Me when the illness is making me feel ill and the chronic pain is chronic and painful and the disability is disabling me and the fatigue is making me feel fatigued: 🥲
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@melodymorningdew
Me when the illness is making me feel ill and the chronic pain is chronic and painful and the disability is disabling me and the fatigue is making me feel fatigued: 🥲
reminder: just because a disabled person has accommodations does not mean they will perform at the same level or have the same capabilities as a non-disabled person! accommodations are there to make life easier for the disabled person, but they don’t erase the fact that we are disabled. as an employer, parent, peer, etc. you must be open to the possibility that a disabled person will be DISABLED by their condition. if you only see accommodations as an excuse to expect the same from a disabled person as you would from a non-disabled person, you are not the ally you think you are
Ahhh yes time to play my silly little game of "Is it burnout or depression or just plain ol' exhaustion?"
Finally I'm all moved and loving all the space I have in my room now!!! It's pretty sweet ^^ my bed net won't attach tho and it's making me sads. I want my princess curtain TwT
A word that ruined your life
I'll go first.
Limerence
Me when I haven't showered in over a week
Stop using me as a step ladder to feel better about yourself.
Follow your dreams, I guess
Pokemon Heritage Post
*Alternate words for disabled:
✨𝒫𝒶𝓈𝓈ℯ𝓃𝑔ℯ𝓇 𝓅𝓇𝒾𝓃𝒸ℯ𝓈𝓈✨
Sugar baby
Royalty (obvi the throne/the scepter)
Creature of the abyss (this is for my fellow hermits)
You may call me Your Majesty and I will accept nothing less
*this is a meme and not to be taken seriously pls do not call random disabled ppl sugar baby or creature or princess (I do not take responsibility for any consequences you may receive for doing this)
⚠️ Trigger warning for mentions of involuntary self harm ⚠️
The reality of being disabled and autistic is being covered in bruises bc you had a meltdown over last minute laundry and hit and bit yourself a bajillion times.
the incredible harsh quiet revelation that you have when you are diagnosed with chronic illness(es) is that you will never be healthy again. I don't think able bodied people are able to understand what it means to just resign to the fact that your life is not just yours anymore. you share it with a weight that will be with you until you are gone from this world.
As a wheelchair user I'm trying to reframe my language for "being in the way."
"I'm in the way," "I can't fit," and "I can't go there," is becoming "there's not enough space," "the walkway is too narrow," and "that place isn't accessible."
It's a small change, but to me it feels as if I'm redirecting blame from myself to the people that made these places inaccessible in the first place. I don't want people to just think that they're helping me, I want them to think that they're making up for someone else's wrongdoing. I want them to remember every time I've needed help as something someone else caused.
To the people saying this also applies to fat people - you are not derailing! This is true!!!
Comprehension is paramount.
“surely this will not cause my chronic illness to flare up,” i say, actively doing something that has never failed to flare my chronic illness
I annoy my GP bc I always have new problems :3
Why are physically abled people so stuck on getting off of or out of mobility aids????