almost home
Mike Driver
Jules of Nature

Product Placement
Not today Justin
noise dept.
art blog(derogatory)

gracie abrams
cherry valley forever
he wasn't even looking at me and he found me
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PR's Tumblrdome
macklin celebrini has autism

Andulka
PUT YOUR BEARD IN MY MOUTH
The Stonewall Inn
EXPECTATIONS
Sade Olutola
seen from Germany
seen from United Kingdom
seen from Italy
seen from Germany
seen from Italy

seen from Switzerland
seen from United Kingdom

seen from United States
seen from United States

seen from Malaysia

seen from Germany
seen from India

seen from Türkiye

seen from Singapore
seen from Colombia

seen from Switzerland

seen from Singapore
seen from Germany
seen from France

seen from Ireland
@potsiepumpkin

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me trying to exist: sitting down calmly reading
my heart rate: I think 120 is appropriate for this situation
Me: stands up
My heart rate: 150 must be to correct response to such an egregious action
✨Reverse Gaslighting✨
little miss awful body temperature regulation is taking his hoodie off again
little miss awful body temperature regulation has put his hoodie back on
disabled clown: oh boy I made it home! As a treat I’ll put on my compression socks and my compression belt and my compression shirt and my compression handkerchief and my compression handkerchief and my compression handkerchief and my compression handkerchief and my

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Ok but can we talk about the loneliness that comes with being chronically ill? If you’re not able to work or go to events, there’s so much time spent by yourself.
It feels like Im a zoo animal with no enrichment or friends, just me staring out the glass
Putting on icy hot and then getting under an electric blanket to create a sensation I’m calling ~spicy room temperature~
Like, I’m clearly not well.
Blood tests came back abnormal, proving that I was right and my family was wrong!
And that I did not, in-fact, just need to change my attitude, think positive and move around more.
some days I think my pain has grown less
and then other days I’m convinced that it hasn’t grown less, but rather I’ve just grown much more used to it

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When the brain fog kicks in..
I think I found the limit on the amount of medication my doctors can put me on. I can’t stand the side effects anymore.
absolutely hate it when I wake up tired like what the fuck did I lie unconscious for
It bothers me so much that the healthcare system relies so much on the patient's ability to advocate for themselves, organize their history, and be so persistent against every medical “professional” who says there’s nothing wrong/they can do. But so many struggle with fatigue, brain fog, and face such ingrained systemic barriers, that the people who need and deserve help and support can’t access it.
I saw something recently that resonated with me: “Access shouldn't depend on who has the energy to fight for it.” And I’ve never agreed with anything more.
babe are you okay you reblogged got that fog in me 11 times
wait, i did? i don't remember doing that...

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If I could broadcast this message everywhere I would. This is exactly what is happening.