough to get me back to the page.

If you know, you know.

Welcome to my brain

Herding cats. If You Give a Mouse a Cookie. Nothing here is a straight line — there's a whole chain of mental gymnastics that has to happen before I lock into "go mode." ADHD doesn't touch one part of my life. It touches all of it. I'm sharing pieces of mine not because they're universal, but because I hope you'll feel less alone in yours.

My ADHD, anxiety, and depression diagnoses are still new. My neurodivergence is not — it's been there since I was small, just wearing other people's words for it.

Street smart. Artistic. A great reader of people. A daydreamer. Scatterbrained. A performer. Introverted.

That's what my family called it.

What I'm learning now is that a lot of what got called personality was actually an undiagnosed, genetic, neurodevelopmental difference. Nobody was wrong about who I was. They just didn't have the word for why.

The gate that never knew love

I've been sitting with something from the grief work of Francis Weller, who names several distinct kinds of grief we carry — one of them being for the parts of us that never got to be met, seen, or loved for what they actually were.

That gate has my name on it.

Because here's the thing nobody tells you about an adult ADHD diagnosis: it isn't just relief. It's also loss.

It's grief for the little girl who was, by every account, big. Big personality. Big imagination. The kind of kid who could've written songs for Sesame Street and meant it — that's not me overselling myself, that's just accurate. And somewhere along the way, that bigness became a liability. Too much. Too loud. Too scattered. Missing cues she didn't know she was missing. Struggling to advocate for a need she couldn't yet name.

So she made herself smaller. Quieter. More manageable.

And the parts of her that stayed big — the ones that never learned they were allowed to — those are the places that never knew love. Not because no one loved her. Because no one knew what they were loving, or what it needed.

I built a voice instead, one that told me I'd never get it right, never be enough, never quite belong. I carried that voice for nine years of motherhood — through three kids, before I gave myself the gift of psychological testing to official receive what I was certain of for years. Nine years of quietly believing I was the problem, and just couldn't get this mom stuff right, instead of understanding I had an unmet need.

I'm not going to pretend that's been easy to unlearn. It hasn't. And I'm still unlearning.

But grief that gets named can move. And this grief has been moving — into something softer, something closer to tenderness, for every version of me who was doing her absolute best with a brain nobody had explained to her yet.

What was actually happening

Before treatment, I lived in more or less constant sensory overload. When I couldn't access the executive-functioning part of my brain, I'd either check out completely or come out swinging at whoever was closest. And underneath both, a quieter voice kept asking, You're a good listener — why can't you focus on what people are saying? You're not a yeller — why are you yelling?

I wasn't broken. I was overloaded, and I didn't have the map yet.

Planning and memory are still hard for me — short-term, long-term, all of it. What moves me is a deadline, a challenge, or the fear of letting someone down. Tell me you're stopping by in ninety minutes and my house, which has looked like a disaster for a week, will sparkle by the time you knock. (Please don't open the closets.) That's the hyperfixation talking. The same brain that will scrub an entire house in ninety minutes will also let six cups collect on my nightstand and lose an entire hamper of laundry to time.

Consistency is the ADHD brain's hardest ask. One of the biggest shifts in my life has been giving myself permission to actually be inconsistent — to stop treating it as a character flaw and start treating it as a known feature I can plan around. That takes grace. A lot of it. Enough to let go of the shame long enough to take one small next step.

From my own repair to our repair

This is where it stopped being just my story and started being a family one.

Therapy and medication didn't just help me as an individual — they changed how I show up as a partner and a parent. I can see now where I want more consistency, and how to actually build it with my kids instead of just wishing for it. Something as small as everyone clearing their own plate, or a ten-minute tidy before bed, is possible now. Those small, boring moments feel enormous. They feel like connection.

I've also learned to say the quiet part out loud to my husband, Mike — I'm in go mode right now, (hyperixation) can we work with it or pause it — instead of leaving him to guess which version of me walked in the door.

What I'm still learning, over and over, is that when I don't tend to my ADHD, my anxiety and depression get loud, and that volume lands on the people I love most. Like most of parenting, if I don't care for myself first, I run out of care to give anyone else.

What I'd want you to take from this

If any of this landed for you: find your people. A primary care provider, a psychiatrist, a therapist, psychological testing, a friend who won't flinch when you tell them the truth. Build a team that's rooting for you, not just managing you.

And grieve what needs grieving. The years you didn't have the words. The version of you who made herself small so she'd be easier to love. She didn't need to shrink. She needed someone to meet her as she was.

Give her that now. She's still in there, big personality and all, and she is worthy of loving herself exactly as she is.

I wrote this early in my own diagnosis journey, when the grief was still louder than the relief. If you want to see where that journey has led — into the family patterns, the marriage, the day-to-day repair — I wrote more about that in Attention Is a Relational Resource.

If this story felt familiar: whether you're sitting with a new diagnosis, an old grief, or just trying to understand your own brain a little better, therapy can be a place to slow down and make sense of it. You don't have to have it figured out before you reach out.