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Mobility Aid King

@boywithbear / boywithbear.tumblr.com

27, white, intersex, genderqueer trans man, homoflexible angled aroace, physically disabled & neurodivergent • no blog theme, I post everything on this blog (mostly queer and disabled related stuff and shitposts) • flag making is part of a special interest, tag on here is my flags and new flag acc is @whalien-flags • other random tags can be for personal reasons (fine to reblog); possible nsfw posts will be under nsft tag so minors dni • icon id is 8 stripe rainbow flag colored 7 petal agust d lotus flower and header id is a geometric 8 stripe rainbow flag.

yknow what am finally gonna make a pinned post

if you like bts + similar artists (including more alternative/indie Korean artists and some Chinese artists) and/or pride art in general stuff (esp fandom related) then check out my shops! 💜 I have MANY different things on my redbubble and etsy both designs and product options wise; I also have some of my flags I've made uploaded on my redbubble as pins and stickers! My etsy is mostly pride flag kandi/beadwork (+ rainbow loom now), bts kandi, and some print-on-demand stickers and pins! :] I have a lot of stuff that is bts/kpop related but also a lot that isn't! But almost everything is queer related. :D

I also do pride edits in general for bts and similar artists, so I’m just gonna link my entire linktree. :3 (my flag coining archive is linked there as well!)

Having a traumatic childhood means you cannot talk even objectively about your basic foundational experiences without it being "venting", even if you're not actually venting. You just straight up have a huge chunk of your life you can't talk about, full stop, without it being trauma dumping.

And it not being socially acceptable to talk about your own childhood is super alienating. Sometimes people want to know why, and any answer you can give them is going to be off putting.

It's to the point I get irritated when something I said is framed as venting when I'm literally just talking about my life experiences, doing my best to keep emotion out of it.

when I was in high school, I overheard two older students talking about a friend of theirs.

One of them said something like, "it doesn't bother me that [Friend] was in residential mental health treatment, I just wish they wouldn't talk about it ALL the time".

The other replied, "Well, that was all of last year for them. So when they say 'when I was in treatment,' it's like when you say 'last year'."

I try to remember that any time someone says something that sounds Shocking to me. sometimes one person's scary special crisis is another person's last year.

If you want to be accepting of mental illness, you need to accept the fact that some people's everyday lives are going to be terrifying to you. That doesn't mean they don't get to talk about it. Stop forcing hurt, isolated people to become even MORE hurt and isolated because you can't fathom toughening up a bit.

For disability pride, think I want to focus on this one thing that been bothering me

Been very frustrated lately by lack of phone call accessibility as someone who lacks speech but needs a lot of resources to stay healthy.

With rise of AI, it's only getting worse and worse.

More places changing their systems to incorporate AI answering machines.

Thing is...

Whenever I hear most people ranting about this change, it's usually about how annoying it is from an abled-person perspective or environmental or ethical impact.

Which are important valid reasons to be upset. I share those sentiments too.

But feel like disability is once again forgotten about within important discussion about change.

AI creates terrible language accessibility issues.

In fact, that's why it so annoying to deal with it.

In the past, if a place didn't have a call center or desk person to answer calls, they use extentions.

That meant you had to press a few numbers to get the right person.

Now with AI, you're expected to have a full conversation with a robot.

Tell them why you're calling, who you need to speak to, verify your info so the humans don't have to later, etc.

These bots can be bad at understanding what able-people are saying, so imagine how they handle these disabled callers:

  • People who use AAC (speech aids/devices)
  • People who slur, stutter, have "strange" voice or pronunciation
  • People with rapid or disorganized speech
  • People who use poor grammar & who don't speak full words or sentences
  • People who mix up similar common words
  • People with "deaf accent"

(i don't know if there is a different preferred term for this. Im sorry if I sound offensive. Please Lmk)

  • People with non-communicative speech such as vocal tics, echolalia, or babbling
  • Anyone who uses speech or language in a way that needs a human mind to interpret
  • Anyone whose voice sounds notably different

Ability to understand what AI is saying can be harder too:

  • d/Deaf people and other hearing differences
  • Auditory processing disorder
  • Receptive language disorder
  • Developmental disability, especially intellectual and learning disabilities

(AI can't help people who need things explained a certain way. AI unreliable and fails to adapt a lot.)

  • Anyone who frequently can't make out sounds and/or speech
  • Anyone who frequently has trouble with meanings in conversation

The problems I often face with AI answering machines (and that I'm sure many other disabled people have faced as well):

  • AI slightly mishearing me/my device
  • AI mishearing so badly that it basically makes up a fake conversation
  • AI not hearing me/my device at all
  • AI registering tics and stims as answers
  • AI "explaining" an instruction by repeating the same instruction again word-for-word
  • AI directing me to the wrong person without trying to confirm what I said
  • AI sometimes just... hanging up on me right after I speak my first answer...

These are the machines being put in front of

  • hospitals
  • doctors offices
  • mental health centers
  • pharmacies
  • transportation and in-home care
  • health insurance member services
  • medical supply companies
  • government resource agencies
  • non-profit organizations
  • advocacy groups
  • justice centers & other legal resources
  • customer service lines
  • many other places disabled people often need to access from home

It's another example of some of the most vulnerable being pushed away from the things we need, and we're also being forgotten in these discussions about things that can affect us a lot

Next time someone is ranting about AI job interviewers, please also remember:

  • the AI pharmacy assistants that make it impossible for someone with a speech disorder to sort out their meds
  • the AI scheduler that won't allow a D/deaf person to access the right extension of the clinic to set up an appointment
  • the AI agent that confuses an intellectually disabled person into anger and tears
  • the AI answerer that hangs up on a mentally ill person seeking help in crisis because they aren't speaking coherently enough

Human beings need to be at the forefront of human resources and issues for disabled people especially. Please remember us. Please fight.

Happy disability pride ♡

This post is so funny literally proving OOP’s point. Most of “transfeminist” Tumblr can’t handle how queer people described themselves in the 90’s either. Ntm that at least 50% of these are clearly transfems describing themselves, which it’s pretty fucking transmisogynistic to police the language they’re using. The only possible issue is the use of the h-word if said person wasn’t intersex but it’s the 90’s. All these people sound cool as fuck and would probably call OP a cop

Also this is "My Gender Workbook" by Kate Bornstein a transfem who literally helped to pave way for transfeminism (in fact this book is arguably the first ever transfeminist workbook) and these are the replies that she chose to include in her book about gender diversity.

It's very clear that for many people, the mere act of supporting a transgender man or transmasc person is enough to throw trans women and transfem people under the bus, even including transfem people who have spent decades developing transfeminism and gender activism.

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dawoudi

I am now on my fifth day without food… surviving only on water Not because I’m fasting by choice . I do this to save whatever little food I can for my family.

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dawoudi

The food we have left wouldn’t last a day if we all ate. So I stay hungry. I drink water to quiet the pain, to stay standing, to keep going. Every bite I don’t eat means one more bite for my kids.

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dawoudi

My body is getting weaker, but a parent’s love is stronger than hunger.

The famine is real. The suffering is deep.

Please don’t look away.

@dawoudi and I speak almost every day. Every day I ask him how he's doing and hope he can tell me he's been able to eat something. He tells me not to worry, but I can't help it, because my heart is breaking.

Please help him by donating to his family's fundraiser, so that they can buy food when it arrives on the market. Thank you. ❤️

It is #15 on the gazavetters list, and was also shared by @nabulsi here and here.

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drdarine

My father was at the market, as he always is, searching for anything that might ease our hunger. Under the relentless sun and on his seventh day without food, surviving only on water he collapsed from sheer exhaustion.

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drdarine

Thank God, he’s home now, beside me. But he’s terribly weak, as if his body can no longer carry the weight of life. I begged him to eat. I pleaded, just so he could stay with us a little longer. He hasn’t had chicken, or meat, or even fruit. God knows we don’t have those.

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drdarine

He finally took a few bites of dry bread. But watching him struggle to swallow, my throat tightened. The lump wasn’t just in his throat it was in my heart. Scraps of stale bread… which I begged him to eat, just so his heartbeat wouldn’t leave this home.

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drdarine

And in that moment, I understood.

I understood why he wasn’t eating.

Because sometimes, hunger "cruel as it is" is easier to bear than eating when your dignity is shattered. When you’re trapped, abandoned, and the world is watching in silence.

We at the @gazavetters team extend our heartfelt wishes for a swift recovery and complete safety to our brother AboAhmed @dawoudi and his honorable family.

We are all going through extremely difficult circumstances, and we pray that this hardship will soon pass, and that peace and security will prevail for everyone.

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drdarine

This is a historic event in every painful sense of the word a brutal war, massive destruction, and a famine devouring lives. Every moment of delay could mean the loss of another life.

What more can be said?

Stop the genocide. Lift the siege. Feed the hungry. Shelter the unhoused. Heal the hurt and ill.

End the occupation.

Free Palestine.

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dawoudi

I’m deeply thankful to be back home, surrounded by my children. Though my body is tired and frail, my heart still beats with strength, and my will remains unshaken.

These past days have been harsh, but it is dignity and patience that have truly kept me going. Hardship has not broken me and by God’s grace, it never will.

As long as there is breath in me "in all of us" we will stand tall, endure with courage, and keep praying for relief, not only for ourselves but for all who suffer.

You scared me. I'm glad you're ok. I know you're strong and you will keep going, but I still worry.

This cannot go on. This needs to end, so the people in Gaza can have peace, food, water, housing, and their health and dignity back.

Pressure your governments, share fundraisers, donate when you can.

Please.

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drdarine

What we’re enduring isn’t just hunger. It’s a daily assault on dignity. A test of patience.

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dawoudi

Your words truly touched me, reaching a place in my heart that only sincerity and love can reach.

Vetted! #15 on @/gazavetters vetted gfm list, promoted by @/gazavetters here, promoted by nabulsi (x, x, x, x).

In what world is it normal for a person to have to go for 7 days without food? Please, please, please support them in this incredibly difficult time!

You can get a postcard after you donate!

every year small towns and indigenous communities across canada are burnt to nothing by horrific wildfires and americans go on the internet to complain about it and blame us bc the smoke has spread to their state. i’m so tired.

go yell at mark carney or your own local politicians about climate change and urge them to do more to stop it. the namaygoosisagagun first nation had their community destroyed today. you can find a link to donate to them here. donate to your local food bank. go to the beach next week when the smoke clears and you don’t have to think about it anymore while the people who’s lives have been destroyed will have to pick up the pieces and try to move forward when we are already in a huge cost of living crisis across the country.

Hypothetical scenario: you're in public and you see someone using a walking cane (a cane for physical support/stability, not a white cane that blind people use). They're approaching a door that has an accessible push button to open it, and instead of pressing the button with their hand, they press it with the end of their cane.

What are your thoughts on using the bottom/end of a walking cane to press one of these buttons?

If you use a mobility aid but not a cane specifically, and this specific action would not be possible with your given mobility aid, choose the fitting non-cane answer.

Anon uses a cane and does this sometimes and no one ever says anything, but they worry that maybe it bothers people and they just don't say anything. Anon had never thought about it until recently when they saw someone hit the button with their shoe and anon got grossed out. They wonder if others view it the same way as using a shoe.

We ask your questions anonymously so you don’t have to! Submissions are open on the 1st and 15th of the month.

Cane and wheelchair user. DON'T DO THIS.

It's like using your shoe to open the door, who knows what germs you picked up while walking around. These buttons are typically higher up for wheelchair users and we need to use our hands to reach. These buttons also tend to break pretty easily from too much pressure or someone pushing against the door while the button has been pressed.

Also, when you use your cane to point or press buttons you aren't being properly supported and you will fall eventually.

Anon, it's okay you didn't know. But going forward please use your elbow ❤️

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Reblogged
When 18-year-old Roberto first experienced menstruation, she was terrified. Born intersex and raised as a boy, she had never been taught about periods, let alone how to manage one. Before that terrifying day, Roberto had spent her entire life in a quiet village in Kisii County. Her parents never disclosed anything about her intersex identity, partly because they did not fully understand it themselves, and partly due to the stigma surrounding differences in sex development. Roberto grew up playing football with boys, dressing like them, and following all the expectations of male childhood. Yet, as she entered adolescence, she began noticing subtle changes in her body that did not match those of her peers. She occasionally experienced discomfort, mood shifts, and physical traits she could not explain. With no information about intersex bodies or reproductive health, she simply brushed these feelings aside. Conversations about menstruation were reserved for girls, leaving Roberto completely unprepared for what was coming. “I thought I was bleeding to death, but I could not tell anyone, not even my mother,” she recalls. “I used an old T-shirt and hid it under my mattress.” It was only years later, after meeting a community health volunteer who worked with intersex and gender-diverse youth, that Roberto finally shared her experience. The volunteer explained what it meant to be intersex, helped her understand her body, and connected her to a safe support group. Through these conversations, Roberto slowly began embracing an identity that felt more aligned with who she truly was. She chose to use she/her pronouns because it was the first time she felt seen, understood, and comfortable in her own skin. “It felt like breathing freely for the first time,” she says. “Like I could finally be myself without fear.”

The hidden reality of intersex menstruators

Roberto’s experience reveals a little-known truth: intersex individuals who menstruate are often invisible in menstrual health policies, education, and aid programmes. While Kenya, and Africa more broadly, has made progress in addressing period poverty among girls and women, intersex people are left behind, navigating their cycles in silence and shame. When 23-year-old John first experienced menstruation, it was not a typical “coming-of-age” moment. Instead, it became a confusing and isolating chapter defined by stigma and secrecy. Growing up in South Nyanza, John lived in a household and a wider community that neither understood nor accepted their identity, let alone their menstrual health needs. “I bled in silence for years, and yet I could not talk to anyone,” they recount. “My mother kept asking why I was not ‘normal’, but I was too scared to explain something I did not even fully understand myself.” Intersex persons like Roberto and John are often excluded from the conversation about menstruation. “This is despite the fact that they suffer in silence,” says Margret Mogaka, a reproductive health advocate at the Kisii Teaching and Referral Hospital (KTRH). Although the Kenyan government launched the Menstrual Hygiene Management Policy in 2019 to promote menstrual equity, intersex individuals are not included. “Menstruation is still framed as a female-only issue,” says Mogaka. “This excludes not only trans men but also intersex people, many of whom menstruate and need the same support.” She adds that many public schools, clinics, and community programmes assume only girls need menstrual products or information. “This makes it nearly impossible for intersex menstruators to access sanitary pads or counseling without facing ridicule.” [...]

This is what I think about every single time I see people talking about period poverty, or helping women in places like Palestine access menstrual products.

It's obviously extremely important. But how often do those resources actually teach intersex and trans people who menstruate and aren't living as women? We likely can't even say because no one ever thinks about it.

As with so many issues caused by misogyny, all feminists can agree it's an extremely important issue UNTIL trans and intersex people point out their exclusion. And then suddenly people being unable to work or go to school because they are bleeding all over themselves isn't actually an issue, even though if you are living as a man it is then even MORE of an issue because it's not a problem you are "meant" to have.

Transmasc, nonbinary, and intersex inclusion in feminism, reproductive and menstrual activism, must not optional.

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cripplemetal

notes for my impostor syndrome:

• no, it's not painful to walk for abled-bodied people

• no, healthy people don't usually use every chance they get to lean against walls or sit down

• no, ableds don't dream about shower stool

• no, ableds don't celebrate days when they're not in pain. because usually they're not in pain

• no, ableds don't want to stop walking mid-way, lay down on the ground, curl up and cry and whine from pain

• no, ableds aren't exhausted by their own bodies 24/7

Hey man thanks for this I really needed it

found this today

Please use these terms correctly. Not doing so will deeply harm the people who actually have experienced trauma, gaslighting, triggers, and people who have NPD.

This needs to be shared wide and far. I’m so sick of people misusing these terms. Especially to draw and false sympathy to themselves.

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genderqueerdykes
Anonymous asked:

genuine question: what do tma and tme mean and why are they intersexist? i've seen them around but i don't know what they stand for

(again, genuine question, trying to learn)

good question!

they stand for "transmisogyny affected" and "transmisogyny exempt". the reason this is intersexist and transphobic in general is because more than trans women are affected by transmisogyny. a lot of trans men on T are confused for trans women and become targets of transmisogyny. femme gay men are affected by it. many cis women are affected by it, too, as rad fems love to try to "transvestigate", which just means misgendering women who don't match their idea of what a woman looks like

people literally use tme to mean afab and tma to mean amab. it's just the same shit all over again. its a needless binary that shouldn't exist. trans and intersex experiences are too broad for that

i hope that helps!

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Reblogged

actually I love using my disability as a crutch and an excuse and I think all disabled people should be allowed to do it as much as we want

"you guys are brainwashed idiots if being on rednote is what woke you up to chinese people being actual humans" might be swinging at a hornet's nest here but firstly, better late than never, secondly, we are aware that chinese people are learning the same about americans too, yes? there are fully grown adults on rednote who thought homeless americans were homeless on purpose because they're lazy and didn't learn the truth of it until americans told them otherwise. it does go both ways here. don't wish for change and then turn around shitting on the people who are changing

I've been disabled for almost 29 years. Here's what I've learned.

  • Tablets sink and capsules float. Separate out your tablets and capsules when you go to take them. Tip your head down when taking capsules and up when taking tablets. Liquigels don't matter, they kinda stay in the middle of whatever liquid is in your mouth.
  • If your pill tastes bad, coat it with a bit of butter or margarine. I learned this from my mom, who learned it from a pharmacist.
  • Being in pain every day isn't normal. Average people experience pain during exceptional moments, like when they stub their toe or jam their finger in a door, not when they sit cross-legged.
  • Make a medical binder. Make multiple medical binders. I have a small one that comes with me to appointments and two big ones that stay at home, one with old stuff and one with more recent stuff.
  • Find your icons. Some of mine include Daya Betty (drag queen with diabetes), Stef Sanjati (influencer with Waardenburg syndrome and ADHD), and Hank Green (guy with ulcerative colitis who... does a bunch of stuff). They don't have to be disabled in the same way as you. They don't even have to be real people. Put their pictures up somewhere if you want; I've been meaning to decorate my medical binders with pictures of my icons.
  • Take a bin, box, bag, basket, whatever and fill it with items to cope with. This can be stuff for mentally coping like colouring books or play clay or stuff for physically coping like pain medicine or physio tape.
  • Decorate your shit! My cane for at home has a plushie backpack clip hanging from the end of the handle and my cane for going places is covered in stickers. All of my medical binders have fun scrapbooking paper on the outside. Sometimes, I put stickers and washi tape on my inhalers and pill bottles. I used my Cricut to decorate my coping bin with quotes from my icons, like "I've seen enough of Ba Sing Se" and "I need you to be angrier with that bell".
  • If a flare-up is making you unable to eat or keep food down, consider going to the ER. A pharmacist once told me that since my eye flares can make me so nauseous that I cannot eat, then I need to go to the hospital when that happens.
  • Cola works wonders for nausea. I have mini cans of Diet Pepsi in my coping bin.
  • Shortbread is one of the only things I can eat when nauseous. Giant Tiger sells individually-wrapped servings of shortbread around Christmas or the British import store sells them year-round. I also keep these in my coping bin.
  • Unless it violates a pain contract or something, don't be afraid to go behind your doctor's back to get something they are refusing you. I got my cardiologist referral by getting in with a different NP at my primary care clinic than who I usually saw. I switched from Seroquel to Abilify by visiting a walk-in.
  • If you have a condition affecting your abdomen in some way (GI issues, reproductive problems, y'know) then invest in track pants that are too big. I bought some for my laparoscopy over a year ago and they've been handy for pelvic pain days, too. I've also heard loose pants are good for after colonoscopies.
  • Do whatever works, even if it's weird. I've sat on the floor of the Eaton Centre to take my pills. I've shoved heating pads down my front waistband to reach my uterus.
  • High-top Converse are good for weak ankles. I almost exclusively wear them.
  • You can reuse your pill bottles for stuff. I use my jumbo ones to store makeup sponges and my long skinny ones to hold a travel-size amount of Q-Tips.
  • Just because your diagnostics come back with nothing, it doesn't mean nothing is wrong. Maybe you were checking the wrong thing, or the diagnostic tool wasn't sensitive enough. I have bradycardia episodes even though multiple cardiac tests caught nothing. I probably have endometriosis even though my gynecologist didn't see anything.
  • You can bring your comfort item to appointments, and it's generally a green flag when someone talks to you about it. I brought a Squishmallow turkey (named Ulana) to my laparoscopy and they had her wearing my mask when I woke up. I brought a Build-A-Bear cat (named Blinx) to another procedure and a nurse told me that everyone in the hall on the way to the procedure room saw him and were talking about how cute he was. Both of those ended up being positive experiences and every person who talked to me about my plushies was nice to me. If you don't feel comfortable having it visible to your provider during the appointment, you can hide it in your bag and just know it's there, or if you're in a video appointment, you can hold it below frame in your lap.
  • Get a small bucket, fill it with stuff, and stick it in your bed (if you have room for it). I filled a bucket with Ensure, juice boxes, oatmeal bars, lotion, my rescue inhaler, etc. in October 2023 in anticipation of my laparoscopy and I still have it in my bed as of January 2025.
  • If your disability impacts your impulse control (e.g. ADHD, bipolar disorder), you should consider setting limits around your spending -- no more than X dollars at a time, nothing online unless it's absolutely necessary, and so on. Or, run these purchases by someone you trust before committing to them; I use my BFF groupchat to help talk sense into myself when I buy stuff.

Feel free to add on what you've learned about disability!