[Image Description: Petch, a LEGO friends character with pale skin, brown eyes, and short brown hair. He is wearing yellow shorts, brown shoes, and a white shirt. There is a purple bag slung across his chest. One of his legs is a purple prosthetic. In the background is a partially visible black LEGO friends character wearing red pants and a green shirt. End ID.]
"Brain damage" only sounds like a harsh and offensive way to describe brain injuries because people constantly use it as an insult. It's a totally neutral descriptor of what it is. I have brain damage. My brain is damaged. It's not ableist to call it that, it's ableist to call people you don't like brain damaged because you think it's an inherently bad thing to be.
(Yes abled bodied neurodivergents, that includes you)
I don’t know if you’ve heard, but it has become a big conspiracy theory among teens in Tiktok the idea that Helen Keller was fraud that didn’t exist, and the main argument to back this is “how could someone be both blind and deaf and still be successful and write books”. That’s plain ableism. This entire thing is just deeply ableist and the fact that an ableist conspiracy theory like this can spread so easily among kids is just scary.
Conspiracy theories, misinformation, fake news and bigotry are not a generational thing! It’s not a “boomer” thing, this is something that happens among all generations.
*mom voice* You can get these words back when you know what they mean
another mental illness meme i made out of boredom
I feel like people forget that pediatric illnesses generally last into adulthood like…childhood cancer survivors often have medical complications for the rest of their (adult) lives. My juvenile arthritis will be around when I’m 75. Crohn’s disease, cystic fibrosis, congenital heart defects - all of these things, when acquired in childhood, have lifelong complications. Childhood diseases aren’t just cute, happy kids smiling from hospital beds. Theyre pain and suffering and learning to live differently forever.
I have ME (myalgic encephalomyelitis) also known as chronic fatigue syndrome. People seem to think that it's just that I'm a bit tired and i often get comments like "I'm tired too" or "i think I've got a bit of that".
Most people fail to understand the differences between fatigue, chronic fatigue and chronic fatigue syndrome (ME), so I'll explain:
Fatigue is extreme tiredness caused by mental or physical exertion or illness.
Chronic fatigue is extreme fatigue that doesn't go away with rest and last for a long period of time usually due to a chronic illness. While not an illness in itself it is a symptom of many chronic illnesses.
Chronic fatigue syndrome (ME) is a chronic multisystemic neroimmune disease (meaning it affects a lot of stuff and lasts a long time). While chronic fatigue is the most well known symptom it is not the only one. ME/CFS can cause a wide variety of problems including but not limited to, sleeping issues, cognitive functions, muscle and joint pains, headaches and migraines, soar throat and glands, flu-like symptoms, dizziness and feeling sick, breathlessness, hypersensitivity and heart issues such as palpitations. ME/CFS can last anything between months, years, decades or even life. No matter how much you rest it doesn't go away. There is no cure and no effective treatment. It is NOT just tiredness!
I have soul crushing chronic fatigue that you probably can't even imagine and it plagues every moment of my existence. I am in constant pain. My clothes hurt my skin, the light hurts to look at, the sounds make my migraines worse. It hurts to move, if i so much as breathe it feels like I'm being stabbed a thousand times. My brain no longer works correctly, i have brain fog all the time. I can't sleep no matter how badly i need it and when i do it's filled with nightmares and i wake up at 3 in the morning crying from the pain. Even if i had the best sleep of all time i would still wake up the same, more sick than i previously thought possible.
So I'll say it again,
hi, sorry to be on anon but i recently realized im a klepto and looking through the tag you seemed nice. i was wondering where you meet other kleptos online? like without getting like triggered (if thats the right word) or just a bunch of puns smh
Yee fucking haw, I get to write something again. Hi internet people, tis I, Ko, the reoccurring guest speaker. I think this is my...third? post. Something like that, but ok, answering stuff time. Hey, no worries being on anon, it's there for a reason right? I seem nice...but it's a trap! Jk, I mean, I try to be nice, but does that go well? It's a mystery.
Ok, so I've never actually seen an online space for kleptomaniacs in the wild. I did a little search thingy on discord and the relative rest of the internet (I don't have facebook so I didn't check there) and 99.9% of all of them were lifter bullshit, saying stuff like "Omg, I'm such a klepto" *shows off intentional shoplifting haul*. So yeah, not totally a great space. Like, not trying to start shit, but lifter community, quit using the word klepto. I don't wanna be associated with you when you get arrested. If you're stealing for the point of showing off, and not because of a mental disorder or a genuine need, I think you gotta take a good look at yourself.
So this is going to sound pretty sucky, and I feel bad for having this as my general answer, but I think kleptomania is going to be one of the rarest communities to find. There's a lot of shame associated with the disorder, (I'm sure you know, I'm just tossing general facts out there for some odd reason.) and like I for one try not to talk about it unless I'm asked like I am now, which is totally cool. Anon, no self doubt allowed, I'm glad you reached out and you seem like a chill person. Basically what I'm saying is that I'm pretty sure there's not really an open community for kleptomaniacs that's free of triggers and puns, just because no one really sits down and talks about the realities of it. Real talk though, I hate the puns. Like if someone's first reaction to hearing that I'm a kleptomaniac, idk, I will be sad and annoyed XD
So yeah, sorry, this totally isn't a helpful answer, buuuuut I will totally one hundred percent keep my eyes open and ask around to the few other kleptomaniacs I personally know, kay? For now I'd keep scrolling through the tags like you are now. It might take a hot second to get through the bullshit, but I'd bet money that there's at least three good people out there. And hey, if you have any questions or just want to vent, I'm here for you I guess XD-Ko
To my knowledge, my hair started turning grey when I was ten. But, from what I remember, I was super surprised to find a grey strand so it might have started sooner than that. My hair has also steadily been getting greyer since then.
It's ME awareness day and next week is ME awareness week, so here's a post about ME that you may find interesting or helpful!
I have ME it's one of my diagnoses, and I struggle with it on the daily! I wish more people understood how my body works and feels but sometimes the best I can do is a post like this
Anyway enjoy!
ID in Alt
give me a show with disabled queer representation. and I don't just mean amputee that is not affected at all by their amputation because "we're all basically the same- woo friends!". I don't just mean non descript wheelchair user that uses a hospital wheelchair. give me young queers using canes and rollators and white canes and powerchairs. and give them bright hair and make them neurodivergent and have struggles in life relating to them not fitting in with a lot of abled queer representations and "disabled friendly" pride events that aren't disabled friendly. make them black, make the Asian, make them fat, make them interesting. make them angry, make them punk, make them pastel, make them have interest and passions, have them protest, show them taking breaks and having to take care of themselves. please.
Raven, he/him, 20, multiple disabled (see pinned for more details.) This is my disability advocacy blog
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