Okay, here's my attempt at an #introduction!

Heya, I'm Fermata! I'm a demisexual mostly cis AFAB late-30s person who's been on the Fediverse for a long time. This is an anonymous alt account; my main account is elsewhere.

I'm here to talk about my #writing projects, and possibly about fandom stuff as well. Writing-wise, I'm working on an erotic Regency romance story, 80% of which is hella gay.  It doesn't quite have a working title yet, so I usually just refer to it as my "regency romance" or my "gay romance" story. I'll write a bit more about it in a reply for anyone interested.

Fandom-wise, I've gotten really into Japanese #otome visual novel games. :3 They're often silly and self-indulgent, but they also feature some excellent stories, wonderful characters, and a lot of heart. Favourites so far include #EvenIfTempest, #JackJeanne, and #VariableBarricade.

I'm also an #artist, and I'm only just starting to dip my toes into drawing smut/erotica/porn, so you may see some of that here, too. It'll likely be art of the main characters of my writing projects, but who knows where I'll go, haha!

EDIT: Oh, and I should also add: I'm #ChronicallyIll with an energy-limiting disease.  

So that's me! I'm excited to have a place to chat about my writing, blorbos, and other romance/erotica-related silliness. Feel free to follow, but make sure you're over 18.  

My AO3 account: https://archiveofourown.org/users/QuietFermata/works

#Introductions #Intro #long

QuietFermata - Works | Archive of Our Own

An Archive of Our Own, a project of the Organization for Transformative Works

That was fun. Started feeling lightheaded and woozy. Think I will be horizontal for the rest of the day.

#ChronicallyIll

I spent this afternoon lying on the floor, too dizzy to sit, stand or walk. But I still forced myself to work (until I fell asleep... on the floor). One day maybe I'll learn how to actually rest. Hope so.
#chronicallyill #disabled #writer

Waiting room talk (in German):

„Maybe we should go to work.“ (instead of wasting time in the waiting room?!)

Me: „I can't work, unfortunately.“
„But you are still young.“
Me: „I am chronically ill and disabled.“
Looks me up and down. „I'm sure you can do something.“

And it kept going like that. Two able-bodied men explain to me that I am healthy enough to work.

#disabled #chronicallyIll

Wobei ich mir dann auch wieder denke: So schlimm ist mein Körper gar nicht. Eigentlich ist er - unter den gegebenen Bedingungen - bewundernswert. Er hält das alles aus, beißt sich da durch. Er trägt mich bis jetzt durch den ganzen Scheiß. #chronicallyIll
Spent the day upcycling an old hoodie to give it some new life 🪡🩷 I had a totally recharge day, which I really needed 😮‍💨 My body is working overtime at the moment, so days where it can just recharge are very important 🩷 #sewistsofinstagram #upcycledclothing #chronicallyill #chronicillness #mentalhealth #schizophrenia #adhd #cptsd #trauma #depression #ootd #anxiety #recovery #psychology #mentor #recoverymentor #redhair #fashion #fashionphotography
#sew #sewing #homemade #lovesewing #syning #upcycled #hjemmesyet #syguide #syet

Me: Yummy skyr with mirabelle jam and banana?
Stomach: sounds gooood!

Five minutes later, skry bowl in hand.
Me: Oh that looks so good!
Stomach: I'm noping out. You really thought you could eat breakfast?

#chronicallyIll

"'You'd get better if you just....' is bullying and we don't deserve it." by K. Johnstone

https://substack.com/@mecfs/note/c-203079885

Screenshot from AMMES May 2026 Newsletter

#chronicillness #ChronicallyIll @longcovid
#LongCovid #MEcfs #PwME #ME #MyalgicE
@mecfs

crows_trinket_trove - Twitch

happy pride, let's play Coral Island! | Spring, Year 1 | !lurk friendly

Twitch

Reading an article on craniocervical instability in Ehlers-Danlos Syndrome, and its again connecting some symptoms logically, and it would be so nice if I had any kind of medical guidance. Instead, I have read scientific articles on my illness all the time to understand things.

I've had back pains since my youth. It's so fucking ridiculous that I always have to figure out everything myself.

#EDS #chronicallyIll