What I'm still seeing With Out eyes, part 2.
Chapter 4
Last night, the reddish-orange light was so bright, so
intense, it filled everything. I couldn’t even tell when I’d closed my eyes—the
usual dark reddish-brown I expect was nowhere to be found. It was just light,
bold and burning, like a fire behind my eyelids.
By morning, the world inside me had settled. The brightness
faded back into its usual heavy grey, with slow-floating yellow shapes drifting
through the fog. And now, as I sit quietly, the darker reddish-brown edges have
returned—faint but grounding—like the calm after a storm.
Right now, I see yellow floaters swimming lazily through
that grey space, with a soft peach tint in the background. It’s quiet, gentle,
almost dreamlike.
People ask me, “What are you up to?”
It’s a casual question. A way to check in.
And I answer casually too—“Oh, just chilling. Writing on my disability page.
Sipping some coffee.”
It’s true, but it’s not the full truth.
What I don’t say is that while I sip that coffee, I’m
watching yellow floaters drift across a grey world inside my mind. That
earlier, I was trapped in a blinding reddish-orange light so intense I couldn’t
even see the darkness behind my closed eyes.
I don’t say that I push it all to the back of my mind when
I’m around people or on the phone. That I keep it to myself because it’s easier
than trying to explain. Easier than seeing their faces twist in confusion, or
hearing the long pause on the other end of the line.
So I just say I’m chilling.
And despite all of it, I’m still so grateful.
Grateful that I have the mobility to do the things that
matter. I can load the dishwasher, unload it, take care of my elderly grandma
the best I can, clean my room, carry my laundry downstairs, and put it away
when it’s done.
I’m still able to socialize with people, to have real
conversations. I can still listen to the birds singing outside my window, even
if my hearing’s not perfect. It’s not great, but it’s enough—and I’m so
thankful for that.
It’s the little things. Family. Friends. The simple ability
to do what I can. I hold onto those moments tightly. They keep me grounded when
everything else feels like it’s floating.
Just now, I helped my stepdad bring some garbage down.
It might sound like nothing, but to me, it meant everything. I felt proud of
myself. Proud that I could help. Proud that I could move through my space, take
action, and contribute.
Moments like that remind me that I’m still capable—still strong—still needed.
And that pride? I hold onto it. Because I’ve earned it.
I’m also still able to hear things that bring me joy—like
the sound of rain falling, thunder rumbling in the distance, or cars whooshing
by outside my window. I notice the birds each morning, singing their songs. I
hear the soft cooing of doves. These sounds aren’t just background
noise—they’re part of how I experience the world.
Even with my hearing loss, I can still catch these moments.
Not perfectly, not always, but just enough. And for that, I’m forever grateful.
It’s just like I’ve been telling you — I’m totally blind,
with no eyes. Yet, somehow, I still see colors and shapes inside my mind. This
internal sight is vivid and real to me, even though no one else can see it. On
top of that, I have high-frequency hearing loss, which makes it hard to hear
important sounds like cars when I’m trying to cross the street. The background
noises get loud and mixed up, and it’s confusing and scary.
This happens during the daytime too. When someone is
talking, I can’t always tell if they’re actually saying “Kamala! Kamala!” or if
it’s something else. I think that’s because of my hearing loss. But when
someone really is calling me, I often don’t hear it—maybe because I’m focused
on something else, or it’s loud, or the door is closed, or I have headphones
on. That’s normal and makes sense.
But at night—that’s when all the craziness comes in. The
quiet and darkness seem to bring out these confusing sounds, and it feels like
my mind is playing tricks on me in a way that’s hard to explain. Sometimes, I
think I hear someone knocking on my door when the whole house is asleep, or I
hear voices talking when everything is completely quiet. How is that possible
when my hearing is damaged? These sounds blur the line between what’s real and
what’s inside my mind, making everyday life even more challenging.
Having a hearing loss makes talking on the phone hard for me
too. When I’m on my iPhone, I have to have it laying right in front of my eye,
and the volume has to be loud enough so I can hear it clearly. If the phone is
even a little bit away from me, it still sounds like it’s far away—even if the
volume is turned up. That makes phone conversations tiring and frustrating.
When I’ve tried to explain this to people, they often don’t
understand. They say things like, “What’s wrong with you? Why would anyone be
calling you? I’m just playing my game,” or, “People are sleeping.” It feels
like they think I’m imagining things or making it up. So, I end up saying I’m
“hearing things,” but really, I wish they could understand the confusing
reality I live with every day.
Sometimes, these experiences make me wonder—am I dreaming
even though I’m not fully asleep yet? Or maybe I’m asleep but don’t realize it,
thinking I’m awake when I’m really somewhere in between?
It’s hard to tell, and that uncertainty adds another layer of confusion to my
day-to-day life.
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