Two new LEGO friends characters, Petch and Ida, are disabled. Petch has a prosthetic leg (purple and it's an above-knee prosthetic) and Ida is, based on appearance, a, person with albinism. I am so excited to see more of these two in the future!
I I think I mentioned this before but can't find the og post so I'm just gonna talk about it again.
I want people to understand that not all pyromaniacs are anarchists, not all anarchists are pyromaniacs and pyromania and anarchy do not go hand in hand.
I would much prefer if people would stop portraying every anarchist character as a pyromaniac esp cuz they're not actually doing acts of anarchy nor portraying pyromania properly. They're just burning shit and yelling "fuck (in-story mega corp here)"
That said, I am proud of actual pyromaniacs (and pyrophiles) who are anarchists. Because I too wish we could dismantle capitalism and shit.
Just please dont go around burning property and crap in the name of anarchy, regardless if you have pyromania or not, a crime is still a crime and there's enough parts of the world burning to the ground and purring people and general life in danger right now.
Pyromania and anarchy do not go hand in hand, do not make these your characters only/defining traits. Please.
Ones a movement/belief system, the other is a fucking condition.
*guy with an undiagnosed disability voice:* haha it’s kinda crazy how everyone just deals with the constant unending pain but we just keep trucking per usual 💯💯💯
My cousin is noncompliant diabetic (type one,) but not by choice.
So, she's six. Her parents do not listen to her doctors and will not follow her diet plan. She stays part-time with another one of my cousins and he does his best to follow her diet and make sure her needs are met, but he doesn't have her at all times. There have been a lot of times where she gets dropped off at his house only for him to pretty much immediately need to take her to the ER because she's in ketoacidosis or her blood sugar is extremely off. There was one time where things got so bad she was in the PICU on a ventilator because her lungs stopped working, it was a miracle she survived and he's worried that it will be too late if nothing changes.
I don't know. I'm just worried about her and I'm venting about it. There's no way to help her without trying to go to CPS, but there's no family in the immediate area if she gets removed from the house who can take her and if they don't take her, her parents might retaliate and move somewhere else or stop letting her stay at my cousin's and then she's in even more danger. I wish I knew what to do. She deserves better than this
y’all, this is a gentle reminder that radqueers are not welcome on our blog. this is not the space for you. in order to help keep our blog a safe space for disabled people, people of color, abuse survivors, transgender people, and other marginalized groups, we ask that radqueers please do not interact. if you choose to continue to interact with us, know that you are disrespecting us and crossing one of our personal boundaries.
we have explained some of the issues with a few radqueer identities in this psa:
if you are transx/transid/radqueer, we can’t stop you from interacting. but please know that you are crossing our boundaries by being here, we are not comfortable with you here, and our posts have never and will never be created with radqueers in mind. and remember, endogenic systems have never been, and will never be, inherently radqueer. many endogenic systems have always and will always exist outside of the radqueer community.
so sorry to our followers who don’t want to see posts like this. we’ve been getting some radqueers in our notifications lately so we thought this message bears repeating. thank you for listening and respecting our wishes. take care.
"i'm using delusional in the right context, it's not like it's that serious"
DELUSIONAL DISORDER + SCHIZO SPECTRUM DISORDERS + TBI + MANY OTHERS
"calling someone a narcissist isn't ableist it's not a disability"
NARCISSISTIC PERSONALITY DISORDER
"sociopath/psychopath are just adjectives it's not like I'm hurting anyone"
ANTISOCIAL PERSONALITY DISORDER
"saying i'm ocd doesn't affect you it's just the way i act"
MOTHERFUCKING OBSESSIVE COMPULSIVE DISORDER
OBSESSIVE COMPULSIVE PERSONALITY DISORDER
"i'm schizoposting lol it's just a joke"
SCHIZOPHRENIA
SCHIZOID PERSONALITY DISORDER
SCHIZOAFFECTIVE DISORDER
SCHIZOTYPAL PERSONALITY DISORDER
it's never just a joke, it's never an adjective. use a fucking thesaurus
shout out to the disabled people with emotional dysregulation particularly in regards to anger. people who get overwhelmed just by feeling things, people who don't know how to direct their strong emotion so its directed inwards or outwards indiscriminately. people who hurt themselves or break things, especially things they don't want to. people who start crying when they're angry and hate that people treat the anger less seriously as a result. anger is considered monstrous sometimes, like some sort of failing when it's just one emotion out of many. people act like if you can't control your anger you're automatically an abuser who exclusively and specifically takes their anger out on other people. there are indeed many instances where someone needs to learn to regulate their anger, but i'm talking about strong emotion in the context of disability. where just the act of feeling is too much, where people don't have the capacity to process their own emotions, and how difficult that can be
please please please don’t forget to include intellectual disability, psychosis / schizospec disorders, level 2-3 autistics, folks w dissociative disorders, and others with “severe mental illness” from ur conversations about mad liberation.
these are some of the most vulnerable and disenfranchised mad people, and we need to give them a voice.
these are the places where liberation is needed the most
A list of pyromania symptoms one might experience.
Not a guide to diagnosis.
- the urge to ignite flames.
You most likely will feel the urge to start fires in some way, be it activating a lighter repeatedly or creating bigger flames by burning things. The urge can feel like an itch in the brain, a stretch in your fingers or just the sudden need to grab a lighter or fire source. It can be very intense at times, making it hard to resist the impulsion to do so.
- the urge to touch flames
Some experience the impulse to attempt touching fire. From putting your fingertips to a candle or lighter flame to putting your hand on a campfire or bonfire. This of course is a pretty dangerous and possibly self harming urge to have but the majority of the time the intent isn't to harm but simply to feel the warmth and sting of holding fire.
- satisfaction in fire
Many feel relief, relaxed or even euphoric once they've started fire. For many, fire is a sort of stimuli almost nothing else can give them. Watching a small flame dance or watching fire eat away ant kindling can be enough to satisfy the crave in their brain for that stimuli, however for some that still won't be enough, thus why the most commonly known pyromaniacs tend to be people who create much bigger fires than anything.
- stress or depression
More often than not you may feel mood swings due to the lack of stimuli your brain craves from fire. Going without it for long can cause some sort of distress that manifests differently for everyone and can become more intense the longer you are letting your brain crave to give in to the impulses. For some this comes as a depressive episode, high stress levels, anxiety episodes, paranoia and so on, often influenced by any possible conditions one might have in addition to pyromania or simply influenced by their environment. This can cause someone to lash out, isolate and shut down or even lead to them creating a bigger fire to relieve all that distress.
- lacking control
When struggling with an impulse based disorder like pyromania, you may experience a lack of control over your impulse, starting fire and lighting things without thought and being quick to give in to urges. For some this lack of control can be small, they are able to resist the impulses better than others, but for some this lack of control is large and they struggle intensely with the urge to start flames.
- feeling drawn
Many feel obsessed over or lured to fire and flames, an almost intense affinity of some kind for all things related to fire.
- purposeful sparks
Most fires pyromaniacs set are on purpose and if you have pyromania you likely experienced setting more than one or two fires on purpose.
- excitement
Plenty feel a rush of some kind just before starting a fire, almost a thrill in the anticipation or excitement at the idea of the act. Some feel this as glee towards the relief fire gives them. Very rarely is this ever sexual, if it were it would be pyrophilia, a different condition.
- hoarding
Some collect fire related materials like matches and lighters or candles due to their fascination for fire and always feeling the impulse to start one. Some may carry a lighter at all times just to watch the flame in small moments when the urge starts bothering them during the day. It's not uncommon to find a lot of candles or different lighters in there home in varieties, often a range of used, empty or new lighters. Some even keep all their lighters instead of throwing them away after they've emptied.
Unfortunately there is still a lot of research yet to be done about pyromania, it's causes and it's symptoms as it is not a very common disorder to have. Some even call it rare.
This does not mean that very little is currently known, plenty is known about the disorder so far and I intend on sharing as much as I can and making the knowledge as publicly available for free as possible, but there is quite a bit still yet to know.
I'm sure there are symptoms I missed for example.
While I have the disorder myself I am not a professional, nor in the medical field, and so there is much I myself may miss.
While I'm not an expert, I am open to answering questions and discussing as much as possible.
@clusterrune @delightfulweepingwillows @hewasanamericangirl
Not going to tag a very icky post that I found but it’s not hard to find. So, here’s your reminder that;
Self suspecting and self diagnosed autistic people are NOT taking resources from diagnosed people. You can’t get autism services without a diagnosis, you can’t go to any therapies really without a diagnosis and so on.
Autism accessories have a abundance supply. So yeah, get those ear defenders, get those sunglasses, get those stim toys.
You aren’t taking anything from diagnosed people.
Stop saying self diagnosed people are taking away from diagnosed people, because they’re not. They have their space in the community. The community is big enough for them.
When I talk about visible autism on my blog, I’m usually not talking about those who are clocked as quirky and weird. Although that’s completely valid, I’m not talking about them. I’m talking about those of us who are VISIBLY autistic. Those of us who are clocked as those autistics. Who are clocked immediately as having something wrong with them. Those of us who are named as slurs. Who are yelled at. Who are attacked. Who are glared at, pointed at, stared at, pitied. Those of us who are automatically assumed to be with caregivers. Those of us you see talked about in medical journals and on the news as “inspiration” when we graduate or get invited to prom.
This is us. This is who we’re marked as. This is who we are seen as. We are seen as less than, as animals, as objects, as “inspirations”. When we accomplish something it’s usually not seen as our accomplishments but as the accomplishments of our caregivers and support staff.
I get so mad when someone comes onto my blog, MY blog. Me. A visibly autistic, nonverbal person, and doesn’t even look at my tags or pinned post and says “Omg me too, I’m seen as quirky and awkward, I’m visibly autistic 🥰” and like…go you but I’m not talking about you. I’m not talking about “low masking”. Im talking about LOW masking. No masking or very very low masking. Those of us who are immediately seen as autistic.
And it’s frustrating. It’s frustrating when people come into my blog and say this because, you DON’T get it. You just don’t. You don’t get what my life is like, what my experiences are. What it’s like to be LOW masking or no masking. You don’t get that. And yet you try and squeeze yourself in. And that hurts. It hurts to have people who won’t ever understand this squeeze themselves in. Stop doing this.
Raven, he/him, 20, multiple disabled (see pinned for more details.) This is my disability advocacy blog
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