Jul 20, 2025
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The horrors (tummy ache) persist yet we (me my self and I) venture forth with the power of friendship (sprite saltine crackers and tums)
Sometimes when I get an ibs attack I pretend that its because my body is rejecting the human food as I am a vampire and can only feed off of blood.
Im trying to cope with my horrid “I be shitting” syndrome
Too much? Okay sorry my bad will go cry right now
this is another commission from tiktok it’s not complete yet, but this took me 5 hours and 24 minutes hope you guys like it :D
I'm an extremely low-maintenance goth so I have nothing but love for my HIGH-maintenance goth siblings, but I just finished hosting a spoken word night down pub and I'm tryna have an abysmal shit and all I can hear is *belt buckling up* *belt buckling up* *belt buckling up* *belt buc-*
Like, I am fighting for my fucking life in here can we speed it along Siouxsie Sioux??
my vibe.
Random chronic illness post because idk why not vent into the void?
I have heard, more than ever since starting my most recent job: “but you dont look _____”
And that phrase is going to make me crash out.
No, I dont look like your 5yo nephew with ADHD- I hide it *a lot* at work because I was raised in a school where I was bullied cause of it. I didnt have a choice. Ive had stims bullied out of me that only in the past year have resurfaced.
No, I dont look like I am disabled. Truth? Was out of school for 27 days cause of Covid, got POTS, have IBS, chronic migraines, and hypermobility. I hide them because I dont want others to feel uncomfortable even when Im trying to not die. People dont often see how my heart rate jumps to 110+ just from talking, how my teeth chatter cause I got out of the shower, how my nausea gets unbearable to the point that I sometimes cannot eat solid food without nearly throwing up, how im terrified to use my cane even when in the worst pain of my life—— fact is? Someone who ive considered incredibly close since- forever, has never seen me use the cane— I dont want to be percieved as though I am incapable of something even if Im dying— so I hide it—
And I dont if other chronic illness people can relate or not, but the chronic illness community has given me so much comfort for things that 2 years ago I would never have thought I needed comfort for— and I thank all of them so much