Cosimo Galluzzi
cherry valley forever
I'd rather be in outer space 🛸

Janaina Medeiros

@theartofmadeline

JVL
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Sweet Seals For You, Always
2025 on Tumblr: Trends That Defined the Year
trying on a metaphor

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祝日 / Permanent Vacation
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@chronicillnessmemes

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"why do you always talk about carrying narcan with the same memey tone as ibuprofenposting? like what is this bit, what are you doing" 1. I am actively trying to make it seem like an easy, normal, and non-intimidating thing to do. which it is! a lot of people have access to naloxone but don't think to actually get any because they think they don't have a reason to need it, but if they just saw three memes about being a narcangirl then next time they see some on offer for free to the public then they might remember "wait. I'm the public. I, too, can be a narcangirl." 2. this isn't even a bit for me I am genuinely like this. me and my narcan #mynarcan
Happy pride month! Please remember to include disabled people in your festivities this year! This includes:
- Hiring sign language interpreters
- Ensuring venues are step free
- Making dedicated sensory safe spaces
- Providing free masks
- Including braille or audio described signage
- Using plain language in speeches
Yes it’s more work, but pride is for everyone, it’s needs to be inclusive.
they really don't respect the time of disabled people. your application can take up to 12 weeks. the specialist waitlist is 3 years. your assessment will be any time within the next 6 months. let us know if you cannot attend this appointment you waited 7 weeks for and we'll reschedule next year. we've decided to assess you at this time and day and you have to be available or any support you dared to apply for is not going to happen. and in between these long bouts of waiting you have to survive the everyday
the really crazy thing about cooking is that once you practice it enough (for all the gamers reading this: "grind enough exp") your threshold for wuat counts as a low effort / depression / I Dont Really Want To Cook meal rises steadily and you can feel yourself becoming the kind of person whose "chill dinner" takes 1h45 and involves three pans
ok but how do I get there from "assembling a sandwich is too much work"
As someone who went through this and struggles with chronic pain and fatigue, add 1 thing semi regularly. And I do mean just 1 thing.
When I first moved out most my meals were instant ramen. Then I started adding 1 egg to that ramen to get a little protein in. In a couple months, 1 egg became two. Then it was 2 eggs and 1 chopped green onion. Then a couple months later I was adding carrots and other vegetables. In about two years I was able to skip the instant ramen part altogether and now use chicken broth and noodles and I’m basically making a ramenesque soup from scratch when I’m craving ramen. It took 2+ years total of just gradually, one at a time, adding one ingredient. Over a period of months/weeks.
Start with where you’re able. If a sandwich is too much, maybe try just a piece of bread and some meat or cheese. Focus on where you can be gradually introducing more nutrients into your body. 1 slice of deli meat. A couple weeks later, that plus 1 slice of cheese. Then 1 vegetable. Maybe they don’t all make it into sandwich form and that’s ok. But if you keep what’s the most basic and simple for yourself and slowly add 1 thing that’s not too much of a hassle, over a couple months you might start toasting the bread before putting cheese and meat on it. Then one day there’s more vegetables. Years down the line you might find yourself owning a panini press or slicing your own bread.
Most of us will never be gourmet chefs and that shouldn’t be the goal. You might not ever get to the point where you own a panini press. But the more important thing is that you’re finding ways that work, for you, gradually, in order to make your meals more nutritious. The expectation to cook a full, unique meal every night for dinner is a relatively new phenomenon and completely unrealistic for most people. Having the same 3 things you can make consistently and keep on rotation is plenty fine, especially if you get to the point where you can mix it up a little bit by adding ingredients in the method stated above. Feeding yourself should be the #1 goal, getting more nutrients in #2, and stepping it up to the next level #3 when you have the capacity to. Like with a lot of things, it’s really just about consistency. Start with where you can be consistent. If that’s 1 meal a week you cook yourself and the rest is hot pockets, but you can do that 1 meal consistently, then that’s where you start. Then when you have that down, maybe try two (of the same) meals a week, or ask what you can add to your hot pocket to make it a little better for you. (Some vegetables on the side for instance).
Don’t try to jump in from 0 to full course meal all at once or you’ll overwhelm yourself. Building a meal outward from bread and butter over a period of weeks is incredibly possible. No two peoples’ timelines will be the same, but it is entirely possible and that success will look different for everyone, and that’s also ok. As long as you’re feeding yourself, that’s what’s most important.
this is so helpful. too many times when I ask how to do something, people tell me to "just do it" like I'm supposed to already know what steps to take. and I almost never know what steps to take. someone actually telling me is so refreshing
My advice for getting from "sandwich too hard" to "can actually cook, somehow" is to get a rice cooker, start messing around with what liquid you cook the rice in, start adding stuff to the rice while it cooks or after it cooks, see where you end up. This can also like silverjirachi said be very gradual, one thing at a time. I make rice and eat it with butter. Eventually I make rice with chicken broth, and eat it with butter. I start adding canned chicken. I start adding poultry seasoning. I start adding dehydrated chopped onion. I start cutting up a little fresh onion. Sometimes I throw an egg in there now. I have a couple other rice cooker recipes of similar complexity. I still don't really use perishable ingredients except sometimes onion, because my executive function isn't that reliable.
Somehow never occurred to me I can use my rice cooker to cook things WITH the rice. So cool!!

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If you're comfortable accusing anyone of faking disability, you're not a real ally to disabled people
One time when I was a kid a group of girls and I had to treat another student for hypothermia by ourselves because she had so many invisible health issues that the adults we asked for help didn't believe us. The student in question was actively hallucinating. When I finally ran for help the people I grabbed were slow as shit to respond, casually joking about how "dramatic" the person in question was.
The kid was picked up by an ambulance 30 minutes later.
Now as an adult working in security I get SO MANY folks- upper-middle aged mostly- coming to me to 'rat out' people they think are faking it.
I was once sent into a bathroom because a client demanded that the "fucker won't get out, so go drag them out"- I was NEVER going to do that, so I did a wellness check instead. You know who it was? A person recently released from the hospital after a car accident. They had a hole in their skull and major hearing loss. They couldn't answer the owner because they couldn't HEAR the owner.
Another time about a homeless man who got around town by kicking the ground from his wheelchair. "You know he doesn't actually need that thing, his legs work fine, it's just for pity points"- Oh, so he's not paralyzed, his wheelchair is performative? Funny story Dale, I actually know that guy, he was backed over by a truck and has chronic pain from his shattered pelvis. But sure, let's make him stand up and walk everywhere so nobody feels too bad for him and tries to help him or something.
"She doesn't need that scooter, I've seen her get out of it."
"Look how fat he is, because he just rides around and refuses to get up."
"She doesn't really need that cane- she comes here without it all the time"
Sincerely, truly, from the bottom of my heart- as someone who isn't physically disabled but hears this shit all the time- fuck off
guys can we normalize wearing a mask at the very least if you’re sick and not coughing like you have tuberculosis once every 30 seconds in communal areas like can we pleaseeeee normalize that. cause there has been some genuinely unbelievable shit going on lately
since ppl are raising awareness about hearing loss, id like to add that tinnitus is not a karmic punishment for carelessness, and can be caused by several different overlapping things. do not moralize your health or u will die. message to myself, mostly.
that "I consent" "I consent" "I don't consent! (isn't there someone you forgot to ask?)" meme, but with me, any plan ever, and my chronic health issues
hey if you're not a mobility aid user, and you want a simple way to make public spaces more accessible to those of us who are, i have a tip for you:
push in your chairs when you get up from tables.
when people don't push in their chairs, people with bulky aids like wheelchairs and rollators can't get through. also a lot of people who use canes have wider gaits than able bodied people, and having a chair in the middle of their walking path is a real obstruction. while some of us are able to push chairs out of our way, a lot of us are not, and wind up boxed in/out because somebody didn't push in their chair.
so if you want to do something simple that can make a big difference in terms of like. navigating an outdoor food court or a cafe or what have you. push in your chairs.

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chronic pain diagnoses are all like yeah we don't know what this is or why it happens. we also don't know how to treat it. good luck out there soldier
reminder that adhd medication isn’t a luxury or preference, but a lifesaving medication. a 10 year long study in the usa showed that, when properly medicated, the rate of car crashes people with adhd get into goes down significantly–men’s rate drops by 38%, and women’s by 42%. the med shortage, denial of meds by doctors, rising prices, and war on drugs has killed–with such a car dependent society, not driving frequently isn’t an option, which means we need better healthcare and need it now.
https://shorturl.at/8VD8B
edit because i forgot to explain: short link is to an article by the washington post, it should be free to read
I’m pretty sure there’s also been a study that unmedicated ADHD increases the risk of developing dementia in old age. I’ll get back to yall when I find the study
Found it and here’s a Washington Post article if you don’t want to read a medical journal.
@icy-moons thank you for this incredibly important addition!!! People with adhd are almost 3 times as likely to get dementia, and the way to prevent that is stimulant medication–more people need to know this
Not to mention being properly treated and medicated for ADHD reduces the likelihood of developing an addiction or substance use disorder.
The articles below are free to access, they cite their sources if you wanna check out the studies themselves.
ADHD medication is not a gateway drug. In fact, teens and adults who seek treatment for their ADHD symptoms are much less likely to abuse dr
To reduce the risk of substance-use disorders, treatment with stimulant medication should begin prior to 9 years of age, according to resear
ADD-certified therapist here. These claims are ALL TRUE. I don’t have the link to hand but properly medicating ADHD also reduces anxiety and depression rates and I’ve seen it improve eating and sleep over the long haul, and improve aggression in young children.
i just have this persistent feeling of “i’m not doing enough” combined with “i don’t have the energy to do anything” and it just really fucking sucks
oh you want to kill yourself? how about we send you to torture prison against your will. that will surely make you feel better
got a good grade in physical therapy because i ordered a sex toy life is fun
anyways tmi/nsfw warning but since it helped me and my therapist hadnt considered the idea before im willing to bet a lot of others havent either so im gonna share:
if you have vaginismus and struggle with dilating regularly i highly recommend looking into wearable toys. theyre generally vibrators that hook onto your clothes or your person in some way, and they're intended to be worn long-term and in public which means you can safely+comfortably just put it in and go about your day without having to sit down and do the whole production of dilating on its own. theyre usually curved to follow your body and soft/flexible unlike the dilators which are straight and stiff, so theyre imo easier to get in and less uncomfortable to ambiently exist with, and the long term aspect gives your body more time to adjust to having something there. and frankly the vibrator part is helpful too, a big part of vaginismus therapy is teaching your body that sensations there arent actually painful like it thinks so introducing positive stimulus helps it relax, bc functionally it kind of is a type of massage lol. but yeah again i know this is oversharing and tmi but i also know this disorder majorly sucks to have and feel like you cant make progress on so if it helps anyone else then yeehaw
actually ive decided these tags are important enough to go in the post body
image id under cut bc it wouldnt fit in alt
alao i don't know enough about vaginoplasty to feel comfortable saying whether the first tip would be useful for that dilating too but its something to keep in mind at least, i cant see any reason why it wouldnt work the same though
i dislike "hey rb this actually" type things so if you dont want to thats completely fine esp considering a good chunk of it is abt vibrators lol, however it would be greatly appreciated as vaginismus was never mentioned in school / health class for me and ppl really do end up assuming (or being told by assholes) that the pain is just how it works and they have to push through it to be normal, i learned abt it somewhat early on bc mine was so severe i straight up thought i simply Didnt Have A Vaginal Canal and wanted to see if that was a thing, but for a lot of people its more subtle where penetration is /possible/ just not /comfortable/ so they think "ah this must just be how it works, everyone must experience this when they have sex so i just have to deal with it", which sucks on its own but is also something often taken advantage of/encouraged by abusive partners. or those with low/no libido* often find out when they reach the age for their first pap smear and either are in way more pain than normal for it, or are just straight up unable to complete it and then have to wait until after therapy finishes to get that test, so i want to give anyone i can a head start on that realization lol. and even medical stuff aside, the mental impact of not being able to engage in sex the "normal" way despite wanting to is really rough on its own, it's even been really rough for me and i'm transmasc so to a certain degree ive found it gender affirming not being able to do it """the girl way""", but at a certain point that just became a sprinkles-on-a-turd kind of thing yknow lol
*can also include those with active libidos who just choose not to sleep with anyone, but theyre a bit more likely to find out via masturbation whereas someone without probably won't feel the need to explore what's going on there as much
also i wanted to add vis a vis the physical therapy part, the "having a doctors finger in you" part does feel weird and awkward and embarassing and yes probably will hurt a bit when youre first starting out, but they will go as slow as you need and it really is helpful, because from that they can tell you what areas to focus pressure on with the dilator, test muscle control, make sure youre doing kegels/breathing exercises right, and gauge your progress while making sure youre not pushing too fast, so if youre willing/able to push thru the awkwardness of it then it really is worth it
editing bc i think this has started showing up on ppls fyps: there's another version of this post here where i go into more detail about treatment options, including a breakdown of the instructions my therapist gave me for mine, so if this post helped out then i would check out that version too! đź’•

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Fun fact: if someone tells you that they've got misophonia and that they can't stand a specific sound, and you start making that sound on purpose and won't stop doing it before they forcibly physically stop you from doing it, you were the one who escalated the situation to violence.
psa
no one fucking tells you this so here it is:
when signing out forms to apply for disability / filling out a form for diagnosis
you’re supposed to fill it out as you on your worst days
like, I filled out forms that said I could do most things usually
like, my doctor added in the conditions like “yeah, they can feed themselves when not stressed” “they can do this when not stressed”
but how I should have filled it out was more like
“some days I can’t feed myself” “some days I can’t leave the house”
My doctor didn’t even know this, but I talked to someone who had worked with people with both developmental and intellectual disabilities for a number of years, and she told me to write down how it is for your bad days
this should be a thing they tell you, but it isn’t
part of the reason I didn’t get my autism diagnosis as soon as I should have is because I filled out forms wrong!
This also goes for filling out forms for disabled parking rights. I’ve been rejected multiple times for a pass cause I didn’t find this out till recently.
Also you’re generally supposed to fill it out as you are without help.
That throws me too. Because the more help I get, the more capable I get. It’s easy to forget what happens when the help falls away even partially let alone completely.