Hate my guts

2018 ulcerative colitis.
2019 fibromyalgia.

Chronic illness is bullshit so let's all complain together 🌟(please stop hitting on me, I'm not here for that)🌟

[Hate my guts @IBDcanSmyD]

100%. I don't need more health issues, & it's likely that COVID would fuck me up

I want to live

I want to go back to pre-2020

I miss my friends

But none of this is worth endangering my health, possibly dying

#CovidIsntOver #Covid #CovidIsNotOver #Immunocompromised #Disabled

[Joanna No Banana @JoannaNoBanana]

I heard someone refer to being covid cautious in 2023 as “playing the long game.”

That’s exactly what it is.

Yes, it’s rough to miss out while we watch others move on but not everything is always as it appears anyways.

[Charis Hill | they/them | 🇵🇸 😷 @BeingCharisBlog]

[Ableist slur used against OP mentioned]

The right to wear PPE, folks. We're fighting for the right to wear masks now. The bar is the floor and we're still under the basement.

This is just example number infinity that disabled people have tried to tell you would happen.

[Hate my guts @IBDcanSmyD]

@BlackIncBooks @oshergunsberg I'm 30
I'm only now going thru the process for autism&ADHD diagnoses
I don't have formal ones, but that doesn't make me any less autistic, ADHD, or neurodivergent
This sticks a label on what's already there
Getting a diagnosis is hard for anyone not cis AMAB/acting like Rain Man

[Hate my guts @IBDcanSmyD]

@DrAshleyDenmark I am so, so sorry for the loss of your beautiful girl. No parent should ever have to go through what you have.

I am so sorry that the healthcare system failed you so appallingly. It is absolutely disgusting. I'm so sorry that yt doctors didn't listen.

💔

#VivianMonroeStrong

[Hate my guts @IBDcanSmyD]

Too often, POC needs are not met. Too often, this is fatal

POC parents should not have to pick up the slack from yt drs. This is disgraceful

Healthcare is a human right! Affordable, easily accessible healthcare that LISTENS is essential!
Help if you can:
https://t.co/VWKtcW8ZIP

[Ashley Denmark, DO, MS (she/her) @DrAshleyDenmark]

My daughter Vivian died
My heart is broken
👩🏼‍⚕️👨🏼‍⚕️ never listened to me ….
👩🏾‍⚕️I had to do my own research & discovered that she had #EDS #MCAS that required a different treatment plan.

The U.S. medical system is biased + broken #WeDeserveBetter #VivianMonroeStrong 🌈🌈🌈#Forever5

[Hate my guts @IBDcanSmyD]

Read through this thread. This is what families of colour experience when police are involved. They're lucky they all survived. We know the track record for LEOs and POC.

#BLM #BlackLivesMatter #PoliceBrutality #Racism #Racist #ACAB

[Hate my guts @IBDcanSmyD]

Medical wearables! I feel so seen 😭💖

#TheSims #MedicalDevices #DisabilityTwitter #Disabled #ChronicIllness #MedicalEquipment #DisabiltyRepresentation

[The Sims @TheSims]

A base game update is here with new content including medical wearables, binders, shapewear, a light switch & more including bug fixes & console gameplay improvements 🥳💚

Read more about today’s update in the latest patch notes! https://t.co/4c4vZdfWBY

[Hate my guts @IBDcanSmyD]

100% this. I have been self isolating since March 2020 (Dr recommended) for my compromised immune system. If I have to go out, I mask

I've missed out on so much because I don't need more health issues
#AutoimmuneDisease #DisabilityTwitter #Disabled #Immunocompromised #Disability

[Charis Hill | they/them | 🇵🇸 😷 @BeingCharisBlog]

Hi.

Disabled (including immunocompromised) people don't feel left behind by your pandemic ableism.

We. Have. Been. Removed. From. Public. Life.

That's not a feeling. That's a fact.

And we have feelings about the fact.

[Hate my guts @IBDcanSmyD]

@DoomNails And, you know, helping those who struggle, rather than sitting on my greed hoard like the worst dragon ever

[Eric Feigl-Ding @DrEricDing]

Wearing a mask prevents you from getting enough oxygen and prevents exercise… not.

#BringBackMasks

[Hate my guts @IBDcanSmyD]

@adisabledgirl Legit, the support from the disability and chronic illness community is vital 💖

[Hate my guts @IBDcanSmyD]

I constantly joke that I'm so high maintenance, I'm a full-time job.

Managing my health IS my full-time job, but worse. I get no weekends or holidays. I can't stick it with a babysitter for a night off. I am my own nurse, admin, and more
#ChronicIllness #ChronicPain #Disability

[A Disabled Girl @adisabledgirl]

It’s a shame more people don’t understand how much effort goes into living with a #disability and #chronicillness 🥺

[Hate my guts @IBDcanSmyD]

@adisabledgirl It absolutely is. Thank you, it's hard, but easier together. You stay strong too 💖

[Hate my guts @IBDcanSmyD]

I get filthy looks/abuse when I use disabled parking spaces without my mobility aid. I have the permit clearly displayed but it doesn't seem to matter 🙃
A lot of disabilities are invisible
#Ableism #Disability #ChronicIllness #AutoimmuneDisease #ChronicPain #InvisibleDisability

[Charis Hill | they/them | 🇵🇸 😷 @BeingCharisBlog]

Them: "You don't look disabled."

Me: "Huh. You don't look nondisabled."

[Hate my guts @IBDcanSmyD]

This! I lost my dream career.
I had my dream job & I loved going to work every day. I went early, stayed late & loved every second
I'd rather be working than spending all my time managing my health. It sucks. I'm not a lady of leisure, I'm my own nurse
#Disability #ChronicIllness

[Nia | The Chronic Notebook @chronicnotebook]

Please know that if someone can't work due to a chronic illness or disability that's not a good thing. It's not living your best life and enjoying your free time. It's actually giving up on career dreams and having no financial stability. Please don't glorify it because it sucks.

[Hate my guts @IBDcanSmyD]

It's important to fight for equal rights across all categories. We are not truly free, until we all are free. I stand with Iranian women ✊️

#IranProtests #IranProtests2022 #IranianLivesMatter #IranRevolution #Iranianwomen

[Swara Bhasker @ReallySwara]

Received via what’s app.
Forwarded many times.
#IranProtests2022

[Hate my guts @IBDcanSmyD]

I'm an ambulatory mobility aid user. Some days, I can get around the house okay without it. Other days, I can barely walk to the bathroom across the hall from my room

#Disability #DisabilityTwitter #Disabled #ChronicIllness #ChronicPain #AutoimmuneDisease

[Hate my guts @IBDcanSmyD]

As an immunocompromised human, the pandemic still has a huge influence on my life.

Sure, we all have COVID fatigue, but COVID doesn't go away just because you're sick of it.

[Charis Hill | they/them | 🇵🇸 😷 @BeingCharisBlog]

It's literally still a pandemic

[Hazie Thompson @haziethompson]

Here’s a short list of what I’ve lost since acquiring a chronic illness.
My business
My family
My friends.
My dog
My home
My autonomy
But all that ‘attention’ I get has more than made up for it!
Look at me, jet setting from bed to bathroom!
Paying my bills with likes!

[Charis Hill | they/them | 🇵🇸 😷 @BeingCharisBlog]

Also? Stop praising people for openly using accessibility tools.

Yes, masks are accessibility tools.

Stop praising disabled people for wanting to survive.