I feel like we don’t talk enough about how having chronic illness and/or chronic pain makes you irritable. It makes you grumpy. It can make you a not very fun person to be around.
We don’t talk enough about the ugly sides of chronic illness/pain. The parts where you feel like a bad person not because of the pain in of itself but because everyone else thinks you are pushing them away. The times when you don’t bear it like a saint and the roughest edges of your personality come out. Where maybe you do hurt other people’s feelings. Its a complicated side of the experience thats resists an easy answer.
i dont think the r slur needs to be reclaimed actually i think we can just leave that one where it is. it makes it very easy to identify what kind of person someone is when they use it
another mental illness meme i made out of boredom
Basic Respect for Cane Users
[IMAGE DESCRIPTION]
Pic 1: A title card that says ‘basic respect for cane users’.
Pic 2: Not all cane users are: physically weak, slow, elderly. Some cane users can: run, lift heavy things, ride bikes, skateboards, etc. Cane users are not all the same.
Pic 3: Do: move out of the way for someone using a cane, give your seat to a cane user on public transport, offer to carry something for your friend or co worker with a cane, ask cane users what their access needs are, treat cane users with respect. Remember that not everyone with a physical disability uses a mobility aid.
Pic 4: DON’T: touch cane users without their explicit permission, make assumptions about whether someone 'really’ needs their cane, give unwanted advice about someones disability, make a cane user feel bad or like they’re an embarassment. Remember: people might not use their cane full-time, you can’t know if someone is faking.
This is a question blind people get almost every time they go online, use phones, write, etc. Sometimes the questions are genuine and gently curious. More often than not they hold assumptions meant to mock, to silence, or even to justify harassment. Often, this is a way to accuse blind people of faking.
While there are bigger issues within the system, this kind of ableism perpetuated by individuals can be harmful and often makes the bigger issues worse or renders them invisible to the general public. For example, assumptions like the ones hidden in the question in the title are what keep blind people from employment. This kind of ableism can be used to justify physical violence.
While we may feel like we can’t fix systemic issues, the best things the average person can do is educate ourselves and change our behavior. This is true for ableism. If you ask the questions I list above, you are dealing with ableism.
Yes, even if that is not your intent.
To read more about how ableism harms blind people, check out this post about myths.
Here is this post where I answer your common questions.
Here is a post about making content accessible for blind people. You will find information there about how blind people use online, print, Braille, and audio content. Link here.
Here is a post about how people write in Braille.
You are online now. You should have access to a search engine. Put in some work. You can also search on YouTube if you like videos or audio.
I have a post for that as well.
First, do your own research. This will remove the assumptions from most questions you have. People are also more willing to answer questions they have not heard millions of times. Also, examine your reasons for asking. Do you want to know because you don’t want to look it up yourself or are you looking for ways you might best help your student or a co-worker?
Second, accept no as an answer. Note that some people are perfectly fine answering questions in person, but some are not. Also, online questions can get overwhelming and frustrating, mostly because people are able to research before asking and choose not to.
Most people are happy to answer questions from children.
Third, consider going to people open to doing the work. Pay them if possible. That includes people writing books, consulting, doing presentations, or even blogs like mine that are specifically dedicated to answering questions. The difference is that we are prepared to do this and can do so when we choose. You aren’t stopping us when we’re in the check-out line or on a date. At least I hope not.
Fourth, listen to what that person says.
If you engaged in this before, change your behavior. Inform your friends and family. Support blind people. You can do so financially by donating a nonprofit helping blind people such as the ones listed on my blog. You can also buy things from this list of businesses.
Pyromania info masterpost
Wip, prone to updates and accepting submissions
Pyromaniac characters(link)
Fire classifications(link)
List of things I did(link)
Symptom list(link)
Pyromania vs pyrophilia(link)
Possible causes(link)
Activities to cope(link)
Pyromaniobjectum(link)
Pyromania blogs(link)
@clusterrune @delightfulweepingwillows @hewasanamericangirl
i wish people knew what a developmental disability was, and I wish people didn’t think intellectual disability made you undeserving of respect.
i am developmentally disabled. i am not intellectually disabled. while I am semi independent, i still need some external assistance for my developmental disabilities. i keep investigating programs for housing, job assistance, etc. for “people with developmental disabilities” and not qualifying because I don’t have an intellectual disability.
yes there should be programs specifically for intellectually disabled people. but do your research on what a developmental disability is before offering us services.
and STOP saying “oh but you’re not INTELLECTUALLY disabled” “but you’re not one of THOSE disabled people.” Intellectually disabled people deserve respect.
hey i just wanted to give a shout out to people with personality disorders real quick. your disorder doesn't make you evil, it doesnt make you an abuser, and it doesnt make you unlovable. you're just as deserving of respect, care, and support as people without personality disorders. stay safe, i love you and i hope you have a happy holiday season. we're in this together <3
a way you can help some i/dd and cognitively disabled people is by clarifying what kind of response you want if you're not open to any kind of response
like, specifying that you want comfort or advice or solidarity or some other kind of acknowledgement, or if you want just an emoji or to change the subject, or if you want to close the conversation, like
just fucking communicate. give us feedback. tell us what you want
if you need clarification ask for it. if you need us to rephrase ask for it
we're communicating or verbalizing the only way we know how. and if you're not like this you can't even begin to scrape the fucking surface of understanding how hard it is
Do you have any advice for dealing with Kleptomania? I'm realizing I might be...uh...that, and it's one of those things people stigmatize to hell and back, but not one of those things I've seen or heard a lot about.
I'm not dumb enough to think it's just "uwu help I'm so quirky I stole stuff" disease and it's probably not like...completely uncontrollable, but I tend to experience worse symptoms when I'm stressed and feel out of control, so any advice would help a ton.
First of all, I am so sorry you deal with this as well. I absolutely understand how stressful and overwhelming it can be, especially when you're first realizing it.
My biggest piece of advice is try and find ways to reroute it..kinda like creating loopholes for it so that the urge to steal can still be satisfied in non dangerous ways (e.g ways that won't result in prison time or legal trouble)
This is how I've managed to cope with it and the symptoms have become much less stressful. My number 1 loopholes are:
Taking things that aren't owned by anyone and allowing my brain to view it as stealing. (Pennies on the ground, rocks outside of restaurants, free pens or candies from businesses etc.)
"Borrowing" things from my friends and partners, especially those who know about my kleptomania and make a big deal of pretending to really be concerned about what I've taken.
Advice that doesn't relate to actually giving in (somewhat) to the urges are:
Keeping my hands busy while in stores or other locations that trigger the impulses. I like to use subtle stim toys, but things like a phone can help too.
Wearing clothing that would make it super hard to steal (bright clothing, no pockets, very small bags etc) Knowing that I wouldn't be able to get away with it tends to keep me from giving in.
Listening to music or journaling helps with the anxiety that comes along with it.
I've only recently been actively working on this, but as I discover more things I'll share them here. And if you have any other questions, please feel free to ask!! I hope this helps 💜💜
Raven, he/him, 20, multiple disabled (see pinned for more details.) This is my disability advocacy blog
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