They fly across my mind like paperwork
I've rehearsed handing over conditions I've read about at three in the morning,
But they don't hear that part.
They see a girl in her 20s
who had a baby too young,
who speaks too carefully,
who chose today, of all days—
They tell me I'm not unique.
They don't say it cruelly.
They say it like reassurance.
Like permission to minimize.
Everyone has mood swings.
Everyone gets overwhelmed.
that says I swear I'm not lying.
where I recognize I deserve better,
where survival feels negotiable,
where I still have the energy
before it disappears again.
They don't chart that part.
They condense my days into bullet points.
Prescriptions for the loudest symptoms—
the ones that interrupt their schedule.
Everything else becomes background noise,
the list starts to feel fictional.
If no one can hold it all,
Maybe I'm just bad at being alive.
No doctor sits long enough
to hear what happens every day,
jaw clenched so tight my teeth are cracking,
the moments where my body
refuses to cooperate without explanation.
I can describe it perfectly.
But if they don't see it,
So I stand at a crossroads
that no one acknowledges:
keep writing about the things
I don't understand and can't fix,
or fight tooth and nail for a diagnosis that might finally make me legible.
Writing doesn't require proof.
It doesn't tilt its head at my age
or the way I learned pain too early.
Because if I keep fighting,
until the very last moment,
until something undeniable appears,
How many times can I survive being misunderstood before it costs me more than the answers are worth?