Yo whaddup :) I'm Sova Koopa. I usually just reblog a whole bunch, but sometimes I say a few things !!! Mostly my personal philosophies of life and such... content I reblog include Helluva/Hazbin, punk, hopecore, Super Mario, animal pictures, and any random thing I'm into at the time. I also love to talk and interact, so always feel free to do so with me :)
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The worst thing is that there is so much potential for exploring the horror of psych wards from the angle of medical abuse, ableism, forced treatment/drugging, loss of autonomy, power imbalance, demonization, dehumanization, etc, and YET the horror genre keeps defaulting to "insane asylums and psych wards are scary because there are mentally ill people in there"
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Me, doing my silly little crafts, trying not to fall into a hopeless abyss:
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Normalise Working in Bed!!!
A little note for anyone who needs a reminder they're doing what's best for them and that's okay!
ID in Alt.
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Happy Disability Pride Month!!!
Remember Folks:
- SELF CARE IS NUMBER ONE
- Use your spoons sparingly! Here’s some spoons to go: 🥄🥄🥄🥄🥄🥄🥄
- Clean your mobility aids! (Seriously dude when was the last time you wiped that shit down with an antibacterial?)
- Accommodate yourself, as others will follow.
- Make goals within your reach and abilities
- DO YOUR COPINGS SKILLS
- Remember to stay hydrated and take your meds!
- For my fellow heat sensitive homies, stay cool this summer! A cold rag draped behind your neck, airy clothing, a small portable hand fan, keeping ice packs ready, cold water and expecially cold electrolyte drinks, all do wonders!
- For my fellow autistic folks, don’t be afraid wear earmuffs, stim, use chew charms, whatever it is that helps you regulate. You don’t have to mask if it’s something that isn’t benefitting to your life.
- POTS havin mofos like me, salt the ever loving fuck out of your food. Try different foods with salt, such as fruits and vegetables! I’m currently eating a salty tomato. Drink lots of water, I’ve been aiding gateraid packets to my water and it’s made a HUGE difference, especially as someone who hates drinking water.
- Those with PTSD for whatever reason, I wish you safety and support as you learn to cope and hopefully heal.
- I don’t know exactly what to say to others with H-EDS, as I’m still understanding this disorder other then BE CAREFUL WITH YOURSELF THIS PRIDE MONTH. I swear to god we are the most accident prone mother fuckers lmfao-
- If your immune system is all fucky like mine, keep clean and be sanitary, communicate with others that if they’re sick you can’t be around them, and wear a mask if you feel like that’s the right option for you. In my hometown I’ve gotten yelled at more than once for wearing a mask post-covid, however you can’t let someone else’s ignorance result in your own suffering.
- Don’t forget to move around and stretch! A little movement can do a lot for your body.
- Check in with your disabled friends! Try and see if there’s any way you can help one another, see where both of your strengths and weaknesses lie, and swap some spoons!!
- Be aware of what triggers your disorders. Whether if it’s caffeine triggering bipolar episodes, the weather causing fibro flares, big changes causing meltdowns, overexerting your hypermobility, whatever it is, it matters. Listen to your body and mind.
- Don’t be afraid to call out that doctor who isn’t listening, dismissing your symptoms and medically gaslighting you.
- While it may not seem like a big difference for some, trust me when I say your appetite is so important! Remember if it comes down to it, that it’s better to eat something, ANYTHING, than nothing at all. 
- To that person who might be hesitant, ashamed or might be questioning wether or not they should use a mobility aid, if it’s the difference between you being stuck at home vs going out and living some life… USE THAT MOBILITY AID!!! Same goes for braces and any other tool that may help you live a better quality of life.
- Be accepting towards those with disabilities different then your own- remember this month isn’t a competition about who’s struggling the most, rather to understand that people of physical, psychological, sensory, neurodivergence, and even undiagnosed disabilities all share one thing in common.. WHICH IS BEING DISABLED!
- Doesn’t matter who you are, how young or old, black or white, thick or thin - the disabled minority is one you can end up becoming a part of at any time, and likely will if you live long enough. Disability doesn’t discriminate, so EVERYONE should be advocating for disabled people’s rights.
- And of course, have pride in being disabled. This shit is fucking hard, but if you’re reading this, you’re doing it. Just being here today and doing what you can handle or manage, is doing your best, and that’s enough. You don’t have to push yourselves to impossible lengths to be proud of yourself.
Here, have the disability pride flag:
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I 100% believe that the main reason people are scared they'll lose their creativity after they get help isn't because of some sort of self hatred most of the time, but because of the very material reality that the psychological industry exists to make people "normal" rather than happy. Like, when getting "help" means conforming to social standards, and your art is something that actively makes you less normal in the eyes of society, than it makes sense that you see that "help" as a threat to your existence as an artist. Most psychiatrists would openly admit that they'd consider turning an independent creative into an emotionless businessman as a win, why is it suddenly a conspiracy theory when the patient understands that just as well?
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Happy Disability Pride Month! This goes to the visibly disabled people, the invisible disabled people, the chronically ill, the mentally ill, the chronic pain patients, the chronic fatigue patients, any spoonie out there. You deserve love and care. You're worth it. You have value.
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big shoutout to disabled people who smell bad. disabled people who cannot shower regularly. disabled people who sweat a lot and it causes them to smell bad. disabled people who cannot apply deodorant due to mobility restrictions. disabled people who cannot do laundry regularly or at all, and end up wearing dirty clothes for a long time. disabled people who cannot clean their living space, and thus end up smelling bad themselves. disabled people who have any condition or disability that causes body odor. and any other disabled people who smell bad for reasons i didn't mention. i see you and i love you.
(this post is for all disabled people, including mental and physical disabilities)
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here’s to disabled people who can’t speak/struggle to speak. wether it be a physical thing, mental thing, or both, it’s okay. you’re not any less a person for it.
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Disability justice includes those who are disabled due to their own actions. You are not here to be blamed for what happened or why it did, you are here to receive love and support on your own journey.
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shout out to “gross” disabled people.
people who can’t shower/bathe people who can’t shave people who can’t wash their clothes people who need help going to the bathroom people who have nasty habits (biting nails, picking nose, etc) people who can’t brush their teeth people who can’t go to the doctor people who can’t clean their room people who can’t make their beds people who vomit a lot people who wet the bed people who constantly have diarrhea people who’s physical deformities are seen as repulsive
and every other kind of person I missed that deserves to be here too.
you are people, first and foremost. your thoughts deserve to be heard, discussed, acknowledged, no matter what. you are not lesser. you are just another person. you should never be ignored for what you can/can’t do. you deserve care.
to abled people: check yourself. make sure you listen. and you can reblog, just don’t derail. maybe don’t add on, either.
EDIT: reblog this version instead, please.
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special shout-outs to people who:
• won’t get better
• are terminally ill
• can’t be adequately treated/treated at all
• can’t afford treatment
• will die soon
• considered/are considering MAiD
• have problems that aren’t temporary
• have diseases that aren’t being researched
• are angry about being disabled/sick
• are sad about being disabled/sick
• are bitter about disabled/sick
• don’t want to joke about their sickness or disability
we’re still deserving of community
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D7 Fizz for @tali-zorah-vas-nerd
Long night with Asmodeus
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