You're not lazy. You're overwhelmed.
taylor price
Xuebing Du

titsay

#extradirty
RMH

gracie abrams

No title available
Game of Thrones Daily
PUT YOUR BEARD IN MY MOUTH
trying on a metaphor
Jules of Nature
cherry valley forever
d e v o n
No title available
will byers stan first human second
One Nice Bug Per Day
Aqua Utopia|海の底で記憶を紡ぐ

bliss lane
almost home
EXPECTATIONS

seen from Türkiye

seen from Malaysia

seen from United Kingdom

seen from Netherlands

seen from United States
seen from United States

seen from Indonesia

seen from United States

seen from Türkiye

seen from Malaysia

seen from United States
seen from Bulgaria
seen from Malaysia

seen from United Kingdom
seen from Bangladesh
seen from United States

seen from Türkiye
seen from United States
seen from United States

seen from Türkiye
@adhd-informative
You're not lazy. You're overwhelmed.
abelds have this funky ability where they hear disabled people say they "can't" do something and instead of hearing "can't" as in, cannot, they hear "i can if i push myself and i just don't wanna". which is really interesting!
Disabled and chronically ill people are allowed to enjoy things and do things they like (if they’re able) while still being sick and disabled. Yes, even if they aren’t employed. Hope this helps.
Disability Pride shout out to everyone whose disability…
gets in the way of their sex life
gets in the way of expressing and/or understanding their sexuality
gets in the way of their romantic life
gets in the way of intimate relationships
gets in the way of exploring any/all of the above
something that might be hard to grasp is that. physically disabled people can do everything "right", follow all the recommended programs from doctors and medical practitioners and lose weight and do this exercise and that diet and this and that and they still can stay disabled. they still can get worse.
and it's imperative to understand that. doing things this way can be soul crushing. it's difficult, if not impossible for some people. and many people will not be able to do things "right" and will stay disabled or get worse. some people might, accidentally or on purpose, make their disability worse themselves. and those people don't deserve to be disabled any more than people who you think doesn't.
we cannot, cannot assign a moral value to disability. disability isn't a punishment for doing right or wrong. it is not a judgement. there is no moral value associated with being disabled.
people you find wonderful will be disabled. people who you think suck will be physically disabled. people who had no pre-existing condition, who did everything "right" and were healthy before will be disabled. people who had absolutely no means to change their lifestyle, because of poverty or location or some systematic issue, will be disabled. and people will be disabled as a direct result of their choices.
none of that, absolutely none of it, is an indication of whether that person "deserves" to be disabled or not. none of it is a reflection of their moral character. disability is simply a neutral fact of life.
A thing about how *I* experience chronic pain: it’s not always easy to quantify when I’m in “routine” pain, esp when it’s dull rather than sharp, but it absolutely *does* affect my functioning.
So much stuff about chronic pain, especially relating to pain scales, talks about relatively lower-level routine pain that “you no longer (actively) notice” as if it then becomes a zero sum game; you no longer notice it, therefore it no longer affects you?
But a lot of the pain I live with daily *is* dull rather than sharp. And quite a lot of it I’ve been living with various kinds of intermittently for most of my life. For example, digestive pain and nausea, dull headache, and ongoing musculoskeletal pain *definitely* do affect me even when I’m not actively noticing it. It eats spoons to do things. It makes me actively *considerably* more fatigued and actively reduces my emotional capacity to process rather than react. It also reduces my executive function *enormously*, and that is *not* great at the best of times.
The best analogy I can give is that it’s like background programmes running on a computer, eating processing power.
That moment when you have no one to listen to your info dump so you just walk around your room in circles ranting to yourself
sorry for being intense about everything, it’ll happen again
unfortunately a lot of the corny self help advice turns out to be true but the thing is you have to come to those conclusions yourself otherwise it just sounds dismissive and dumb
reblog to give prev a fUCKING BREAK in 2026
they should invent a taking care of your own body thats easy
I’m big on supporting others cause life aint easy
My PMDD isn’t that bad. I should be working, I say to myself while actively crying with tears streaming down my face.