disabled people should be allowed privacy. visible disability isn't an invitation to demand personal information from someone. and disclosing disability isn't an invitation to lay out each facet of that disability in excruciating detail. someone having a medical episode deserves privacy even if that episode happens in public. someone who is disabled and struggling or taking a break deserves to refuse people offering help without having to explain why. a disabled person who mentions some things about their disability but not every little thing is under no obligation to explain anything more than they already have. disabled people don't just deserve basic rights. they deserve dignity and grace and respect. and they deserve privacy
i know this won't be available everywhere, but especially if you live in a larger city where a lot of folks are affected by opioid use/addiction, it's a really good idea to ask local pharmacies, and even food banks if they are giving out free narcan (naloxone). this can also be found at certain behavioral health offices as well, my case manager is able to get them for me for free. narcan is a life saving medication that can temporarily halt an opioid (oxycodone, hydrocodone, heroin, fentanyl, codeine, morphine, etc.) overdose while you wait for emergency medical services to arrive.
opioid overdose is distress of the respiratory system, meaning that the person overdosing likely is struggling to, or can't breathe at all. it's very important to watch to see if the person is dealing with labored or shallow breathing.
here the official use guide:
[Image ID start: Two screenshots from the FDA's Narcan (Naloxone HCl) Quick Start Guide infographic. It reads:
"Narcan (Naloxone HCl) Nasal spray quick start guide. Opioid Overdose Response Instructions.
Use NARCAN Nasal Spray (naloxone hydrochloride) for known or suspected opioid overdose in adults and children.
Important: For use in the nose only.
Do not remove or test the NARCAN Nasal Spray until ready to use.
1.) Identify Opioid Overdose and Check for Response Ask the person if they are okay and shout name.
Shake shoulders firmly and rub the middle of their chest.
Check for signs of Opioid Overdose:
Will not wake up or respond to your voice or touch
Breathing is very slow, irregular, or has stopped
Center part of their eye is very small, sometimes called "pinpoint pupils".
Lay the person on their back to receive a dose of NARCAN nasal spray.
2.) Give NARCAN nasal spray
Remove NARCAN nasal spray from the box. Peel back the tab with the circle to open the NARCAN nasal spray.
Hold the NARCAN nasal spray with your thumb at the bottom of the plunger and your first and middle fingers on either side of the nozzle.
Gently insert the tip of the nozzle into either nostril.
Tilt the person's head back and provide support under the neck with your hand. Gently insert the tip of the nozzel into one nostril, until your fingers on either side of the nozzle are against the bottom of the person's nose.
Press the plunger firmly to give the dose of NARCAN nasal spray.
Remove the NARCAN Nasal Spray from the nostril after giving the dose.
3.) Call for emergency medical help, Evaluate, and Support
Get emergency medical help right away.
Move the person on their side (recovery position) after giving NARCAN Nasal Spray
Watch the person closely.
If the person does not respond by waking up, to voice or touch, or breathing normally another dose may be given. NARCAN Nasal Spray may be dosed every 2 - 3 minutes, if available.
Repeat Step 2 using a new NARCAN Nasal Spray to give another dose in the other nostril. If additional NARCAN Nasal Sprays are available, repeat step 2 every 2 to 3 minutes until he person responds or emergency medical help is received.
For more information about NARCAN Nasal Spray go to www.narcannasalspray.com, or call 1-844-4NARCAN (1-844-462-7226)."
End image ID.]
Do you think it's better to fail at something worthwhile, or to succeed at something meaningless?
“We all looked up” by Tommy Wallach
able bodied allies of disabled people when your disability genuinely has no secret upside and makes you useless to a late stage capitalist society
schizophrenia is not just experiencing positive symptoms (hallucinations and delusions). a lot of schizophrenics are neurodivergent in other ways. this focus on the positive symptoms is a villainious way to gatekeep us from neurodivergent spaces because our positive symptoms are typically portrayed as "scary".
our negative symptoms (flat effect, being withdrawn, avolition and anhedonia) are skewed to portray us as "evil" because we're not "emotive" or "caring" enough. schizospec disorders make everyday activities so hard. basic hygiene isn't a habit, we have little to no motivation to do basic things, the lack of happiness and pleasure can turn into severe depression for some of us and that's why depressive and bipolar schizoaffectives exist. people don't grasp the fact that schizophrenia is a disability.
i've personally experienced a lot of cruelty from other neurodivergent people because there is little to no education on schizospec disorders even within neurodivergent spaces. we're seen as inherently morally reprehensible for our disorder and people are so casually ableist to us. i'm not able to speak up for myself in these spaces because i feel like there is no where else i can go. neurotypicals are cruel to schizophrenics but so are other neurodivergent people. people need to have more care and love for schizophrenics.
yes that includes schizophrenics with little to no empathy, schizophrenics of color, trans schizophrenics, gay schizophrenics, schizophrenic systems, autistic schizophrenics, schizophrenics with adhd, fat schizophrenics, poor schizophrenics, homeless schizophrenics, schizophrenic sex workers, schizophrenics who've experienced abuse, schizophrenics with ocd, schizophrenics with ptsd/cptsd, schizophrenic children and teens, elderly schizophrenics, schizophrenics who are also physically disabled, all schizophrenics.
all schizophrenics deserve love.
I've been dealing with some of the worst pain of my life for the past 6 ish months. Knowing it could have been avoided if my pain doc had not decided to stop one of my medications is bittersweet. If she had only listened when I told her the pain was worse. But she didn't care. She simply told me to try not to think about it. I should have fought harder but I was so exhausted and dissociated. I've finally started treatment for it again, I just hope it works fast. I'm so tired...
I love spoon theory bc you can literally explain it exactly the same way it was originally explained, with actual spoons.
But also I feel like the failing phone battery is more accurate lately.
Like, you charge it all night, but it only slow charges. It never gets to full battery anymore.
When it says full battery, it doesn't mean the same as everyone else's, because it'll be gone twice as fast.
You have to limit your app usage bc of the battery drain, and even when you aren't doing anything the percentage is slowly going down.
Keeping it plugged in full time to charge means you can use your apps longer, but since it's slow charging it'll eventually reach 0 even when plugged in.
Keeping it plugged in full time also means the battery gets reliant on being constantly plugged in.
Actual percentages are a lie.
That shit will turn off with 5-10% battery still showing and there's nothing you can do about it.
The pain is more incredibly annoying than unbearable
24, they/them, nonbinary lesbian, disabled. Studying medicine, working on my internalised ableism, prioritising finding out what I like to do. I write, ish, or try to at least and that's something
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