#illness/injury

[in-my-nunnery]

Oh my, did we actually get a literal whumpy, sickficky hurt/comfort scenario served on a platter there with poor SrF coming off her bike in the snow?

The fic ideas are flowing 😮‍💨

[chaoticautie]

As someone who is somewhat of a “veteran” of the online ND community, I’m disappointed in the lack of positivity and love for lesser known diverse cognitive conditions, and the opposing abundance of posts about “cures” or outdated criteria or treatments for those conditions. So, without further ado, I want to say hello to anyone with any of the disorders I’m listing, and give them the love and support that hardly anyone else in our community has… Shoutout to:

People with Down syndrome

People with Fragile X

People with William’s syndrome

People with dyslexia

People with dyspraxia

People with dyscalculia

People with dysgraphia

People with Prader-Willi syndrome

People with PANS or PANDAS

People with aphasia

People with a TBI (traumatic brain injury)

People with chronic/early onset mental illnesses

People with cerebral palsy

People with FASD or were otherwise disabled via other substances in utero

And many, many more I may have forgotten to list (but still support and love, I will add more to my list)

You are all beautiful and wonderful, and you all deserve so more love, appreciation, acceptance and support. You are just as neurodiverse as the rest of us, and your voices deserve to be heard and amplified.

I love you all ❤️

[hinamie]

domain expansion

[positivelyqueer]

give love to people with traumatic brain injury, acquired brain injury, stroke, neurological condition, worsening mental health, trauma, PTSD and all other brain based conditions that make you feel conflicted about your identity. About whether or not you’re the ‘same person’ you were before your injury or illness. People constant evolve and change but can be more difficult when changes more sudden, pronounced, and noticed by others. I hope you are doing well and are able to find some peace, support and love.

[chestnutroan]

waking up

[potato-lord-but-not]

get shown affection IDIOT

[vintage-fuzz]

Thinking about the possibility of Fiddleford noticing various random injuries & unexplained bruises that Ford would’ve received from when he was possessed.

Thinking about how he’d be concerned for his friend, only for Ford to shut him out, not wanting to reveal the existence of his “muse”.

Thinking about, despite his best efforts, Fiddleford would be forced to watch Ford suffer in silence, unwilling to tell him the truth.

[hedgehog-moss]

Help me settle a debate with my friends! If it seems difficult to choose that's normal, we've already dealt with the animals that are easy to sort (e.g. goats and mice are the two extremes on the spectrum of animal civility) and these are the more dicey choices that are on a similar level of perceived politeness.

[spinzolliii]

People forget that recovering from an injury takes so much energy. It’s not just pain, but a constant exhaustion as your body dedicates all of its resources to repairing itself. This can last weeks or months.

The same is true in the aftermath of a severe illness. You’re not necessarily “well” after the infection passes. Your body has to recover from the damage done by the infection. It leaves a person weak and lethargic well after they’ve “recovered” from their illness.

So, imagine a Whumpee being forced to work again immediately after an illness or injury.

[4axel4loop]

The Next One / Antigonick, Anne Carson

[nebulow]

It almost seems like non-disabled people have a harder time accepting when a chronically disabled person will never get better - and maybe even deteriorate over time, than the affected person has.

"Aww don't lose hope"

There is no hope to be had? Stop pushing your toxic positivity down my throat when I have come to terms with my situation and am grieving already.

Losing hope is what has given me an ounce of peace of mind. This is what life is now. It's not your grief, it's mine.

[noagskryf]

"i wish i could unmask wherever i went." "i wish i was visibly disabled."

Okay, fine.

Do you also wish you were pulled out of class and asked if you've taken illegal substances because you weren't masking?

Do you wish you were just not allowed in class sometimes because of your symptoms being disruptive?

Do you wish parents would pull their children away from you because you walk funny and make weird noises?

Do you wish your parents got sympathy glances whenever youre out in public with them?

Do you wish all this? Or do you wish you were more accepted by society?

EDIT: i think im not very good at explaining myself, this post is targeted at people who say "i wish i was visibly disabled" and then go on to deny that visibly disabled people experience a lot of ableism and danger because of it. this isn't targeted at people who wish they didnt have to hide themselves.

[worms-in-my-brain]

Grabbing you by the ears. Disabled people do not have to explain ourselves to other people. If I can’t do it, that’s all the information you need! You’re not entitled to my life or medical information!

[ieatratsforbreakfast]

I feel like most able bodied people see wheelchairs as the worst thing that could happen to a person. When I discuss my want to have a wheelchair for various reasons, most peoples first reaction is to be surprised that I could voluntarily consider that.

But what they fail to consider is that, unlike them, I very much hate walking. It causes me pain and fatigue, it is a miserable experience.

So to any able bodied person reading this, yes some wheelchair users like walking, some want to gain that ability back, but that does not invalidate the feelings of wheelchair users who absolutely hate walking.

[whump-side]

Whumptober 2024

No. 1: RACE AGAINST THE CLOCK

Search Party

[stellaltumi]

shoutout to all the fellow disabled people who spread awareness and advocacy even when they have no energy to do so, I see you, I love you, and you are so deeply appreciated. your story has the potential to be someone else's survival guide.