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No way I was ever a competitive gymnast

Anyone else sometimes forget the level of disabled they are because it's so normal to yourself?

Sometimes i'll remember something i used to do, something i was able to do and that i definitely wasn't thinking about and i'll have trouble believing it. I know i was walking up and down stairs multiple times a day everyday and oftentimes running them but. It just doesn't true. Like, what do you mean i used to walk a kilometre to school and back every day when i was only half my size?? That can't possibly be right? But somehow it is! I used to jump on those garden trampolines for hours on end. How???

The sarcasm here is fucking hilarious 💀 whenever I inevitably end up using mobility aids, imma just tell them my doctor told me to, bcs she did. Even if your doctor denies you a mobility aid, people get uncomfortable if you just say a doctor made you, so you could always just make stuff up.

You shouldn't get a wheelchair, walker, cane, shower chair, or any kind of assistive technology mobility aid because then you might become dependent on them. Just like how you also shouldn't get glasses if you have bad eyesight because then you might become dependent on those.

For instance, if you end up stuck using corrective eyewear, you could actually lose your ability to tell what things are even when they are extremely blurry! You need to get used to having migraines from seeing unclearly because if you wear glasses all the time, you are basically giving up!! You don't need to see things coming at you from far away! You just need to get good at dodging, and if you can't, then you have no one to blame but yourself!!

For example, I read a really heart-worming article recently about a girl who was stuck using glasses - just absolutely, tragically trapped in her eyewear from dawn to dusk, even though she was good and never ever complained; and I heard she trained herself to discern the blurry faces of her loved ones with 60% accuracy! - she was even able to walk down the aisle at her wedding WITHOUT forcing the discomfort of seeing a woman in glasses on all her guests!!

Sure, she had to give her vows with a splitting headache, and she couldn't see her husband's expression when he said "I do," but overall, SO inspi-ration-al!!! So up-lifting!!

(She didn't even have to use a seeing eye cane, which would have been the worst-case scenario, obviously, because she worked hard to make sure she looked LESS disabled, not MORE disabled!!! Everyone knows blind people exist solely to be a cautionary tale to sighted people!!)

Also, did you know some people get glasses when they only need them a little bit?? How selfish of them! Sure, there's not a shortage, and an increase in demand would result in overall increased accessibility to glasses--but emotionally it's like taking glasses away from someone who needs them more! After all, if everyone who needed glasses got them, then...... um...... more people would have glasses! Which is probably bad!!!!

I also had a friend who was trapped in glasses who saved up all her money for laser eye surgery, and I don't know why everyone doesn't just do that! Sure, some doctors say some people don't "qualify" and it "won't help" those people, but that's why you can't give up!! You don't want to be one of those people!

After all, what's the worse thing that could happen with an unnecessary laser surgery to the face that comes with crippling debt??? It's worth the risk to gain your FREEDOM back, and I'm so proud of my friend!!

Tragically, she did die later that year while driving Uber and squinting at street signs, but at least now I know my friend is finally free from the shackles of her terrible eyesight. #ripAshley #rippedAshley #justripit 😌😌😌❤😇😇😇

And that's why you shouldn't get used to using a mobility aid!! Because, like glasses, they are inherently embarrassing to be seen with; and - like glasses - it is more noble to silently suffer than to depend on unnatural technologies that force you to rely on them!!! (Besides, everyone else will be SO much more comfortable if you look normal!)

I hope you learned something today. 💖

current least favorite thing about my latest chronic illness flare up is how boring it is like I'm stuck lying down in bed and my brain won't let me do anything

like I was going okay I can't go into uni but I guess I can write my papers but nope not an option so then I was like well I can write fic but no also can't do that so then I was like okay let's watch the eras tour movie and I only got half way through that!!!

the point here is I'm bored and have most of the next chapter of my Tess lives story written but it's all disconnected scenes that I need to join up and I want it done and it's not :(

For those out their with heds that use mobility devices, what device do you use and what was the point that made it a need ? I’m so tired and I’m pain on the daily in either my hips, knees or ankles (and that’s only below the waist)

I’m dependent on my parents for getting care and they are relatively supportive as disability is common in our family but my mom seems reluctant to even discuss the possibility that I may need an aid.

Any advice?

(Also going to the doctor this week to ask about symptoms of pots I’ve been having for years and stomach problems)

Just Eddie😍

im not a doctor, im just also a mess of shitty cartilage, and this is my experience, so like, dont quote me or anything lol

neoprene knee braces and ankle brace work pretty well, but i can never sleep in them, its just very uncomfortable, it gets really sweaty and kind sore. ive not yet tried elbow/shoulder/wrist braces, but i imagine its a similar experience. they do limit joint movement to an extent, but that means it can also be hard to go about your business. i think id recommend full on braces for liek, exercising, and particularly wobbly days. on better days, flex tape works pretty well

hope this helps!

dumb question but do those joint braces keep your joints in place and could i use them for subluxations