I remember the red couch
too bright, too big, too red
its scratchy fabric pressing into my legs
as I sat beside Mum,
hands clenched in my lap,
while the air buzzed
with nervous stillness
that made it hard to breathe.
The lights flickered in that cold, clinical way,
and everything smelled faintly of paper and antiseptic,
like all the waiting rooms before
the ones where no one said what was wrong,
only that we were still “trying to figure things out.”
I didn’t know what to expect,
but I felt the weight of something coming
soft, heavy and slow,
like a storm inside my chest.
The psychologist’s voice was calm,
but her words echoed
down a long hallway
I hadn’t known I’d been walking.
Autism Spectrum Disorder.
Three words,
spoken like a sentence
but felt like a question.
What does this mean for me?
Why does this make so much sense?
Suddenly, without warning
everything shifted.
Not loudly or dramatically,
but like the sun after rain,
when the world feels damp
but warmer somehow,
and hidden things
start to show in the light.
I wasn’t just “too much”, “too quiet” or “too weird.”
I was a pattern named,
a song recognised,
a puzzle piece always there,
just not in the box others used.
But it wasn’t relief, not yet.
It was like being handed a map
to a place I’d lived in
without knowing its name.
That day became the starting point,
sending ripples through every future me
through friendships I’d struggle to keep,
through scripted conversations,
through the noise that made my ears burn,
and tags in my shirt that made my skin crawl.
It changed how I saw myself
and how I let others see me,
how I explained meltdowns,
how I forgave my need for quiet,
how I realized
I wasn’t broken
just different
Over time,
I saw the things that once made me feel outside
my love for animals,
my obsession with art and music,
my need for routine, space and silence
weren’t weaknesses to hide,
but strengths to embrace.
The red couch is gone now,
but it lives in my mind
in every quiet victory,
in every loud misunderstanding,
in every time I look back
and see how far I’ve come
from that little girl gripping her knees
on a too-bright couch
in a world she didn’t yet understand.
Because that moment,
that memory that clings tight,
wasn’t just about a diagnosis
it was the beginning
of learning how to live.


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