Bruises

I have multiple conditions that require that I bruise easily, and I always feel bruised after slight bumps but it isn’t until weeks after the injury that I start to show bruising.

In my early life I thought this was a good thing. It meant that my father’s abuses wouldn’t show and therefore I was a better child. This was directly reflecting the attitudes in my home. In fact my lack of bruising often caused my family to ignore the seriousness of some of my injuries, which has lead me to my current state of disability.

I have wondered often in my life on many topics from “Is Nicolai Tesla Autistic?” on through, “Why does Sylvani try and nurse milk but can drink water?” This is one of the topics I have mulled over the longest. My doctor’s offered no explanations, which at first disconcerted me. We are raised in the US to believe that our doctor’s are all knowing and the ones who behave like Gregory House are the ultimate in doctors.

This prevents people from asking questions, this makes it harder for a disabled person or a person with a yet to be diagnosed chronic illness to be taken seriously. If said person has a vagina and breasts on their person they are going to have to fight to have the slightest ailment taken care of muchless a more serious issue. I became highly aware of this when I started self diagnosing.

Self diagnosing is a huge no no, as this gets one labelled a hypochondriac, even if the questions are meant in an innocent fashion. In my case it was little moments where I met someone with a disorder, such as Reynaud’s the circulatory condition. My case is actually worse than this person’s and as I asked her questions about her disorder and found I had literally every symptom I began to worry. She was nice about it and we both believed I had the same condition. It helped that I would turn blue faster when it was cold or when I was stressed.

The adults ignored the physical symptoms and decided I was somatizing. So I learned to keep my mouth shut and stay away from doctors. I thought for a long time my mother was absolutely right about the medical world. At times I wonder if her experiences with medicine and their misdiagnosis are why she doesn’t go to a doctor, but I feel more certain that it is because an abuser also wants their victims kept away from medicine. This is a part of why people die from abuse so readily. If you cannot get a doctor and have internal bleeding, you are screwed.

Over the years I have never once had an answer for why I bruise so slowly. This has inhibited my ability to know if i am injured in areas where I am numb if the skin is not split, sometimes the skin splits don’t show for a while as well. For example when I was injured on the paratransit. It took me almost a week to figure out that I really was hurt. This was between my spinal cord injury, slow bruising, and the signals from my brain putting the pain in my right leg between my hip or my knee when the wound was touched. I couldn’t find anything in the area my brain TOLD me was hurt.

I am thinking on the life long ramifications of my body’s build. I know, at least I hypothesis, why I don’t bruise like someone with Ehlers-Danlos usually does. Not only because no two humans with the same medical illnesses are identical, even identical twins have interior differences, but a confluence of small veins and low circulation has kept me from being black and blue.

Every blood draw I have had I am faced with a phlebotamist’s lament about the smallness of my veins. Every time I have to convince a doctor that I have EDS, I must point out the fact that not every patient has the significant bruising and though I feel my bruises they don’t always show. It isn’t the excuse given before about deep tissue bruising. Not every bruise is going to be in my muscles, and those hurt in a whole different way. No, my lack of bruising is a lack of blood flow to the injury.

I started thinking on this yesterday as I woke up from my nap and my face resembled a chipmunk. The dislocations were atrocious yesterday, so my face shows the marks still. Perhaps I bruise less because my blood is busy swelling up my head, or my hands, or anywhere but where I expect too.

I can go back to my next task. Between halloween preparations I have been watching every James Bond movie that has been produced, all 22 of them. This is a painful excercise yet it has a purpose. I decided to find out the evolution of the Bond Girl. I remember loathing Halley Berry’s portrayal and being uncertain as to why, so I decided to investigate. I am not liking my findings. I suspect some people may deem them controversial!

Also a reminder: I am not planning to write during October. October is my runaround like a chicken partying month, so I shall resume my current scampering.

Afterburn (Trigger Warning)

I have had my pain meds for almost a week. I still can feel the after image of the pain, it’s tracking me like some sort of monster. In my mind there is a shadow, and if I look behind there feels a chance to see the negative image of my being drawn out by the pain. The monster is created by the black hole of pain, that inescapable pain that takes lives. In every motion I make there is the risk that I will hurt like that again. The fear is enough to make me hesitate. This is the after burn. This is the concequence.

It comes up when I want to do something such as spending money for a keyboard that isn’t broken, or saving for a computer that isn’t dying a slow and icky death. My keyboard has had a short in the usb wire for a good while. I found out about it during my time with the Paintrocity. I don’t use wireless keyboards for two reasons, batteries and also I tend to break those a lot faster. This keyboard has actually lasted for years and through several computers, it is a veteran in my typo wars. It’s been packed away for moves from the first time I lived on my own through this permanent time.

This keyboard has been dropped, run over by the scooter, and I wonder if objects feel each time I “hurt” it. Never on purpose because it is a life line. Perhaps it is this attachment that makes me hesitate but I think not. I think it is just having the pain again. The last time I felt this way was not the last time that my meds were removed from my life. With that I was already feeling pain and things were different due to abuse. That was another type of pain, even though it included bodily anguish and mental anguish. There is no comparison. This is NOT the worst pain of my life. It is merely the current pain.

Afterburn pain doesn’t go away with a pill. I know a large part of it is mental, some of it is a symptom of lost ability from having to stay still so that I didn’t give in to the urge to just scream. Some of it is rebuilding the barrier between my pain and my brain. I don’t know if this is a bad thing or not. I think with the new wheels it is giving me a bit of perspective on what my body benefits most from about the chair. That would definately be the adjustability of my body without my having to twist and shift. So far I have had a dramatic relief in all pain except my lower back where the actual spinal injury is. That pain won’t go away ever, I learned this a long time ago.

Still, with the Paintrocity I am afraid to explore. I am almost using my too narrow gate as an excuse. Almost. I fear more not having my shiny new wheels and if I force through the gate I may damage the controller wire or something else, therefore I have to be patient and wait for the manager to take the gate off it’s hinges, remove two blocks of wood and reattach it on the other side so that it swings fully open and doesn’t murder my rose bush. I have beautiful yellow roses in bloom.

The Paintrocity has me afraid to do anything. Eating? No. Why? It will make me digest and digestion hurt so badly without the medication. Breathing? I still catch myself starting to hold my breath because the injury in my back effects my diaphragm. Singing? I won’t let myself stop but that puts my lower back into a form of torture. The singing brings up more mental challenges with this. Even laying in bed is unpleasant now. It now reminds me of being trapped in my home.

I am going to call the manager today and let him know I need the gate fixed by Friday. Rather short notice occured but I have a graduation to attend, and I want to be there. Parts of me are afraid. This would be my first time in a huge crowd with these wheels but, these wheels have immaculate control, they turn in tight spaces, and oh yeah, I am taller. The seat of this chair is about four inches higher, then if I tilt it back I feel like some sort of six foot tall seated person.

The after burn has a very visceral image in my mind. It belongs in a horror movie. I become a negative image. It is my own reverse flash come to destroy my life, to devalue everything I love. The paintrocity even tried to remove my ability to hold Sprite. Yesterday was the first time since the pain meds return when we could truly lay together for naptime and both be comfortable. She had her head on my shoulder, so whenever I would shift a bit or wake up and opened my eyes I could see her curled up against me, using me as a pillow fast asleep. The adorableness helped dispell some of my fear of sleeping.

I think that was the worst part of the latest experience with no shelter from my pain. I did not go through what I thought of as withdrawals but instead into spirals of deeper pain. Sleep became a place of more nightmare than not. For a long time the only nightmares I had were related to the murder that I witnessed. Even in the pain those went away because I spoke up. The dreams consisted mostly of my parents relaying how much they cared for me. That is a very bad thing with parents like mine. The paintrocity also made me more vulnerable to talking with anyone who is a “leech”. I have a few in my life. I only answered the phone for one once.

Even as I write this I am left with a quaking feeling in my gut. My mother admitted she reads my blog. Well during my time of pain when I wanted to kill myself I wrote a letter detailing all of the things that made me angry about wanting to die. I understood still and reminded myself that the pain was escapable if I trusted my service coordinator and advocate. I just had to wait a little longer. Just a little more time. Those words were torture. I just wanted to slit my wrists. I considered eating some of the non pain medications en masse to see if I would die. I considered dragging myself to the street. The plan ended there because that was NOT happening. I had to talk myself out of it, and I found myself angry at wanting to die. I found myself angrier that the voice in my head telling me to die sounded like my mother or my father always. It was never my internal voice.

Some of the things I wrote I will never write about here, some I will. I determined long ago that this is my blog, this is my space, and my parents are far from good but they are also far from the only abusive parents in the world. For my entire life I have thought of my mother as a victim. That stopped. This was a benefit of the paintrocity. Anyone that could let their children be abused and excuses it as it was better for them than being without a father, or lets them take the beating so that they don’t have to IS an abuser. She may not have dirtied her hands as often as Steve (that’s my biological cretin of a father’s name by the way) but she still did abuse. There were words, moments, and even a few times she hit me because she didn’t like what I was feeling. I don’t know that I can forgive her for what she has done. I don’t know that I will ever visit the family again. My baby sister is old enough now that she is a fully formed adult. If she needs me she can call. I don’t have to endure an abusive grandmother, an abusie mother, and her worst drug dealer ever husband

I finally understand why after calling her or her calling me I feel so horrible. She’s like her mother. I don’t know if she will read this post but I will never say those words outloud to  her. Every time she told me I was just like my father it cut to the soul. The paintrocity helped me to relive those moments.

I still have a lack of good color to my skin, I still have these dark blue circles under my eyes. I always have them when I don’t feel quite right. The darker and bigger those circles the worse the pain is. I felt for a while during the pain that my face had vanished under them. Both my caregivers were concerned more than once about how grey I had become. I looked like a zombie. I was a zombie lost to the pain. They made me eat. They made me drink. I did not want to. This was something I asked of them in preparation and both caregivers worked with me admirably. There were days when I just growled at them. They still worked, they still did all that we needed. There was nothing that either did that made pain worse either. That is a challenge.

My face has always betrayed how much I hurt. When I saw it happening in the mirror or it was commented on I felt naked, and I expected pain in the form of abuse or manipulation. Every other time someone else has added to those burdens. I trust that in the moments when everything melted into PTSD land or I was hallucenating very bad things that neither did anything wrong. If they were going to they would do it regardless of coherency. My experience with abusers has also told me they would want me to remember, so that I would know that they had power over me. Disconcerting? Absolutely.

I know eventually I will defeat my formless foe, the Paintrocity. I will get back to where I feel almost carefree. I have never quite managed carefree, but I have come close. Now that I have mobility restored I may attain actual carefree during some moments. I have goals, I have dreams, and I have begun to live already. Like a thirsting plant that just needed water. Sprite has taken to the chair as well. In less than a day she stopped hiding for most of my jaunts around the living room for food or water. She didn’t like going outside on the leash but after that she started jumping up onto my lap, she found out she can’t sit on my headrest and she’s sitting on the table waiting for me to finish typing.

My pain is lessened further because I cut my hair off. I am now short hair bearer. I like the style, and it looks good one me. (No style I have ever had has been out and out bad except the time I shaved my head.) It feels good. I am sending the grocery bag full of hair (and I do mean full, I was apparently very hairy) to the people gathering hair for the Oil Spills. Because the hair is dyed it was not appropriate for Locks of Love but now I know there is another charity that can use my hair for good.

I do not yet know what it will take to beat the Paintrocity except for living. I do know that I do not fear dying anymore. I don’t think I qualify as suicidal. Part of this is that I had reached my goal of not wanting to kill myself daily before my pain meds were denied by the insurance, and I managed to make it until the last four days before I wanted to die. Even when I wanted to I could use the truth over the pain induced self hate and lies in order to not give up or in. I had been living all along. That sensation of waiting to live that was torture is at an end.

Now I just need my corset and I have it all.

Selling the Magic Cure for Pain!

Right now, there are dozens of ads airing on a handful of stations in your area, perhaps every single one, schilling pain drugs. I tend to change the channel when these magic pills are advertised. Nothing cures pain, it just blocks the signals to the brain. “My Fibromyalgia pain has hampered my life, until I found this pill and became an above average American with no pain who can do it all, this pill turns you into Super cripple and has a musical name to boot! Try Elyricembril today.”

The expectation that these commercials set is unrealistic. I used to hold out hope that a pain pill would come along and take the ache out of my joints, or a pill would make it where my joints would stop dislocating. Tonight, I moved my pillow two inches and dislocated my right shoulder. Right then, a Lyrica commercial came on. I couldn’t change the channel, and saw a bunch of white privilege added in to boot. Not only is this woman schilling a drug, but, her family is all happy, has everything they need despite her invisible illness. There is no suffering all because of their magic little pill. This woman is blonde, thin, and has no needs beyond their pill.

The reality is so different. All these commercials do is add to the sense of defeat that a person with a disability faces. Those who are the hardest hit have no diagnosis, their bodies just fail. They do not get the luxury of knowing why. My list of medical labels is a luxury, I do take it for granted, but it is worse for those with no labels, no treatment, and often no job or home.

A part of me yearns for socialized medicine, with our government understanding the need for medical care for everyone. This would mean my caregiver would not have to ignore those aches and pains he feels daily, that to me indicate that there is likely a problem. As the depression that we are in, it is not a recession that is merely denial by wealthy men who fear the truth, gets worse so increases the amount of untreated medical ailments. Some include the diagnosed but many are ignoring small injuries tearing themselves apart and whispering in their minds, “When this recession ends, I’ll get a magic pill.”

There is no magic pill. There is nothing that takes away the pain. There is nothing that can cure you if you get sick enough. Sometimes you are just born sick. You do deserve medical care, but, turn off the commercials. The medicine that works best for many is not new, but is older medication ignored until nothing sold on TV, written on a pen, or advertised to doctors who are often paid to give out these pills works. There is no magic pill. There is no Truth in Advertising.

I might sound bitter, as I lay here writing. I feel pain in my body with every breath. I know there is no cure. There is no end for my pain. It has gotten worse through my life, each day it gets worse. I have tried everything, and usually once this is revealed my doctors give up. I have not given up. I am far from bitter. I am merely growling at a threat. The threat that kills hope, the threat that removes treatment, and the threat that further disables the mind. There is no magic pill.

If you are reading this, feeling alone, and need support. There is that. Not only are there support groups everywhere, but, you can contact me via my blog either in the form of a comment or using the contact form and I will talk with you. Friendship is free, and is often the best thing for those in pain. You aren’t alone. There may be no magic pill, but, that does not mean there is no hope. If you are reading this and have been feeling the ache of frustration, anger, or sorrow knowing someone else may see these advertisements and feel false hope then the crash that comes after, reach out. After all, if we save ourselves, support ourselves, or merely even convince a doctor to try something old, we win. There are many ways to lose, and the magic pill is one of them.

Medicalization of Humanity

I have spent my life being a patient. Most people do to an extent but a lot of non disabled people do not wind up in a doctor’s office monthly. Those that do are usually seeing a psychologist. I have been talking to my biological mother again, because she needs my help. In exchange for helping her with training her dog to be a Service Dog I asked for payment in therapy. Not literally, but, figuratively.

I think she was startled but, I am wounded emotionally. I am so angry at her, and I need to forgive her. I can’t do that without working out some of the issues and I want a mother. Some of the things that have angered me include over medicalization of my emotions. Being human has never been an option for me, despite the obvious inability to escape it.

From reading my blog you know already I have a history of abuse and chronic illness. You might have also noted an undercurrent of loathing for labels, though I am working to embrace mine. Some labels cannot be avoided. After becoming an adult I went and paid for a psychoanalyst to evaluate me. I wanted to know if, without my mother’s influencing them with her fears, I was really as insane as everyone told me.

I did this because I didn’t feel crazy. I felt depressed, but, not crazy. I did not think I was becoming a sociopath like my father. I put effort into fighting that, and won. What I did, to help prevent influence in this doctor’s office by my past was withhold information. It took several calls to find a doctor willing to work with zero patient history, but, the woman who did the test with me understood my need to find the truth.

In my childhood I was diagnosed with Borderline Personality Disorder, Bipolar, Depression, and a slew of other labels that never quite fit, including Multiple Personality Disorder. Most of these get renamed with each DSM, and with number V coming out (I don’t know my roman numerals and I am not looking up the translation, it is either four or five), I am again feeling pensive.

Part of it is the sudden ability to cry. For the first 23 and a half years of my life I could not cry without bleeding. I cannot seem to suppress my tears anymore. Again, some of this is because of effort though the effort sends me receding into myself at times. With that test, I was freed from the stigma of most of the labels I had received.

Those that stuck are depression, lower case because it is something that is perfectly natural considering my family history and personal history. It also is not something I will ever treat with pills again. Another is obsessive compulsive disorder. I need the world to be in order, and this comes from my past. Anything out of place could cause a beating. My disability has helped me with this. I cannot order the world, and I am healing because of it. I had no way of cleaning my room for years, it was horrible.

The test also helped hint at something else, I am Autistic. I have Aspergers. I haven’t told many people, just my Person and my mother. Now the world knows. I feared the Stigma of Autism. My best friend (All my friends are my best friends) Maxis is autistic and helped me to realize that my Autism just lets me be me. It has made things more difficult in some ways but I have adapted, and am extremely high functioning and no one can tell. My labels are not readily visible.

I also am an adult with Attention Deficit Disorder. I adapted as a child, after taking Ritalin. The Ritalin made what turns out to be a side effect of the autism, my extreme sound sensitivity, worse. I couldn’t stop screaming, all my pain was there, and of course I turned out to be allergic to it. My mother pulled me off of the drug despite my institutionalization. I recollect hearing her voice through a closed door, I was curled up in a corner in the Time Out room, being punished for not brushing my hair. My mother had come to visit and I had cried telling her how loud everything was, and hearing her tell the staff off for drugging me was the best sound out of all of them.

I am still sound sensitive. I can hear the sounds most people tune out. When a computer is turned on, each second I hear the scraping of the needle in the hard drive. it is deafening. I have five running right now, and have adapted to the cacophony of my world by adding more stimulus. I have yet to find true silence, even with a power outage but that is the best peace ever. Still, having mental distractions helps me cope.

I find it a bit ironic that being nearly deaf in one ear has not decreased my ability to be overstimulated by sound. Overloading is so far what works best. The great part about hearing everything is hearing my cats purr, when no one else can. Sometimes that sound is the best in the world. My nerves have always been just as sensitive, my skin feels too much and that can cause even the touch of William’s paw to have me crying out.

Still, in my life more damage has been done by mental health practitioners. I have been supposed to find a therapist for almost a year. First, I used the excuse of insurance, which did not cover without a copay. Then when that was fixed, I used the excuse of truth. I do not want a Therapist. I really hate them, and do not trust them. I am aware of my need now, to find one. I need someone to work with, so that I can help myself and my mother.

I remember my first Therapist. Her name was Candy, and my father upon finding this out asked if my Mother was taking us to see a stripper. He thought it was funny, I thought it meant that the doctor tore up paper. Instead, she told my mother that she could change my father. She told me and my sister, we all shared the sessions, how women must learn to cook and my bruises and burns, were just the signs that I was going to be a great wife.

I never believed her. My sister did, and when I told her at night that I thought that Candy was insane, she told me that she is a doctor, so therefore I must be wrong. I kept it to myself but at the age of four I just told her things I thought she wanted to hear. My father was sent to a mental hospital after attacking a man, or something like that a year later, and my mother did not let him back in, despite Candy telling her we would all go to hell. I think the woman let her religious tenancies effect her job.

The next therapist I saw was the one who had me put on my first Antidepressant. I was almost eight, and Doctor Baca decided I was depressed. Likely he was right but he never let me address why. He wasn’t a listener but talked about how I needed to try harder in school, how I needed to bathe more, how I needed to do things to be popular. If I got a word in edgewise he used it to shame me. I had begun to develop breasts, and upon relating the nickname I had at school, because my bra broke in Phys Ed, he agreed. I was slut shamed. The Nickname is not related here as it reveals the name that I have shed, but it contained the word whore.

The list of bad therapists goes on and on. No person is perfect but even the best amid them just wanted to label me. Many tried dangerous tactics and all of them post Doctor Baca insisted on medications. I took so many pills, and many had adverse effects including causing me to gain 100lbs in a month, but, the pills were more important than the girl. Each doctor took any crying as a sign not of emotional release but of depression. If I was happy at all it was a manic, if I was angry it meant I was psychotic. I lost touch with emotion itself.

My response was to try and kill myself, though, I couldn’t figure out how and asked my mother to help. The first time wasn’t the cause of my institutionalization, though the threat was leveled. I just didn’t comprehend it. The suicidal ideation passed and yet my brain warred to follow the rules that were leveled at it. My needs were far from met, and my Autism being undiagnosed meant I had no help. I was adrift, and lost.

The worst weekend of my childhood came then. I was beaten to the point of nearly dying, and denied medical treatment. There is much more to that story but it will not be blogged about, my fear of being attacked over it is too strong. My entire life was changed at that moment however. That is the hinge of life for me. That too, is when my personality changed the first time. The direct result of head trauma. That is the weekend where the first breaks in my back were had, my Xrays showing as an adult that when I was about eight I had four vertebrae break in my back, two in my neck. They healed well enough thankfully but I was in agony, I was alone, and I knew that I should not trust anyone ever again.

I was also threatened with food. My father had decided I was fat. I wasn’t yet, I was perfectly healthy, but he decided I should stop eating. He also instructed me to cut myself, though I did not manage that one. I did manage the eating disorder. He had told me too, if I did eat he would know and would beat my mother to death. I had to protect her. She always has needed my protection. So I gave up food. It was not hard, due to the pain.

Pain is the best appetite suppressant I know of. It kills the urge to eat in me, and is the reason for many people becoming malnourished with access to food. I lied to my mother the first few days and told her I wasn’t hungry, but, then she told me my refusal to eat hurt her. If I didn’t eat she’d surely die. Catch 22. No matter my choice she would die. I decided to eat, then, I would just throw up after dinner. Then my “daddy” couldn’t kill her and she wouldn’t know so she wouldn’t die.

This worked for a while, and my stomach stopped hurting and my skin even healed from some of it’s symptoms of allergy. I was however, bulimic by the diagnostic standard. No one asked why I was bulimic at the tender age of eight. My family didn’t figure it out very quickly, but, eventually they did. I am sure I had a decline in health. My memory was very foggy, and I had begun to have bursts of rage. Perhaps this came from the head injury, the painful seizures that I had started to have, hiding everything, or the burden of the household falling to an eight year old girl. It could even be the bulimia, the overdosing of drugs by my doctors, or, all of the untreated genetic ailments.

My stepfather had begun molesting my older sister, he was too afraid of me to hurt me, so I shaved my head. We discovered then how misshapen my skull is. My skin had begun to split on my breasts, and I thought if I was a boy then I would always be safe. I was of course unaware of the stigmas that were to come, but, I thought being male would make it all better. So, I tried to cut my breasts off. I failed, and for that I am grateful now. I am not sure what the therapists told my mother about all of this, but, from my perspective no one took into account that something might be wrong physically or that the abuse took a toll.

I was taken to a hospital, dumped off, and my mind and body were invaded. I do not know why these doctors thought a physical examination was necessary my first night there, but, they gave me a complete physical, including a pap smear. There was no explanation, but, I lashed out. My first night there was spent in the padded room of solitary confinement.

Diagnosis were tossed at me like darts at a board, seeing if one could fit close enough. Most of the girls there were suicidal, all of them had been molested or raped. Each of them had been battered, and all of the children were in pain. The staff were not all kind. One of the male staff would hit me, but I never said a word. He told me if I did, he’d see to it that I did not get to see my mother ever again.

My hair is also complex. Only half of it is curly, and this is all in the under hair. I had to bathe twice a day there to pass their cleanliness challenge, because of the Hidradenitis Suppertiva causing excessive sweat. I was allergic to the shampoo and cried each time I bathed. They gave me more antidepressants.

I mentioned once, how much my body hurt to the doctors there. I was quickly learning though, that all they wanted was for me to suddenly become a normal child. I wasn’t sure what that meant but noted what the children who got to go home endured. They could not yell, they could not scream, they ate every meal but not seconds, and they were nice all the time, if the adults were looking. I began to master the system. This meant no crying, so I got even better at being a machine. I let my world fall into their system of order.

I did go home, but, I couldn’t keep up the act of perfection. So, the cycle hit over and over again. I still couldn’t eat but was gaining weight. I was shamed for it. I was stuck then in either my mother’s clothes or sweat pants. Time passed and I was a teenager. My first period came on the eve of another hospitalization. I thought I was dying. The inability for people to discuss this function without clinical talk or shame had cost me knowing that this was going to happen. It didn’t help that my mother had told me all about how evil my Uncle Verne is. Verne is a rapist, a pedophile, and of course he would surely be out to get my mother’s children.

She had me stay with my grandmother while she made arrangements to have her crazy and devalued daughter locked away. My uncle called. Grandma had left me alone, despite my mother’s very valid fear that I would kill myself. I was considering it staring into her medicine cabinet when the phone rang. This was before caller ID hit that small town. I thought it was my mother. I thought maybe she had realized that the kids at school were mean, my hands hurt, and so did my stomach and I just couldn’t live like that. It was a strange voice. His voice was raspy, cold, and hearing me he sounded suddenly excited. I talked with him for a while, until I realized who he was. We didn’t trade names but when he called me by mine, I asked if he was my uncle.

There it was again, that duality, I was told by my mother that upon pain being dealt my way, I must never be rude on the phone. I was also told I must never let my uncle know where we were, who we were or to hurt me. I was terrified. Then, I felt warmth running down my legs. I remember what I said, “I am sorry Mr. Uncle Verne, I have to go now. I will tell my Grandma you called.” I hung up and went and sat in the tub crying because I was bleeding.

I thought that I was going to die, which, saved me from my suicidal thoughts. It was partly there because so often I was asked if I wanted to die. The idea wasn’t original to me, though I may have wound up having it anyway. I am not blaming the doctors, as without them I still would have died, I am merely questioning their methods. For every emotion there was a label, a drug, and a punishment.

For my fear of my period I was told I was a misogynist. I hadn’t even known what that was, but, upon being told I hate women, I thought it apt. At that time I wasn’t aware that self hatred is not the same, and the over labeling and medicalization was helping me to dehumanize. I was instead a child trying to make people love me. At this time my memories of my Sensei had been suppressed, and yet the mark of them remained, I was subconsciously seeking that same love.

The rest if my timeline, up until the Ranch, mentioned in earlier posts, is a blur, a mix of self hatred, cruelty, and a few bright moments when I went off the medication without telling people. Not all of my memories were destroyed by the meds, and the medicine did help me learn to control my flashbacks. I was so lonely however, unable to make contact with myself, isolated, and then something amazing happened. My freshman year of Highschool, I became the Valentines Princess. In my school this was on par with the popularity contests of Home Coming Queen or Princess and Prom Queen. My classmates elected me, and openly made this truth known, because of the simple fact that the most popular girl in school was pregnant and did not know who the father was. The pregnancy was not the issue, many other girls were pregnant too, it was the culture of this town. If you were not sexually active you were not acceptable. It was that she had cheated. Perhaps it was a form of slut shaming, but I was only aware of the fact that I had won. I had been chosen to represent the beauty of my class, a symbol of the perfection of love.

These memories are so crisp, as is the memory of my sudden happiness ending, realizing I had to tell my mother that I had won and needed a dress. There was no way I could take the title. I went to tell the coordinator, another student in my class and she found me first. She had already talked to the other wealthy students, and they were going to pool their allowances to buy me a dress, a trip to the salon to style my hair and they were going to have my hair done. They also were going to give me a free ticket to the Dance. At this point, my mother had left my Step Father, and money was so tight we could barely afford food. When I told her however, I expected anger and was given joy. She was happy for me.

We went through the rituals of beauty, I even shaved my legs, ignoring the pain that caused. We had my hair done, and, when I walked out with my Tiara in place, taking the arm of the boy I thought was the most handsome in school, ignoring his displeasure at being my escort, I stared out at the people in my school and was given a moment of joy. No one booed. I had expected that, after all every day I was on the outside. I kept the roses the principle bought each of the Valentines Court members for years, only shedding them when I no longer needed the reminder of my value, for I am worth more than roses and a popularity contest.

When I told my therapist about the feelings I had had, he told me I was becoming a narcissist. He berated me for every single feeling, and I went back on the meds. I was so certain he was right, and that my mother was too. The messages given to me during these visits to the psychologist were all so negative. Tomorrow I am calling and making appointments again. I am an adult now, perhaps, this will free me from some of the pain I feel. Perhaps I will find one who is willing to work with me on how to emotionally survive my physical pain. If I am offered medication my first visit, I will not return to that doctor.

I am still fighting for my humanity. I grew up meeting and failing expectations, never making my own. I am an adult now, and my own expectations are met. Yet when I cry, even at the end of a sad movie, I question, evaluate, and judge myself. My crying is the hardest, it is the most difficult for me to allow. I have come to embrace Happiness, anger, jealousy, but sorrow is the biggest terror. Even in the media we face the words of stigma. Pharmaceutical companies, doctors ignoring the validity of emotion, deranged fathers, and depressed mothers (Feel free to rearrange, relabel, or adjust these two for your own needs) all collude against humanity.

This is not the only way that people are dehumanized just one example of it. There is something in the air, something in the water, or perhaps just a tradition diluted with time that has caused dehumanization to become far too common. Civil Rights are torn away from people based on their supposed inhumanity, the disabled are not granted access because we surely aren’t human. I tried so very hard to shed my humanity, yet without it I cannot sing, I cannot write, and I cannot breathe.

I am afraid of psychologists. What if they refuse to not try and force me to take drugs? What if it turns out in the future I was wrong and needed the antidepressants? The consequences of these choices are the real fear. I fear too, that my next psychologist will refuse to see my pain as real. The wheelchair is not enough for some people, or it is too much. I will be writing a how to article on shopping for psychologists, after I am done, detailing my method. I will share it here.

A Response to “What are Service Animals?”

This conversation was held on MSN. My friend is using the Alias Tiffy, in respect to her cat. She asked the question about service animals and our discussion illuminates a bit more about what a cat is capable of. Eventually I will (hopefully) post video of my cat performing her tasks. I am sad to say my cat has an Upper Respiratory Infection courtesy of the shelter system and our new housemate. This doesn’t mean that you should not adopt, just make sure to get your cats medical care when they need it. All typos are left as is in the conversation, though emoticons were removed.

Tiffy says:
Ah, makes sense but scince I can’t see you, how can a cat help you walk?
Kateryna says:
My cat naturally shifts her weight to not fall. So, I trained her to shift her weight to help me not fall. What this means is that when I am walking and start to tip too far in one direction she goes to the other side of me and I can compensate.
Kateryna says:
She has cut my falling down by over 90%
Kateryna says:
Not enough   To stop me needing a wheelchair but I can go pee without falling five times in the six step journey
Tiffy says:
I think I understand
Kateryna says:
Awesome
Kateryna says:
Any other questions?
Tiffy says:
What else is she trained to help with?
Kateryna says:
She alerts me when I forget to take my meds. There is thankfully a lag time between the morphine leaving my system and the pain slamming back into me, and she can sense it. The trained response is for her to either get my med bag for me, or to yowl three times in a row.
Kateryna says:
If I need my meds and cannot reach them she is also trained to retrieve them.
Kateryna says:
She can also dial for an ambulence and can even call Locke on his cell if I fall or somesuch
Tiffy says:
Wow
Kateryna says:
She is trained to warn me when someone approaches from behind me, which cuts down on flashbacks and/or protects me from a random hand right on the injury
Kateryna says:
She used to do more but she is aging and has been sick enough times that the training had to be forgotten for her own sake.
Kateryna says:
Her mouth got torn up, she used to pick up objects etc.
Kateryna says:
She is even trained to “read” some packaging for me at the store, because i am blind as a bat and cannot see much anymore. So, she identifies the shapes or however she does it and paws the package
Tiffy says:
Ow
Kateryna says:
Yeah, she is allergic to poultry and the reaction cut up he rmouth,
Kateryna says:
The other things she does are more instinctual responses with trained reactions
Tiffy says:
Poor thing =/
Kateryna says:
She has a particularly shrill warble she gives when I am going to pass out, and if I stay still she calms down
Kateryna says:
If i am going to have a seizure she will yowl until I either stop doing what I am doing, it hits, or until I sit down, depending on what I am up to.
Kateryna says:
during the pass out time she calls for help, by going to every room in the house and making a ruckus
Kateryna says:
When it is a seizure she moves up to my chest and sits there unless I signal her to get help
Tiffy says:
So I guess most people who have service animals are pretty attacted to them, they’re really amazing
Kateryna says:
she is too sick to work right now, and I cannot get out of bed.
Kateryna says:
Direct correlation.
Kateryna says:
Without my service animal I cannot go outside, I cannot function.
Kateryna says:
It is worse actually than what it was like before she came into my life, because although my back is broken and my legs barely work, with her I feel as free as I did before my injury, and in some ways freer.
Kateryna says:
I lack saftey, I lack security, I fell four times this morning trying to do my daily things like peeing, because she is sleeping off her sickness.
Kateryna says:
I am also terribly worried about her, so I am not as efficient in my work.
Kateryna says:
A service animal is another limb. I love her more than Locke, but he understands why.
Tiffy says:
I hope she gets better soon
Kateryna says:
When she was electrocuted a year ago, he sent me money we needed for him to move out here, it took another six months to get him here but she would[ve died without it, and i am not sure I could survive without them BOTH. One I can handle being without but it sucks.

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