Potsie Pumpkin @potsiepumpkin - Tumblr Blog

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

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✨Reverse Gaslighting✨

#chronic illness #chronic pain #disability #pots syndrome

infectiouspiss

little miss awful body temperature regulation is taking his hoodie off again

infectiouspiss

little miss awful body temperature regulation has put his hoodie back on

daveagainstthemachine

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

nimandmossy

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

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electric-lavender

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.

#chronic illness #chronic pain #disability #pots syndrome #spoonie #chronically ill

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.

#chronic illness #chronic pain #disability #blood tests

vaticrevelation

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

swoony-spoonie

When the brain fog kicks in..

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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.

#chronic illness #chronic pain #disability #spoonie

autistobrat

absolutely hate it when I wake up tired like what the fuck did I lie unconscious for

miinobobeano

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.

memewhore

ihavenohotcocoa

babe are you okay you reblogged got that fog in me 11 times

catgirlanarchist

wait, i did? i don't remember doing that...

#brain fog

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

#chronic illness #chronic pain #disability #medical tiktok #pots syndrome #chronically ill

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fibro-memes

themysticmango23

Chronic illness is so isolating because I am curled under a pile of blankets trying to sleep while my body kills me and my family is laughing in the living room and I can hear it through the walls but I cannot reach them

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