I grew up in a house where the air itself carried mood. The tension didn’t arrive, it accumulated. Like static, or damp. You didn’t always hear it in her voice. You felt it first. The way the cutlery drawer opened. The footfall across the lino. The time she took to answer when you spoke.
In the household of a divorced single mother and a teenage girl, my friends tried to protect me. They did their best. But when hypothyroid madness reveals coercive control and occasional physical violence, there is only so much anyone else can do.
Her circadian rhythm was inverted. She spent the night awake, listening to AM talkback radio filled with right-wing fundamentalist zealots. She slept during the day. I would come home from school to housework. Washing dishes. Making dinner. Feeding the dog and chooks. Then homework. She was nocturnal. I was trying to survive.
She wasn’t kind. Not always. Not in the cycle of abuse. Harm, remorse, promise. Repeat. She could be brutal, erratic, possessive. She could rage over crumbs, or fall silent for days. But no one explained why. There were no labels. No diagnoses. Just a quiet, continuous undercurrent of Serepax, one tablet three times a day, and warnings that lived inside me. Don’t push her. Don’t set her off. That’s just how your mother is.
I internalised it all. The weight. The guilt. The vigilance. I mothered my own mother. I built my personality around avoiding detonation. I built my armour around myself. Not always successfully. A single misspoken word could set off a tirade that lasted for days.
I didn’t complain about the soft drinks thrown at my face, or how sticky it is in your hair. I didn’t complain about the cigarette burns in the carpet. I didn’t complain at all.
Because I had learned: if you complain, you make it worse.
At thirteen, I stood in public phone booths in the rain. I called the GP. I knew the pharmacist’s name. I knew how long a Serepax script lasted. I didn’t know what the drug did. I just knew she needed help. And this was the help she had.
I watched her change, and then stop changing altogether. The woman who raised me was no longer rising. She was flatlined. Chemically and clinically.
Now, I know. She wasn’t mad. She was in endocrine freefall. She wasn’t too much. She was sedated out of herself. She wasn’t cruel by design. She was abandoned without a name for what was wrong.
It wasn’t her fault she wasn’t diagnosed.
And it wasn’t my fault I couldn’t fix her.
I had my own bout with hypothyroidism, caused by unrelenting and chronic stress in my thirties and forties. It was during that period, researching the condition, that I finally saw the full horror of what had happened to Lottie.
The swelling. The fatigue. The cold. The cognition. The rage. The utter loss of self. The flattening of personhood.
And then came the other truth. The one I couldn’t avoid.
When I was diagnosed with autism, so much of my childhood came into focus. The hypervigilance. The shutdowns. The mimicry. The freezing. The PDA, mistaken for a bad temper, became a spark to her petrol. The deep, urgent desire to fix things that weren’t mine to fix.
And I saw her more clearly than ever before. Not as a villain. Not as a martyr. But as a woman unseen. And then unrecognisable. Even to herself.
She should have been seen. She should have been tested. She should have been offered more than sedation. She should have been believed.
I am what the system didn’t get to do to her. I am diagnosed. I am angry. I am articulate. I am still afraid of the quiet before the yelling starts, but now I know the shape of it.
This is not catharsis.
This is not memoir.
This is forensic memory.
Her name was Charlotte Ford. She was born on 6 May 1920. She died on 19 July 2005.
Lottie. On this day, what would have been your 105th birthday – I see you.
You were worthy. You were always worthy.
But this damned patriarchal, misogynistic world let us both down.
This closes the three-part file for Lottie Ford. A case of medical misogyny, medical bias, and medical neglect.
This is not forgiveness. But, Lottie, I do understand.