Voices Rising from Silence (PTSD Trigger Warning)

As an advocate for myself and when I can other people I run into a question a lot. “How do you do this?” This question most often comes from my fellow autistics. As someone diagnosed as an adult I find a lot of my experiences without diagnosis mirror the “medical treatments” others on spectrum who were diagnosed have. Child abuse in disguise as therapy in order to teach control reigns the autistic childhood, we learn silence. We learn stillness. We are erased with in our own bodies as much as possible. We are punished for existing. The best autistic parents even do parts of this because there is no voice that they hear, yet, from the autistic community. Our song has just begun.

The autistic culture is one of enforced shame, it is one where we deal with a lot of hate just for being. This is in part due to a lot of hate organisations like Autism Speaks, who sink their budget not into helping people but into quackery, negative ad campaigns and convincing newly minted parents of autistic children that their children are a burden. That their children will never live on their own, get married, have a “real job”, or anything that is valued as productivity. These parents are convinced that there is only pain in the life of the autist. So they create more of that pain, feeding it. I do not deny that a lot of things with autism really suck but I LOVE who I am.

How does one learn to speak? I think this how to might apply to survivors from many types of abuse. It is about regaining the voice. This process is not universal and is a general guideline to what I answer the most often when people ask me how I blog, how I advocate, and how I risk going out of my house being so far from the norm. I think I hide less and less of my abnormality. I celebrate it now, but it is an on going process and journey.  I wish there was a universal answer but here is what I worked out as far as what I do subconsciously and consciously that I can put to words.

1. When I want to be silent out of fear, I speak up and risk the consequences. This to me is the basis of self advocacy. Oppression is born in a culture of fear, so I must not obey the fear that tells me to be quiet. “If you are good and quiet nothing bad will ever happen.” If that was true I would be a far different person, because being “good and quiet” only lead to pain. It leads to secrets. Good and quiet would mean still being with my exhusband, it would mean watching my father murder my step brother with a frying pan, and it would mean condoning every act of rape, malpractice and other harms brought to me by people who tried to take advantage of my selective mutism, of my physical fragility and of my silence. Sometimes it is a small noise, other times it is a roar. Sometimes it is actually words. Sometimes a song. I am not silent. Not anymore.

2. When I am threatened, I do not revert to silence. Making noise leads to punishment. It leads to the threats that come in a variety of forms. I had a medical professional threaten and then withhold my pain medications on more than one occassion, because she did not believe I was not addicted. I suffered. I was then told if I kept speaking up to her boss about these threats and punishments she would have me black listed. I took that threat to her boss and switched doctors. I have a doctor now in the same facility. I wanted to be silent. She is no longer my doctor but treats others, thus I also am in the process of number 3.

3. Do not let the threat harm others. This is a mixed bag. The threatening person may be someone you cannot stop. This protection must never come at a cost you cannot live with. This means do not chase the axe wielding halloween monster, go for more qualified help. It means talking to someone’s boss, documenting issues. This is often what gets me to perform step 1. If the doctor was allowed to bully me with medications I needed and threaten my life that way, she would be allowed to do that to other people who may not be able to endure it, be able to adapt and if someone else spoke up without documentation I had, then I was harming that person. Thus i went to her boss in step two. As you can see these steps are not in order because they are more a mobius strip how to guide for living.

4. Document the threat. Little notes from my exhusband, recording the doctor without her knowledge as it is legal to do in my state, pictures of bruises. Those parents who send their autistic kids to school with hidden cameras and find out that not so shocking to any of us, abusers aer out there ready to harm your vulnerable chiild for being who they are.

The same process applies to why I write. I cannot put on a super hero cape, race about the world and fix it. I must slowly advocate for myself and then when I can on bigger projects.  I cannot advocate for others if I do not come first. i think back to my first few tries at blogging. I threw on a secret identity, I tried to hide who I was. Yes, there were other blogs before Textual Fury caught fire. I stumbled, I struggled with my words out of fear. Then I realized that was what i was trained to do and the rebel that lives in the core of my being took over and I wrote the first post here. As I wrote more and more the tone of my blog changed and I let out the “monster” i feared. It turned out that person is pretty darned cool and I began to push further and further out in the world as myself. I never hide anymore.

So how does someone conditioned their entire life to a culture of silence learn to speak? By doing. The posts I never share, those still happen, the poetry saved on my hard drive instead of published, facebook and talking to friends, gathering with other autistic people. Knowing what I know now those are just little things. It has to be something you want, so you have to stop hiding from the desire to write, to sing, to speak, to shout to be. The thing is? Just wanting to IS enough. When people ask me for help it makes me proud, not of me but of them. I am proud of every single person who takes on the difficult journey of learning to speak for themselves. This is not a challenge exclusive to autistic folks, though the culture of silence caused by shaming and abuse seems to be so prevalent among my people that there are no autists I know without PTSD or that they know. There are no autists without pain, suffering and a knowledge of abuse that is intimate and too close, that I know of… except perhaps those children being born right now. So we are learning to speak so that they do not face the battle of a life where our words are forced back down our throats until we choke on them. That is why I wrote this out. The how to on blogging is the same as other things. Baby steps, do what you can and try to do a little more each time. Cry, laugh, feel happy, feel good, struggle with it. Live.

I think of the others who came before me, for I was hardly the first blogger with autism out there. My brain does not want to write names but I can see faces, words piled up before me that create a beautiful sky and world. I remember the first moment I read something by autism speaks and it broke my heart and filled me with fear. Was I seen as such a monster? Did i deserve the abuse? I was a baby back then, not yet a woman and lost in a world of flying diagnosis where everything seemed to stick. Then I decided to find adults on spectrum too. Now I have loving friends who hold me close, even if it is just as text. Better as text since I can enjoy that. The diagnosis that stuck saved me so I could find out that no, those descriptions of horror are wrong. Even if I had never been able to live on my own, they are wrong. There  should be no shame in having a need. There should be no shame. So i am writing this for the people who inspired this post by speaking,by learning to speak, by asking, and by being.

Will I… (Trigger Warning)

 

I have been trying to hold back my level of suffering from the world. The various support groups for autism, Ehlers Danlos Syndrome, PTSD… every single one this is a reoccuring theme. I know why. Not only is being in this level of pain dangerous but it makes you vulnerable and often this is when people abandon you, attack you, or they cannot comprehend what you are trying to tell them. I do not as a rule cry when I feel so much pain but I silently sit and try to find the cause to fix it or I just learn that this is my new life. I must always be prepared for the permanence of my agony. There are people who are lucky enough that this is not the case.  I cannot stop hiding this, even when I try sometimes. There is the element of fear. If everyone knows that I can barely breathe for pain, then even the predators know. (Oh hello predators. Yes I will tazer you even when I hurt.)

This song is from rent, it is called Will I… thus the title of the post. I could die from the on going issues I have at any time. My heart could fall to pieces, a literal broken heart. I could have a heart attack from my stress and high cholesterol. I am bleeding internally somewhere, I could run out of blood. I could kill myself. That is why I am writing this post. You see, that is the whisper in the depths of what might be my soul. If I die it is over. I do not live out of some doubt about an afterlife. I do wonder but that is not a consideration in any of my choices. I do not stay alive for other people or the cats. I love many people deeply, so deeply there is an ache of joy. I guess a mental pressure sore from all the goodness. I stay alive because I want to.

I am afraid of dying and missing people. I am afraid of lingering in pain without dignity. I am terrified of being tormented by doctors as Ihave been lately. The nightmare is not the diseases or the pain. In fact some of that is better. I officially no longer am diagnosed with epilepsy but still have a seizure disorder of some sort. The some sort is not defined by science. Yet NOT having epilepsy is a miraculous thing.  It is a wonder to me.

I spend a lot of time advocating, and passionately burning for the world. Now I am just burning. The pain is in every nerve, even though some of them should not be communicating with the brain. My blood pressure is up, my heart is racing, and this is omnipresent. I have had to fight around government shut downs for my needs, but I did this. Yet all I want is to have someone hold me. Something no one can do at all. Maybe ever again. I just want to be held in a soft space of beautiful harmonics without actual sensory input. This dark space has no reality. I often find this song in the undercurrent of my psyche because it holds most of those things. Yet I do not have to wonder. No, my life will never get better. I will always have some agonizing wrong. Yes people care. I have never known how much people care, I think I do then it seems to grow. Maybe I grow. Maybe not.

I am terrified. I feel the race of time, not just because bleeding internally is very bad but I need this resolved for my mental health before november. My PTSD is at a peak height and I am not sure what I will be enduring medically but I know I will survive it if I can. Will I be allowed dignity is the true question. I am afraid to die and leave people I love, this is new to me. I never cared before. I always lived for things like spite, revenge. My revenge has been to build my life up into something I was told I could never have. I look around this space I live in and every corner has a marker of love. Every doll I own someone else gifted me, the Gothmas tree that needs its decorations and makes Sylvani happy, the pile of scarves I know will be useful and necessary that are clean, the myriad of tiny touches. My life has been a life of grief and loss. Now that I have things I want to hold on to I am afraid I cannot survive this. It is not a lack of will to live, it is a lack of trust in my doctors. I have no faith in even the best of them. Why should I with the ineptitude I have fought against for so long?

So I am left to wonder. Yes, I am in pain. No I do not know if I can survive this. I will try.

One more thing: The man who wrote Rent? He died from a condition similar to EDS called Marfan. That runs in my family too but I lack the features that mark it. That is LUCKY for me. I sometimes wonder if the pain he felt and held too close contributed to his dying, if that is why Rent hits the notes I sometimes NEED. Just a little tidbit for people who may not have known.  I do not reach for the anthems of survival that are broad and direct, they ring hollow. “I will survive” does not match my spirit. Even when that is indeed the attitude that I display as I emulate the bronco and buck for my life.

 

I am jagged glass

shattered now

pick me up

fear the cuts

I do not intend

Yet I broke

can you lift me up?

Will you laeve

I am broken

Never repaired

yet I was beautiful

I am beautiful

Shattered glass

so many sharp edges

yet it is true

I am beautiful

I AM More Important Than Your History

Random thoughts as I woke up this morning, and began my daily motions crept into my head. I have been thinking about the acecssibility of my city, or the lack there of. The excuse I am given in new buildings is that the sticker on the door should be enough. Some places obviously tried and usually it shows in grand ways. Other places give the excuse that to put a ramp in, or wide enough doors would be destroying the historical importance of the building that their business sits in. I am more important than the history of the world. All people are.

I know that this makes me appear to hate history, yet this is the opposite of truth. My first passion in life was history and I have always loved taking part in reenactments. I am for preservation but not when the preservation includes the history of excluding others based on arbitrary things such as skin color or ability. I suspect that the place I live is far from the only one guilty of such crimes, yet I look at the excuses and they no longer work.

The first time I approached a historical building and there was no ramp, the excuse worked, because then I did not know my rights under the Americans with Disabilities act. The second time I was told this, the excuse did not work but I had no power. Since then I have regularly avoided the section of town that is considered somehow worthy of preservation. Even going along the side walks outside is difficult as the inclines on the “accessible” places are so steep my power chair cannot make it, and coming down the other side of these inclines would likely be an act of suicide. Old Town is lovely, and often has events that are free and meant to gather the entire community. These events only count if you are willing to burn out your chair engine, sink into grass, or sit on the only part of the side walk that you can get to that is safe. The excuse is history.

None of these buildings retains their original purpose. They are all shops selling the same tourist crap. There are a few restaurants but they too are selling the tourist crap. People claim native ancestry and sit out on the side walks, because this is apparently historical too and barricade the way. I have had people get angry at me for asking them to move so I can go past. Then there is the staring. For some reason people react more strongly to my presence in this section of town. The idea that a disabled person may be near these expensive shops, may want to see some old time gun battling, or in general may want to be on the side walk that has curb cuts at BOTH ends (an extreme rarity in this town no matter the section) boggles their minds.

I have found my response finally, for why they need to have access for me and others who are disabled. I am more important than your history. It is not my history if I am prevented from learning about it. It is not a history I can embrace when a store that is selling the same tourist thing as the one next door can have stairs and no entry and their excuse is history. I realized this morning that the lie does not work for a very simple reason.

All of these buildings have restrooms. Every single one has a place to go when your bladder is full, when the tourist trap food gives you a stomach ache, or when you need to check your make up. Every single one. All of these buildings were built without restrooms. Every single one. They were built with out houses in the back, all of which are torn down. If access is less important than poop, you are obviously not thinking straight. If you prize history over poeple, you lose vital lessons about people that history contains. Yes, the stories here are amusing, amazing, and important. So are the people who want to hear them and might not be able to.

So there it is, my reply has been cemented finally. Whenever someone plays the history card in this never ending game of poker for bigots, I have my answer. If you can put in an outhouse, you can put in a ramp. I am more important than your history.

The Good The Bad and the Medical Drama

(This is the third time, my internet ate this twice now)
ahhahahaaa Woh woh woh… (theme to the Good the Bad and the Ugly)

Woh woh woh woh….

For those of you who have either never heard this before or just want to hear this while reading here is a video. For the hearing impaired the them is pretty much what I wrote above.

Today I saw the gynecologist about the font of blood issue and the discussion was as I expected. Though to get there I had to nagivate the world and I woke up feeling a bit fired up. I was going to make them see me even if they tried to screw up. I was prepared. So I donned my hat, today’s selection is my black riverboat gambler hat (the bad guy’s hats in every western or gambling movie) I put on make up so I could try and feel at least a little okay, a barrier between all the crap and myself, and went out. I had to take the sunshade off because the transport vans are too short for it, so I was hiding under the hat and sleeves. The ride was okay but the driver was obnoxious, though I enjoyed making him squirm with my honest answers to his invasive questions including, “Oh crap was that rude of me?” I also explained the ADA to him in detail and by the end of the half an hour journey he was very quiet and thanked me for not being mean about his questions. I shouldn’t have enjoyed that as much as I did but I was being straight forward and honest. He did ask me if I thought all technology exists because of disability and I said at least most of the things he takes for granted such as automatic doors and some things on his computer do.

I went into the hospital and popped into the elevator, went up and was immediately surprised that they had renovated the floor plan. So, I turn around and there’s a receptionist waiting to answer my questions. She is here as her first day and doesn’t know where I am going but goes to ask, returns and leads me as far as she can, I read the sign on the door about an alarm and go to back track but a tech saw me and was surprised I didn’t ignore the sign and make loud sounds. I pointed out there is a sign on the door and she said “Well in the two years since they installed that alarm you are the first person to read it.” The last time I came this door was pinned open. I am sure other people read it but they didn’t care about how it would effect other people. I sign in, noting that in this room there are children and pregnant women. One of the little girls is scared, and I am instantly triggered because there is really only one reason I know of for a five year old to be in that office. Heart broken I scribble my information, my eyes letting me read paper today.

I sit and turn my music on loudly, drowning out all but the barest sounds of the room. I don’t want to hear the joys of the pregnant women, nor do I want to hear the sorrows of this child or the frustration of the teenager who doesn’t understand why just because she had sex she has to go in. I did anyway but I tried to be respectful of them because my brain would leap and bound and I will never forget their secrets. Ever. I will try but I know that next time I see a little girl of similar appearance I will think of that girl who looked so much like I did. I think that was what startled me the most. No one, as usual, could tell that something was wrong. That’s what I want. I want people to not be aware that my brain has me in a tail spin where I suddenly connect the new changes in my dreams of demons because of a child’s words in pain, pain she should not feel.

I am pulled out of the dark thoughts by a little boy, I didn’t hear the door and that’s the point of the headphones. Doors make me jumpy and I had parked with my back towards it because that was the best spot for me. I needed to point away from people so I could focus. “What’s that mommy?” “It’s not nice to stare, that’s a wheelchair.” A few moments passed and he was there beside me, “Are you a cowboy?” Not the question I expected. I look up and I can tell his mother is tense, her body is tight and she seems upset. I may have misread this but I instead told her son, “Nope, are you?” He shook his head and rattled of historical details, I could match him and we had a geek fest in the corner. His mother,who I am still watching comes over and asks me why I am willing to talk to him, as if there is something wrong with her son. “Well he started it.” She seems confused by my answer and asks him why he was willing to talk to me. He shrugs, “She’s nice.” His mother now seems worried and tells me he is Autistic, I tell her that’s why he is willing to talk. I am too. I doubt she got why he could talk to me. She seemed stuck on his idea that I am nice and safe when he doesn’t know me. All black head to toe is threatening to the Nuerotypicals, and heavy eyeliner? Crazy goth wheelchair lady appearance doesn’t get nice from them.

I am called in, I wave goodbye to the future cowboy and go into the back. I am lead down a yellow corridor, I am sure there are pictures but I only see yellow, it’s not a bad shade but it is not a pleasing shade at all. It stabs the eye like sandpaper with it’s shade. I had scheduled a specific room because of my disability, and this was not the room we entered. This room was tiny, the door opened and would hit the patient if said patient were on the table which also doubles as Mount Everest. The nurse is confused by the idea of closing the door behind me since I stopped in the middle and look at her and tell her, “This isn’t the right room. I am supposed to be in the procedure room.” It was supposed to be written down but Dr. Receptionist didn’t do this either. I feel frustration, but I am trying to work with people. She goes to check. I try and find a way to park my chair, visualizing first for safety and no, there is no way this room can fit me and a doctor and I won’t park in the yellow hall. That’s not safe for my equipment which I need for daily living.

The nurse comes back and says that they are waiting on a call in to the patient scheduled in that room in a half an hour but leads me to it, because there is no other way. Which is why I specified when I called in, and asked for the accommodation again. There is no other way even with an army of nurses that room will work and the others are full. The procedure room is used for the disabled and cancer diagnosis. It’s no a pleasant room and it effects the nurse. I can tell this. That’s not good but I noticed this last time. There is trepidation with this room. I don’t understand that, because cancer diagnosis can save a life that is lost without it so it’s good. The cancer is the bad.

I am told I can change, the patient isn’t here yet and said it was fine with her to wait. I am honored by this because waiting to know if you have cancer is tense, scary and I have done that a few times. I trade pants for a sheet and perch on this table, which is a safe distance from the ground so if I bungle this? I am okay. The doctor comes in. I find her oddly short. She is kind and we discuss my symptoms and she agrees with my theory that the lining of my uterus got to be too thick and tore things that shouldn’t tear. So we proceed with the testing.

I hate this part because it’s awkward, I feel self conscious and they poke you with sticks. I don’t know of any procedures for men that include as many sticks as when I see a gynecologist. Q-tips are sticks. The biopsy which they attempted to perform includes more sticks. The tool is a stick that sucks things into itself, which is better than cutting. The biopsy failed because my uterus just wouldn’t let anyone in. I did tell her I was having cramps still, and she warned me they would be worse and even the attempt at the biopsy causes bleeding. Which I knew going in, from the last time. It was unpleasant but instead of a hysterectomy there is one thing to try before we go that route. This is good.

Provera and Metformin are both known to force a period in women with my conditions. I cannot take metformin, so we will try provera when I don’t have a period by January. She says if. I know better. I don’t have a minimum of two periods a year and that is part of the issue. My body will let itself go for years, a part of me is fine with this for obvious reasons but the side effects are bad. If I didn’t eat a diet of meat and meat with a side of meat, I would have needed a blood transfusion in the ER from blood loss and my doctor was upset that they did not run all the tests they should have including an ultrasound. I will be getting one of those for my birthday, as three days before said birthday next month I have the appointment. More unpleasantness but I’ve been there before. The worst part is having to pee while they use more sticks to figure out what your guts look like.

I should have been admitted in the ER, at least for observation but I think that was clear from my symptoms. The doctor asked if I was considering suing, and I did not answer. I know I can and I am going to try working with the hospital first to prevent more bungling idiocies in their future. I don’t know that this is possible. I have to try.

I am still stunned at the differences in level of care, but at least in the last ten years there has been a shot at a treatment. For ten days in January I will take provera, this will trigger a period. IF it fails to do so then I get the scissors treatment. I think I know what will happen, and it ends in snips. However, I could be wrong. That feeling in my bones could just be my frustration and tiredness. I am tired of being tired. I am tired of not being able to eat food. The good news is having a period every six months should reduce my acne, abnormal body hair issues and may stop my voice from dropping anymore. I used to sing soprano and now I am an alto. Even when I speak my voice is lower. The one bonus is also a curse in some ways as I have a “male” sex drive, as in the way I desire sex has altered itself. There isn’t a slow cooking of want and thought, there is instead a visual and then an instant need. We discussed this too, I don’t know that I want the ease of pleasure to go away but cancer is bad. Especially cancer in your body where they would have to cut you wide like a fish. If we do a preventative hysterectomy my chances of healing are better. So that’s the plan, if this drug fails then we cut out my sugar and spice. Well at least the sugar. Spice and everything nice should remain, as will at least a remnant of a puppy dog tail.

I have been preparing over the last six months for surgery. Not a specific one but there are several broken things which the only fix is to either leave it be and suffer which won’t work forever or surgery. I have three potential surgeries. My jaw, my uterus, and my spine. Someday they might want to cut around there. So I am gathering things to keep me going when the time comes. The fact that I have avoided most major surgeries until this point is quite amazing medically speaking, because of how much of my body works “correctly”.

I am even working on a plan for Sprite and Nymph. My fear is Sprite’s needs not being met. My having been away for hours today has her draped over my knee, a white hot sleepy kitty. She needs me. I need her. My doctor having anaphalactic reactions to cats doesn’t help things either. I am not resigned to surgery but would rather that the provera works however that is not what my body tells me. At this point I hope that sense is wrong but it has yet to be wrong. I will know before this time next year if it was right and that is enough for me, at least for now.

I will not miss having a goatee if I don’t shave. I will not miss cramping even after the period is over. Both of those should go away with a “withdrawal period” as the forced period is called. My doctor was shocked and called it malpractice that no one had even tried anything in the last ten years because both of the aforementioned drugs are not that new, sometime with in the last five years they should’ve been brought up. Metformin was tried for a non uterus related ailment. Doctors are so tiresome at times. If all doctors followed their own protocols so much would be better. They are simple little things that are ignored and often make the difference.

I am too tired to be angry but I am very disappointed. There is a sense of betrayal here with in me. I trust these people to protect me from my body but they do not. Yet this is what I expect of them too. I have that sense of wanting to just flee this state again. If I could land safely anywhere I would go right now. I wonder if that urge comes from the growing knowledge of just how broken this state and it’s systems are? I am not sure. I just know that my future isn’t set in stone and I am hoping that no one tries to argue with me about having a kid first. I am sterile anyway, but I was told today that medicaid will pay for me to get my eggs scraped. Since that’s just what medicaid should be covering? I almost cursed.

The doctor as she poked me with sticks, for some reason female medicine is an endless line of sticks, she brought it up. She said she has to make the offer. She didn’t seem shocked at my scoffing at the idea. I don’t understand this however. I also am left trying to imagine medicine for women if we were men. There are similar men’s issues to my problems but they have all sorts of treatments from the physical non surgical to a myriad of drugs. Why is it that my medicine for my body has to be archaic because I have a vagina? This is illogical nonsense. The patriarchy just screwed me vaginally, that was my literal thought when I had that revelation. If in ten years the only thing is another form of BIRTH CONTROL? That’s IT? No one tried some sort of other thing? I have ideas that could help medically I think but I don’t have the science to know if I am right.

Once more they have me wanting to go to school. Once more they have me feeling frustrated. I was triggered and in pain and again had people questioning if I hurt as bad as I say I do because I am not screaming. It is exhausting navigating around these iron poles of nuerotypicality. How do they expect me to react? Does everyone have to scream and cry like a baby?

Oh yes and I had an allergic reaction to betadyne in my cunt. That’s not pleasant but not as bad as latex. Turns out that the ER should have also asked if I am allergic to shellfish, and as I haven’t used betadyne in years and always was sick anyway when doing so I didn’t know. The reaction is minor, just a rash and my doctor was very quick to treat it and change the sterilization stuffs but still. Why wasn’t that question ever asked before? I know that shellfish and eggs now have to go on my allergies list for the short list or I am screwed and rashy.

I am going to cuddle this ball of fur named Sprite, she’s currently in her dreams but her body is adorable and soft. Her paws are hanging off into space, her body is curled against my leg and between the two of them and she looks like she is smiling. She isn’t snoring yet but I am going to hold her for a while. I haven’t been able to do so for the last month due to cramping but she is worth it and I think I need her too. After all she always treats me as a person and loves me, with her I don’t have to be stunned at the rarity of a doctor or nurse who realizes I am competent and independent. Even if that happens only once they realize I got to the table my self, without their help. I changed and did it all because I can do it on my own mostly, and the nurses weren’t willing to assist me so I dealt with it to get on with my day.

Not All Expectations Are Positive. (Trigger Warning)

Nymph taught me something. I didn’t really know the words for the lesson but she taught me something special. I have always tried to fulfill expectations, and not everything expected of me is positive. The expectations started out as parental, then became my own. I spent years expecting myself to fail because I was unworthy of success.

The expectation for a kitten in a new house are as follows.

1. Existing cats will fight with the new one, no matter the age. The cats will fight for dominance. Kittens cause less of this but there will be yowling and fighting.

2. The kitten, like a new puppy, will spend the next two months crying for it’s mommy.

3. Kittens make messes, your new cat will probably poop on your bed, the floor, and miss the box a few times.

4. Kittens need constant attention.

5. Kittens will bite, tear, and claw.

Nymph has not met most of these expectations and the one she does, is not in the expected manner.

Truths about Nymph.

1. From her first moment in the door, she has been loving and gentle. She has not fought with Sprite except in the manner of play fighting. She has only cried out in pain when she is hurt because she ran into a wall or fell off of the couch and is hanging upside down and needs heroic rescuing. This has occured twice now, but she has mastered getting into the window.

2. Nymph does meow a lot, but her meow is musical and very sweet. She sounds a bit Siamese but without the added tones that I find unpleasant. She has the prettiest meow I have ever heard! Not once has she cried out of loneliness while I have been around. She has a few times called for me or Sprite, when disoriented or lost behind … the couch! She usually calls for us first thing when she wakes from sleep. If I speak she is quiet coming to sit on the floor by my chair. Sometimes she tries to get up here. She is quiet all night long.

3. The first day I had her I was holding her and she had to pee. I could feel her poor bladder stretched out. So i carried her to the litterbox, set her in and waited. She went, and hopped out. I did have Sprite teach her to cover her crap, because it hides the smell. She now over does that and will put it as low as she can. She has not once made a mess. She did vomit from eating too quickly a few days ago, but, that is different than the expected mess, and she has learned her limitations now. (She also REALLY likes Salmon).

4. I need more attention than Nymph it seems! Sprite has helped Nymph to get enough play, and I do play with this darling girl but she is okay if I ignore her. She does check in with me, and did about five minutes ago. She makes sure I am still around when she thinks I am too quiet, and I see more of her when I lay down. The chair is imposing and contributes, but each day she shows she is independent. She will play with the toys by herself, or she will play catch with Sprite. Catch is literal. Sprite flings a toy with her mouth, and Nymph returns it after pouncing it.

5. Nymph likes to claw things, but she prefers her scratching post and toys. She has scratched me once, though it was purely accidental. She is also teething so she wants to chew things to make her mouth feel better. She’s apparently swallowing the baby teeth that are falling out and has at times skipped the dry food even if this makes her hungrier for a day (I feed her extra wet food, because I am such a darned softy for this kitten) and every so often will go after my hands. She wants to nurse my pinkies. Still, all I have to do is say No, ouch. She has learned this means to stop and always feels bad. I get extra cuddling from her after.

This shows me two things. One thing I knew already, Sprite isn’t the only super amazing genuis cat ever born, and the other something I should have known and have at least figured out. Expectations are set before us, but not all of them are worthy of us.

People expect me to disappear when in public because of my disability. Today I punched someone, the third since my chair became a part of my life. Every time I go out people act like idiots and their expectation is that I enjoy inane questions, sometimes verbal and physical abuse, and I will just take it. Each time I have punched someone, I have found myself confused at the glee that others show. I do not expect glee at an act of physical violence. I often come to the conclusion that this reaction is because I did the unexpected and also I did something that these people desired for themselves.

Today a woman decided to poke me. I was waiting in line at Costco, my carer was in the restroom. She had been doing the potty dance, so I told her she should go because I could manage the transaction, my things were already unloaded. I asked her to stop nicely, I always try to be nice first. I am working on skipping the nice but I don’t think I can. She didn’t. I asked nicely twice, and snarled it. Upon being snarled at she put her face in mine. I held my breath incase she had eaten a cucumber and I punched her as hard as I could. I can punch hard but it hurts me too. My shoulder is aching and for two days my right arm will be of less use.

I never really know what to expect once I hit someone on one level, on another I expect for them to hit me back. No one has. The first person I knocked out, the second I don’t really remember today I just remember sore fingers, and the third ran off in tears. I think she called me names but I couldn’t understand her through the wailing.

The expectations of witnesses are to panic. No one has yet. Instead, people find my striking a bigot amusing. I get told variations of good job, I wish I could, and today a money saving coupon for money off of my purchase (I saved ten dollars!). I expect security. I expect reprimands. That has yet to happen. The cashier had been about to interviene, I realized this after I had hit her. She hadbeen speaking to the woman. I had already committed myself to feeling flesh on flesh and the spark of violence. I wasn’t angry. I was panicked.

I don’t hit out of anger. I expect it, when I am angry but the more I want to hit the less I let myself. I have yet to commit an act of violence with anger as an adult. As a child I did so mostly because I thought this was what was expected of someone when angry. I literally did not know better. I do now.

I know I could have taken care of the situation without hitting this woman yet, I feel GOOD about striking her. I knew immediately I was about to melt down if I didn’t contain the situation and put my headphones on, but I could keep one ear open. My carer missed the entire situation. I think the woman that I hit waited until she was gone before seeking to touch me. This means she was a predator. This means she was a threat. This is the time of year when I struggle most with violence, the fear of being hurt grows. This used to be the start of a half a year of self destruction followed by a half a year of recovery before I would be destroyed again. This cycle is ending.

I am fighting it. I was told I never could. I was told the expectations for me as an adult were not good.

Adult Expectations for Kat

1. You will never live on your own.
2. You will never work.
3. You will be in and out of institutions because you aren’t good enough for society (a therapist phrased it this way).
4. You will end up in jail.
5. You will commit suicide before you are 25. (This was before I was aware that I am supposed to die every year from my disabilities and illnesses.)
6. You will never get married.
7. You will be an abuser if you date.
8. No one can love you.
9. You are not strong, you can’t be independant.
10. You cannot take care of yourself.
11. You will always be lazy.
12. You are a hypochondriac, every time someone has a sickness you think you do too. This will lead you to self mutilation, and may be the cause of death that gets you before suicide. Not that it matters, because you aren’t a productive member of society.
13. You aren’t creative. No one will want you to be a writer, an artist, and you don’t sing as well as you think you do or you would be on the radio.

I list them this way, though I feel a few are redundant, because this was the list I was given when I turned 17. The therapist at the mental hospital I was in told me I was hopeless, that I would never make it to adulthood, muchless the twenty five mark. He made it clear that I was so valueless that there were no positive expectations for me. He said something that has haunted me more than his lack of respect. “If you were more like your older sister, then there would be hope.” He had never met H. He had only heard my mother’s biases. My sister was like the dead in a way, in that once she left she was treated as the saint that could do no wrong. Mind you, she ran off, got married to a close blood relative and had babies that she couldn’t take care of.

Yeah. She’s better than me in his eyes. I was angry. I believed him. I realized then and there that this was how the world saw me. He rehashed everything that my abusers had and would say. He took me down to nothingness, but as I was already as low as I could go he gave me something else. The first sensation of a spark of self respect.

This was not his intent. He was working on having me placed in a group home, because my mother agreed, I could never come home. After all, I was/am an evil horrible monster that will destroy family values and all that she cares about. Right? (Probably still am in her eyes… )

I behaved as he wanted. I learned how. I went to the Ranch, and I learned how to fake it in society. I learned the right facial expressions for the moods I have, according to other people. I don’t bother trying all that now, though a lot of that programming is still there. If I glower when happy, it’s because of pain. If I don’t act like a perky air head, it’s because I don’t feel like one. If I do not meet your expectations it’s because they are wrong.

The Truths About Kateryna Fury (Add Jackass in parenthesis to each statement. That’s what I feel when writing this part. Boy was that therapist an unqualified Jackass):
1. I live on my own. I have lived on my own as often as possible. I stopped living on my own once for financial reasons. I thrive on my own. I will never live with other people, unless it becomes state mandated, and then I will sue for my freedom.
2. Kateryna picks up her resume, skims it over and looks at the myriad of work that she has done. She notes her charity work, and with a smile that shows malice mails this off to the Jackass. (Novel Style Oh snap)
3. I am going to say this once. Needing the assistance of a therapist does not make you weak, it does not make you a person without value, and it does not mean that you are unworthy of society. If I need to go to an institution I will. I do not think I need this. Yes, I have mental health issues including depression and constant suicidal ideation (the words of the Jackass), I deal with PTSD. I learned the right way to handle this stuff… from therapists that are not jackasses. I have not set foot in an institution since becoming an adult, except once when I was hallucinating from pain and mistook this pain for psychosis, as I had yet to learn how to feel the difference. I was NOT admitted but instead had the doctors send me to the ER for medical reasons. I was given care and it wasn’t all in my head. I haven’t even found a therapist yet and have looked for the last year but I am not in the institution, nor will I go there. I’d die first because you work there.
4. Jail? Hmm… I do punch people. The only threat of Jail I have had was an illegal one. I do not break the laws, and the reasoning behind this statement was PTSD related. I hit people when I am afraid, and PTSD means for me constant fear. Finding a way to free myself from my PTSD and the link to my reactions in Autism set me free. I may go to jail someday in the future but I doubt it.
5. I turn 26 in September. So far I have not even tried to kill myself as an adult. I may want to at times but in reality that is internalized garbage from shit factories like you. In actuality a few of your patients have died, I know because we did know each other and it made the news. One was murdered, one was a suicide by cop (The patient you told me to idealize no less, though I mourn her you sure suck at your job, Jackass). Another overdosed on drugs. Me? I get my drugs the legal way. I follow my doctor’s orders. I do deal with my depression but I also know that when I want to die it’s pain. Pain people like you cause. Jackass.
6.I got married. I got unmarried. You were wrong, and your statement implies everyone should be married. So you wanted me to follow socially normative behavior instead of doing what is best for me. You wanted me to find someone who could put their penis in me, regardless of my sexuality. In fact you out and out told me I could not be a bisexual because bisexuality was an illness. I love all genders equally. All. Not two. All. I am Omnisexual, Jackass. Your white heterocisgender racist able bodied male privilege is showing. Jackass.
7. I figured out before you were done trying to make me give up on life, since that was your apparent goal and you had such high expectations for me and hopes for me that you were wrong and blind to much of reality. I knew this then, when I was so drugged up I couldn’t think and can barely remember much besides you and your hateful criminal actions. I understand, you presume that I should be like my sister who IS an abuser. This must be why you said this. You don’t believe in people breaking the cycle do you, Jackass? I will not be abused nor will I abuse. My first thought with each action is about consequence. For me. For them.
8. Jackass. (I believe that says enough). In case that wasn’t clear, I cannot count the people who love me and whom I love, because the number is infinite, as I cannot count that high. Jack. Ass.
9. I am the strongest person I know, and I know many strong people. I do know that sounds prideful yet, I can only assess others by my own knowledge and for me, I am the strongest. I think I have to be as well. My strength is not physical but mental, the very thing you thought I did not have. You drug me into a fog and decide I am stupid. That’s good medical care. Yes you have an MD and the whatever it is for psychology. Oooh. You are a Jackass anyway! Maybe even more so. Instead of paying attention to your patients you let me walk around with gangrene, you let me walk around with severe and deadly allergies, and a giant tumor in my intestine and buttocks. I did not cry or scream. Even the nurses commented on this when changing my bandages, I should’ve cried out more. Does strength mean crying out? Does it mean silence? For me it is both. For you? Obviously you are a jackass so what does YOUR opinion and expectation matter Dr.Jackass?
10. Hmm… I can too. I do all the time. In fact having a caregiver is a proof of this, as I had to advocate in order to get the need met. So my body wore out because I believed you… Jackass, you are again wrong. I can care for myself and I do with each breath.
11. Error, this is invalid. By not working myself to death I am lazy in the world of the Jackass. Therefore, I have never been lazy. Jackass.
12. Funny, everything you said was in my head wasn’t. Everything you said wasn’t real was. Someone is an unqualified Jackass! Or are you overqualified in your credentials for being a jackass? I get it. Therapy is, for you, about ignoring the body completely. I remember how angry you were when I had to have not one but two surgeries under the umbrella of your care, and… yes… I did survive and still have a crappy body. It turns out NOTHING was in my head in the realm of hypochondria and every disease that I thought I may have and wanted to ask my doctor about I do. Each time you coddled the other girl with Reynauds and made me suffer, that was wrong. Then again you told me that though I had signs of being Autistic I couldn’t because I am a girl. Hah. Sexist Jackass.
13. Well, this was added on just because it speaks for itself. I sing, I write music, I write audio plays, I write stories, and I write here. Someday you may read this, wondering if this was one of your patients. The answer is yes. If you are a therapist read this and pay attention. How much of this have you done to someone? Why give up on someone and tell them? This harmed me. No one will love me, everything I am passionate about is worthless, and… the most damaging thing a therapist can do is reiterate the words of an abuser.

This was the best therapist I had had up to that point. Each one tried to stick so many labels on me and not a one, even this jackass, saw me as a person. Each one only saw flaws. Some didn’t care about my not wanting God and others required it. I faked being a Christian until I was on my own as an adult. I did this in order to escape more abuse by THERAPISTS.

I also question a profession that’s name can be split into the rapist. I question a profession that tells the victim they must abuse. I question a profession that though it an be helpful can do so much damage. I question anyone that tells any person that there is no chance something is medical. I question why someone has expectations of me at all. I don’t think people should.

I will always strive to fall short of expectations. I know some are positive but for me expectation is obligation. If I succeed and am not expected to, there is anger. If I do not succeed and am expected to, there is anger. Expectation is also the measure of success. I have no expectations of myself, I merely focus on living and being happy. My happiness is more and more common.

I am still hunting for a therapist. One that can understand that therapy itself should have a trigger warning. One that does not victim blame, one that does not set expectations.

I don’t have a life goal right now, because life IS my goal. I will not work again, for a long time, because working would probably do me in. Why is this an instant assessment of a person’s value? Why must I fit in with your expectations?

I am glad Nymph opened this door. I wish it was free of the PTSD, but nothing I do can be free of that. Maybe someday, but not this one. This is also the reason why I have felt guilt for suggesting that someone finds a therapist. Yet, the good therapists are the ones who help people. It’s a shame they are so rare.

A Response to the Movie and Comic Book Kick Ass (Trigger Warning Based on Material)

Dear readers, this post and the aforementioned movie and comic book should all come with a trigger warning. I felt I should post this down here because I am going to try and write this with as few triggers as I can but Mark Millar seems to be one hell of an abusive person and therefore there is plenty of abuse to talk about.

I am an avid comic book reader. I like pretty much any comic you hand me. I’ve even managed to enjoy Archie comics. I did not enjoy Kick Ass. I read it because of the hype. I also borrowed it because of the hype. Hype usually means patriarchy. In this case it was formulaic patriarchy with racism, tons of homophobia, and of course as much child abuse as possible. That’s pretty much all Kick Ass is.

You see the writer, and I use that term loosely, creates (again a term used loosely) a world where superheroes kill everything as violently as they can. Wait what? It gets better. Super heroes kill everything that moves, and a father shoots his daughter repeatedly so she knows how it feels. Yes she has Kevlar. Does that make it any less triggering? NO. Does that make the training that Hit Girl endures to become someone that can kill with a smile less child abuse? No, it actually adds to it.

You see in reality I have had enough training that I could ostensibly have pulled off running around and killing people ala Hit Girl. Except that I didn’t want to kill people. Except that anyone that can kill with a smile has some serious psychological issues. Except that yeah my body sucks now and a huge component of that disabling pain comes from those same abuses. A child’s body will not handle the effects of being beaten in the same way as an adults. The damage is longer lasting.

So, right off in both the comic book and the film I was triggered. The film was in some ways less homophobic, and in many was more racist and anti woman. I realized as I watched Hit girl slaughtering a bunch of black men that Hit Girl is designed to reenforce the patriarchy. You see, if a woman has the power to kill you she will do it with a smile. She will lose her innocence (a lot of the blood shed metaphores of yore work out for this movie. Hit girl is rarely touched by males and is cold. Hard.) A woman that is capable of violence is instantly a killer. There are also elements of the madonna whore in a school girl outfit given. There were attempts made by Hitgirl to flirt. Yes, an eight year old or whatever she is was trying to flirt her way around.

Healthy imagery. In fact everything in this series is a carefully selected trope of what makes a man a man, what makes a woman great, and all of these are cliches. One of the worse changes between the comics and the movies was the reason that the big evil black man dies introducing Kick Ass to Hit Girl. In the comic book Kick Ass is going to save a stranger from domestic violence. (More triggers, and tons of racism). In the comic book the woman is black, the man is black. There is a part of this that is rare, as usually the black man is the predator after the young white girl. Of course there is also tons of racism since the man is a thug for the mafia and is apparently deserving of a katana through the chest…

Cue the movie. Any gaping void that was there in the isms was filled in. In the movie the high school girl that is with Kickass as his friend because he is supposedly a gay prostitute (she likes to save those poor people who aren’t with in the patriarchial boundaries you see) is now the victim. This is ahuge change of reason for both the characters. Kick Ass loses an element of heroism because he is just taking care of the girl he wants to have sex with. The black villain cliche o’ racism loses an element of being semi-original but still super duper racist because of course Hollywood cannot sell us something that isn’t made to reenforce the patriarchy so fully that I end up almost puking before the end of the film.

Mark Millar fans that see this as an attack, go ahead. It is. I am attacking his racism. I am attacking his homophobia. I am also attacking his comic book writing credentials. I can do better. Know how I know? I have WRITTEN COMIC BOOKS. If the villains kill less people than the heroes how are people supposed to identify with them? My issues with this film were so high I had to talk it out with a friend, and he had a great quote.

“the fight scenes which kind of sound cool…really bored me…there was no emotional reason behind the last hour of the film…yes her father was killed…but it almost didn’t feel like his death was truly acknowledged and rather it just went into super vengeance mode which no superhero should do. Where the hell was morality in all of this?”

You see, what makes a super hero heroic, as the movie Hancock tried to tell us between it’s cliches and tropes o racism and bad acting was that a hero will not be accepted by the world if they act with baseless violence. You may think so Mark Millar but you aren’t the world. I understand a great many people think this movie is great. Those people aren’t looking at this film and aren’t identifying which origins and characters you plagerised. Spiderman without powers, the Punisher, Batman/owlman/bluebeetle, oh and even your movie didn’t have a consistent soundtrack because the soundtrack was a mishmash of all previous heroing movie sound tracks. Could you BE more obvious with your movie,comic.videogame baiting cycle?

No. The answer is no.

There are people who like this film. The majority of people that like this film are stuck in the patriarchy unaware by choice of how baselessly ridiculous this film is. They have to work at it. You see, there isn’t anything original about Kickass. We’ve had better gore from Saw, we’ve had the same origin stories over and over. Except that the difference between Robin and Hit Girl lies in how they were trained. Yes Frank Miller tried to make Batman a violent abuser, but the public panned that and this was undone. Robin was trained carefully, so that he would know how to fight without killing. Hit Girl was trained to be an assassin without morals.

Kickass doesn’t. If anything the fight scenes are full of so many stupid choreographic moves that would get the characters killed, the set physics of that world are destroyed, and wait a rocket pack? Anyone that actually saw the film is probably wondering what Kickass coated his suit in so his butt didn’t catch on fire. This movie is not worth my share of the almighty dollar, the comic book s aren’t. In general, I don’t read or pay for anything with Mark Millar as the writer or creator. This will only continue until he learns how to write past a formulary, past the patriarchy, and with in the boundaries of what makes a Superhero SUPER.

Oh and if you have seizures, they use a strobe light in the film to try and make the fight scenes look cooler after they go video game baiting in one of the “climactic” scenes that felt so anticlimactic for those people I know.

So to recap, Movie bad. Mark Millarr is a hack. He hasn’t written anything I can think of that didn’t scream, “Hollywood, make me a movie because I am a pile of Cliche! Steaming RIGHT HERE!” This is just my opinion of course. An opinion I will back with my money and my mouth. Millar, if you want to ever have a write off let me know. Here’s your Corkscrew of Justice, you know where to shove it.

Shaming the Survivor (Trigger Warning and Foul Language Warning)

It is everywhere, the societal shaming of people. I could title this victim shaming or victim blaming yet, there is an aspect to being a survivor beyond the aspects of being a victim. The part of me that is a survivor identifies with John McClain, it wants to die hard if it has to die at all. The part of me that identifies as a victim couldn’t fight hard enough to survive. Same coin, two sides. When I advocate I must be a survivor, the victim aspect is too fragile to risk exposing to the shame.

You may have already run into this, at least once in your life. Something happens to you, and instead of being happy that you are alive, someone you know or must deal with reacts with disgust that you had to do things to survive, things that hurt you or went against the grain of society. The person that defends herself against a violent man and hurts him is not lauded but is feared by the patriarchy. Society moves to shame the survivors, keep it hidden away, don’t talk about it. This aspect leaks into other things. Surviving rape is immediately putting yourself at risk of being accused of deserving it. Rape can be deadly, therefore, to live you must have given in slightly, this is the myth. You asked for it and enjoyed it or you would be dead right? Wrong.

There is overlap with victim blaming yet, I haven’t come across a discussion about shaming the survivor. In a country/culture that has fat shame, thin shame, skin color shame, hair shame, race shame, gender shame, sex shame… it is hard pressed to find anything that is not seen as shameful. Other things are never acknowledged. Perhaps it is in that the feminists who are able bodied or did not endure domestic violence or… (insert qualifier here) cannot put it into ideas. Perhaps it is that these same women who attempt to speak for everyone with a vagina but only if they were born that way and are able bodied and white… do just that. They exclude. Before I was disabled I felt excluded because I  have survived. I felt shamed for having questions and not having picked up books on the subject. My nascent moment of identifying with the feminists died the moment one of them shamed me. I remember the words, the tone, and the sting. The woman was old enough to be my mother, she was blond, tall, and pretty. The topic was how to raise awareness about domestic violence, which resonated with me. I asked this question: “What if we pooled some money or raised funding via grants to open a shelter that gives access to women who aren’t married?” I hadn’t been homeless as an adult yet, I hadn’t known I would be in a sinking boat. I went further, the room had fallen silent so I stood up. In that moment I was appearing as able bodied, straight, white, and pretty by the societal standards. “Most of the shelters in our city cater only to those with children, and there needs to be a place for everyone.” That was what they were preaching. I thought the idea would be great. The response instead was as follows.

“Women like us never use shelters, we don’t need them, because we won’t ever lose our jobs or our families.” In that moment, the words said in this acid tongued manner that curdled by gut, I sat down and wondered why they called themselves feminists and why they bothered trying. I was excluded by class, my clothes were fashionable but I was not in the class I appeared to be. I was excluded by experience. Obviously the woman who spoke had never been in need, and in that moment I was cut adrift from feminism. I tried many times to reconnect but, despite some correct things and other incorrect things I did not belong in their puzzle. The ideals fit, but the people did not. There was discussion of how to further how to protect, but never the action that would help lower class (financially and educationally) women. Instead there was a pandering aspect to their own able bodied white privilege.

It hurt. It left me feeling so alone in the world. Months later I was further away from their ideal woman, deserving of help. I began to advocate alone. I have only worked with someone else during my advocacy rarely, because I do not want to be shamed for my experiences and I have yet to find true intersectionality. Sometimes my methods for getting my voice heard horrify people. To me there is nothing wrong with being a bit loud, or refusing to move when the police order me to as long as it is legal for me to do so. I am a rebel with many causes, and I see it everywhere I turn with the larger groups, if I do not fit their expectation of survivor there is shame.

Thankfully advocacy groups are rarely seen from this angle, I know I have the benefit of being a social chameleon, and that cuts down on people accusing me of things, assuming the wrong thing, or I just don’t admit what they do not need to know. I should say didn’t, as, in the last few years I have stopped hiding the parts of me they won’t like. I lost allies, but they weren’t true allies as a result.

I haven’t been shamed for surviving in a long time, but I had put distance between what I had survived and the moments I was living in. I see in my head snapshots of myself through the ages of my life, the phases, and the moments. They tumble down, twisting around each other before they burn up into a cloud of white smoke and I am still me. I let myself grow distant from them, focusing on living. Living became the act of surviving and once again I am being forced to justify my reason for not letting myself be murdered.

I realized that it was an attempt to shame me with the insurance. This week I had to justify the assessment for the wheelchair again. The woman on the phone asked me what I did to damage my body. “I had an abusive caregiver, I was starved and my first chair was damaged. It also never fit my needs or worked properly before that.”

“Uh huh, well did that caregiver beat you because abuse is just not reason enough for us to approve this chair.”

I wanted to scream, curse, cry, and shout. Instead I took a breath and said. “I was starved, are you aware of the ramifications on the body caused by starvation? I had less than 750 calories a day. My body consumed it’s strength to not die. My internal will to live also came into play, when I had to escape said abuser, I had to move. The replacement caregiver was also abusive, so I had to clean the entire apartment myself, I had to lift boxes, and I had to do this or I would have nothing left of my life with no way to replace it. I had to do this with a wheelchair that was broken.”

“So this is a self inflicted injury.” She started to go on and I let myself snarl.

“So you want your clients to just die when the options are injury that further disables them or death?”

She was quiet, I felt my anger and I let it be. I am working on that, as I fear anger. Anger usually means violence. I just felt it. It was about ten seconds, she was obviously thinking.

“No, it was just… you should have asked for help or something!”

It was my fault, in this woman’s mind. I have met her before, she is like the woman who shamed me for having an idea, like the reporter who didn’t understand that the ADA protects her too, and I had the click. Society wants survivors to stay silent, or to take the blame. It’s the same aspect, but in t his case the blame is the act of living itself. It is all tied like a spiderweb to the same isms, over and over again.

“I did, many times over. I begged, I pleaded.” I described the murder kit to her, I described my efforts of cleaning, lifting, dragging, crawling. Then, I turned it towards money. “So, now that you know all that, let me add something else into the mix. The chair will cost you less than the surgery and ER visits needed when I crack my head open because I lost my balance trying to do it your way, check my records I recently went to the ER. That costs you once about as much as the chair. That visit was preventable with treatment. You can approve me or deny me, I know others also have a say but if it comes down to my life being worth less to you than the cost of the chair, I will cost you more because I won’t die. I am a survivor. I plan to live a very long time, and as angry as you are that some disabled person gets help from your taxes… that’s just too damned bad.”

I was told it is too expensive. I was told over and over it is too expensive. My right to the freedom to move is too expensive. Even if it means I might die. I am hoping that my words left HER feeling shame, and anyone who hears the recording of that call. She and her company should be ashamed that my living is less important to them than profiting off of the illnesses of people. The capitalistic nature of my country has caused illness to be comodified. I am not a commodity item to the insurance company but I am to the wheelchair company and in a nursing home my name would be beds. I will now always be poor, but I refuse to be known as cost burden, potential profit or beds.

My name is Kateryna Fury. If you think it is wrong for me to have fought and dug and clawed my way out of abuse more times than I can count, fuck you. You heard me. I am breaking my own personal rules. It makes me edgy mentally to do so, a bit nutty feeling but FUCK YOU. FUCK YOU FOR THINKING THAT IT IS BAD FOR ME TO LIVE. When you break, because everyone does eventually in some way, someone will shame you for not dying. I hope you think for a moment and realize that you did the same over and over again.You are the cause of the term Survivor’s guilt. No one should ever feel guilty for living. EVER. Even bad people have a right to life, maybe you and your epic hatred of all things with a pulse made the person you think is bad act in that manner. Maybe it is all your fault you FUCKER. FUCK YOU.

My name is Kateryna Fury. I am glad to know that you also have survived, that you have fought and clawed and dug your way out of abuse, that you are a survivor. If you are in the act of surviving, then know you are not alone. I am proud of you. Your living has value not just to you but to me. It is so wonderful you want to live. As you recover, remember, you are loved.

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