Angry Guts Profile picture
Jul 21, 2018 18 tweets 5 min read Read on X
I’ve spent over half my life as a sick person.
I was diagnosed with aggressive ulcerative colitis at 11 years old. I had a colectomy that resulted in an ileostomy at 13. I completed my surgeries with a completed J-Pouch at 16. 1/?
I have retained all of the side effects of having an autoimmune disorder. I also deal with issues with my pouch on an extremely frequent basis. As is common with inflammatory autoimmune diseases, I have chronic issues with my joints and with pain. 2/?
I have a diet very limited to what healthy food I can consume. I have a body that either through pain or fatigue or illness has a hard time remaining active. Everything in my life is just a little bit harder than it would be were I not disabled. 3/?
I live with medically induced Post Traumatic Stress Disorder, as well as depression and anxiety. A lot of my life is avoiding things that make me sick or make me hurt as a result of my PTSD. Whether anything is really happening to me or not, my pain is real. It feels real. 4/?
I have nerve damage in my back due to having had an epidural cath break while in my spine, and from hospital neglect. This makes standing for long periods difficult, and stiffness a problem due to pain from moving. My hands are extremely sensitive, and while I’m 5/?
Blessed to be able to use an ergonomic method to type at work, in using my hands for other things (carrying things, washing dishes, typing on difficult keyboards, etc) I deal with a lot of joint pain and stiffness. They have not been able to diagnose or treat this yet. 6/?
My knees are probably my next worst joint situation. I occasionally go through periods where I cannot walk without crutches due to extreme pain in my knees. Due to my illness being digestive, I’m almost always nauseous. 7/?
Due to my nausea and heightened sensitivity to things like taste/texture, sometimes, I need things like straws to help me more easily control what I’m consuming, and the method to which it’s transported to me. This is not constant, but it does happen. 8/?
Due to the pain I have rendering my hands unable to do some simple tasks like cleaning and cutting, things like pre-cut fruits and veggies make it possible for me to cook meals (very over cooked fruits and veggies for accessibility; small pieces are a must) 9/?
Sometimes, if I’m in a REALLY bad flare situation where I cannot do ANY dishes, or don’t have someone to help me, I don’t have a choice but to use paper/plastic plates, bowls and utensils. This is how I can survive. This is what the result of my disability is. 10/?
Before my pouch got to the nearly unusable state that it’s in, I was a vegan. I didn’t eat any meat or dairy. My grains were ethically sourced. I educated people on the benefits of veganism including those on the environment. I have a huge heart for this planet. 11/?
But you know what else? I can’t help the planet if I can’t live to be part of it. That’s why I need some single use plastics.

No disabled folx that people are reprimanding want to attack the environment. We simply wish to survive. 12/?
And just like we have tried any and all alternatives to treat our disability symptoms, we have tried and considered alternatives to our plastic usage. They do not work. Everyone has a different reason, but a common understanding: we are doing our best to live our lives. 13/?
We do not need suggestions. We do not need advice. We do not need anecdotes.

We need you to trust that we know ourselves, and that we are doing even just the bare minimum to continue existing.

We need you to hear what we’re saying. 14/?
Performative activism is not progressive and it certainly isn’t helpful. You are doing no good for the planet when you plan to slaughter its people.

You speak from a place of privileged long left unchecked, and need to listen to the education being provided to you for free. 15/?
I just spent a lot of my time (remember, hand pain) and sacrificed any of my privacy to explain to you why single use plastics allow me, a disabled person, to survive with a significantly lower amount of burden than I would without them. 16/?
But you shouldn’t care about these issues just because they may affect you or someone you know.

We are humans and we need to work to make sure that our fellow humans have what they need to live. This has, historically, been the main reason human beings have existed so long. 17/?
I told you why I use plastic.

I told you why other people use plastic.

I told you why you should care.

Now run with it, and continue to learn from disabled people and our experiences. We need it.

#StrawBan #Disabled #HandsOffMyStraws #Plastic #Disability

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More from @ShutUpDanni

Sep 25, 2020
As we battle the ever present “what about personal responsibility?!” healthcare argument, I’m here to tell you: it doesn’t matter.

I’m disabled. I didn’t become that way by my own hand - it was entirely an accident, and I was a child doing child things. But here’s the thing: 1/7
That does not make me more worthy of accessible care.

Whether an illness or injury was caused by genetics, accidents, heroism, alcoholism, drug abuse, poor eating habits, lack of exercise, it literally does not matter.

Human beings deserve to get care when they are ill. 2/7
EVERYONE deserves care when they are ill, and I do not care if they are someone working 80 hours a week to make ends-meet, someone living under the poverty line on disability benefits, or rich enough to take care of it even at its current ridiculous price - EVERYONE. 3/7
Read 7 tweets
Jul 11, 2020
Okay, I’m gonna give a quick story time.
I feel that some of you are still operating under the pretense that “I’ll probably survive COVID, so I don’t have to worry.”
You do.
Because the fact that fully healthy, abled, young individuals have died as well aside, you are 1/7
forgetting the fact that illnesses don’t leave without leaving things behind.

I know this firsthand.

I had pertussis 8 years ago, when I was 18. My immune system was very poor at the time (and remains so).

Prior to getting pertussis, my lungs were VERY strong. 2/7
I was a choir student from when I began school until I finished. A soprano who trained and competed whose preference was opera. I was also in a band and sang acoustic pop punk covers, almost every weekend. I had also been an avid swimmer most of my life. Once the weather 3/7
Read 7 tweets
May 4, 2020
Friends, propaganda has sprung to using misleading statistics as per usual, so as an ex-sales associate, let me put it in perspective for you.

My mother in law’s conservative radio show is trying to downplay COVID by stating that the death rate in NYC is ONLY .01% 1/4
Sounds small, right?

NYC has a population of 8,398,748 people.

.01% of that number?

About 840.

That is 840 people, dead. 840 people with families, friends, memories, dreams, futures that were torn from them.

If you hear statistical propaganda, please do the math. 2/4
It’s a common trick to try to present percentages in a dismissive fashion because it seems smaller.

In sales, we’re taught to talk in money, because $100 off $1000 sounds a lot sweeter than 10%.

Don’t be fooled - these numbers are NOT small.

And even if they were? 3/4
Read 4 tweets
Apr 20, 2020
CN //// drugs
.
.
.
I live in an area that is pretty much a heroin hot spot. We’ve had 4 (if not more since I last saw reported) overdose deaths during this time. And every single comment from locals on the matter has been nothing short of heartless. 1/6
As a disabled person, I’m not new to the cruelty of human beings. I know exactly how shitty people can and will be to each other in any given circumstance. But this is just too obscene for me to deal with. This is HARD. Quarantine, COVID, this situation is hard for EVERYONE. 2/6
Imagine how hard it is for those who were already battling such terrible demons. Imagine losing your support lines and being forced to be alone with nothing but your pained mind. This is one of the worst things that could’ve happened to those in recovery 3/6
Read 6 tweets
Jan 21, 2020
From reading @coffeespoonie’s saga on the inaccessibility of Uber drivers refusing to follow the law, one of the hottest takes I’ve seen so far is “you should have to identify yourself as disabled before using any service.”

No. We are not doing this. Here’s why. 1/6
Abled people enjoy ignorant bliss in the form of “nobody would willingly discriminate against disabled people”, but it happens. Every. Single. Day. This is our lives. Why would you suggest that disabled people sign themselves up to be discriminated against ahead of time? 2/6
This is why:

Whether it’s conscious or subconscious, you do not see disabled people as people. You would rather we not exist in society with other people. You’re “fine with us being disabled” (as though we had a choice) but you want that kept far away from you. 3/6
Read 6 tweets
Oct 3, 2019
CN // Medical Abuse

Just read an extremely disturbing and triggering article about hospital staff creating a miniature “Wall of Shame” based on patients CONFIDENTIAL MEDICAL RECORDS, making fun of disabilities that they found funny for some reason. 1/5
This was triggering because I have an “embarrassing” disability. I’m one of those people. And I already have an extreme aversion to hospitals and medical facilities (to the point where I have almost died because I refused to go in for care due to such extreme anxiety). 2/5
To read something like that reminds me how little people think of disabled people, like me. Reminds me that no matter where I go, I will always be mocked, even by those I am entrusting my care to. People who do not have to wake up every day facing the hell that I face. 3/5
Read 5 tweets

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