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! I will not allow homophobia, transphobia, racism, ableism, or any other discriminatory behavior here !

! I use any pronouns !

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hon3vbees

despite being diagnosed for 5 years now i still sometimes convince myself i made my tourettes up but then i hit a tic so completely absurd with no warning before it that theres genuinely no reasonable explanation for me doing it other than something fucked up happening in my brain

lupusbaby

Say it with me! Wheelchairs aren’t sad! Mobility aids aren’t sad! Mobility aids are instruments of freedom!

goth-princess-gwennie

Forgive me if this is inappropriate but

So are

colostomy bags

Diapers

insulin pumps

Oxygen systems

Braces

cuntpunkop-ed

catheters

rollators

hearing aids

compression garments

prosthetics

FREEDOM AIDS

seraph1c-mo0n

- canes

- service animals

- noise cancelling headphones/ear defenders

- wheelchair attachments

- fidgets

IT’S DISABILITY PRIDE MONTH YALL

BE UNAPOLOGETICALLY DISABLED AND TAKE UP ALL THE SPACE AND TIME YOU NEED!!!!!

tic-loud-tic-proud

Happy disability pride month y'all!

cowboyjoshdun

really love keeping up with my mutuals through their little tags and vent posts. getting updates on how they’re doing is something like: glad to know your job at the library is going well. i’m sorry you haven’t gotten that raise. glad your finals went well. i’m sorry your teacher is so unhelpful. glad your tv show got renewed. i’m sorry they killed your favorite character. glad that you scored tickets to see your favorite artist. i’m sorry they aren’t touring near you at all. glad your cat is doing well. i’m sorry your mom is sick again. glad you’re feeling better now that it’s your favorite season. i’m sorry your meds aren’t working. glad you’re married now. i’m sorry you have to step back for your mental health. glad you’re still here. i’m sorry life is so hard. glad you’re alive, i hope things get easier for you soon

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rubysapphrald

i feel so defensive and protective of people with ARFID like if i had a disorder that made my brain register 90% of food as poison for no reason and i had a bazillion people on the internet constantly calling me a manchild who needs to just grow up and stop being a picky eater i would start killing people

soracities

Mia Mingus, from "'Disability Justice' is Simply Another Term for Love", pub. Leavings [ID'd]

socialmasochist

Stop. Leaving. Disabled. People. Out. Of. Your. Activism.

(I know we’re extra scary because any of you could become disabled in a blink of an eye, but ignoring us won’t make that threat go away.)

prokopetz

Level 1: Asylums are scary because there's crazy people there.

Level 2: We shouldn't treat mental health facilities as objects of horror because it stigmatises mental illness.

Level 3: Asylums are scary because there's psychiatrists there.

frogsfordisabilityjustice

No, your event is not a 'safe space' for queer kids if disabled queer kids cannot access or attend it safely.

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disabled-bug

Idk what person with chronic illness needs to hear this, but you can do things to make your responsibilities nicer for yourself. You can get an ice cream after a blood draw. You can sit down for tv time after an injection. You can pick out the bandaids that have cartoon characters on them instead of the plain ones. Being an adult doesn’t stop you from benefiting from encouragement. Go for whatever fits with your routine/abilities/budget and makes life a little better. A spoonful of sugar helps the medicine go down etc etc

Hello guys!!! It's been a while and I've been pretty quiet on this blog, so I wanted to give an update on what's been going on.

PANS and Lyme disease haven't been bothering me too much these past few months! Which is AMAZING. I'm back on immunotherapy after insurance/money issues, so that's helped a lot. Getting my wheelchair was also a massive help in saving my knees and getting around without massive pain, so thank you all so much again <3

Unfortunately I can't say the same for my mental health. I've been navigating a CPTSD diagnosis for almost 2 years now, but I'm still learning about it every day and it's still very up and down. A lot of the time, I frankly don't have the mental energy to keep up with this blog. BUT!!! I've been seeing a new therapist that specializes in CPTSD and it's been helping a TON, so don't worry!! I feel like I'm getting back on track to being somewhat mentally stable lol.

I'm also still focusing more on political activism than chronic illness advocacy (though they do overlap quite a lot), so I've been using more energy there. That won't change until whatever the fuck is happening in the U.S. changes. Politics probably will be mentioned here often!

Anyway, long paragraphs aside, I'm still kicking :)

#thank you so much to everyone who's still here #ik I've been very on and off with this blog the past 2 years #life is fucking crazy #I'm still trying to figure out how to navigate it after everything changed so suddenly #but I still want to be here on this blog because I love the community #also... not to get sappy #but during the time i was consistent with this blog i was actively going through the trauma i'm now processing #i focused on chronic illness and didn't speak much about what i was going through #but for the people that've been here that long #you were a source of hope for me

lifeafterpsychiatry

It's always "stop harming yourself or we'll have to lock you up!!!" and never "what do you need to change to want to harm yourself less and how can we help you make some of these changes?" and that's why we're not getting anywhere

quinnbites

Posting a mutual aid request. I am severely disabled (suspected pots, maybe me/cfs or long covid, among other probabilities that need to be tested for/ruled out) and facing threats of homelessness. It is specifically because I am disabled/unable to work unfortunately, because my girlfriend has tried her best to cover our rent in it's entirety despite me being so sick. Shares/likes/comments heavily appreciated. I also have art commissions open if you'd prefer to do that (check pinned post). Please ignore my deadname, sigh.

My name is Aubrey Allen. I am 22 years old and the past two years I have… Aubrey Allen needs your support for Help Aubrey Find a Safe Home a

gentleaffirmations

Even if you were a difficult child, you didn't deserve to be hurt.

gentleaffirmations

I hope this message reaches all the neurodiverse and disabled people who were made to feel like their abuse was justified because they had "behaviors".

While this message is true for every child, you are who I had in mind when I wrote it.

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Anyone have any tips for dealing with nausea? I may have asked this question before, but I can't find it 😭

As a chronically ill emetophobic, I am NOT having a fun time

#already tried antacids #and sleeping in the bathroom #don't have immediate access to zofran #pressure point on the wrist kinda works but not enough #chronic illness #actually chronically ill #chronically ill

I have a tic that makes me scrape my heel against the floor when I walk, and sometimes it trips me up so I have to do a little hop to avoid tripping. I'm straight up galloping around my college campus rn </3

#chronic illness #actually chronically ill #chronically ill #tic disorder #pans syndrome

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