Tracey Ullman Fail

So called comedians often use minorities for their humor. I never find this funny, and usually question why I bother trying to watch comedy shows after a certain point. Today I noticed the on-demand section for ShowTime had the “Tracey Ullman’s United States” section added. I started the first program, and right off the script starts with bashing illegal immigrants, Tracey Ullman, a white woman, in black face. It moves on to her mocking the Indian Culture, Islam, and Italians. She also mocks the very real medical ailment of Restless Leg Syndrome. It may sound funny, but, your legs burning all the time, unable to keep them still? Very problematic.

Instead of funny this show seems to show her hate. She makes fun of mostly ethnic groups, minorities, but makes fun of just enough white people to get away with her bigotry by the standards of those blind to their privilege. She makes fun of those from the south. She makes fun of everyone.

Hold up a mirror Tracey. Hold up a mirror to yourself and see just how sad you are. She goes with victim blaming, rape jokes, and does she see what this does to people? This isn’t funny. It is aggressively disgusting.

This may be old news, but, maybe someone will read this and will take notice. It is never funny to demean someone. It is never appropriate to put on black face. That was never funny. Ever. It is not appropriate to have your Indian Woman character sing her sentences in a mock Bollywood production while her life is threatened. It isn’t funny to play out acts of Xenophobia.

This show was supposed to be about America. Why then does any non white person have a thick accent that is usually unintelligible? Racism. Bigotry. Crap.

Not only is this show anti female, it is anti human. I will never watch another Tracey Ullman special. I can’t stand the stench of her tastelessness.

I am sure somewhere online you can find justifications for how she creates her characters to mock bigots. If the effect is more mocking of the minority, you have fail.

I felt this after one episode, I am trying a second.

More black face. More racial cliches. Showing a woman of color as toothless, uneducated, and irresponsible is NOT Funny. Mocking the Veterans of the Iraq war? Wrong. We need to support our soldiers even if we do not support the War itself. These individuals signed up with the intent to protect us.

Making fun of erectile dysfunction I can let pass, but wait… for many non elderly men Viagra has been an aid in achieving some of life’s more pleasurable aspects. It can help the disabled male perform, which can be psychologically freeing. Stating that elderly men who use Viagra will use it to sleep with whores is disrespectful to both sex workers and the elderly. Who has the right to judge the partner of another? Not me. Not you. Not Tracey Ullman.

Making fun of Poverty is inappropriate. Saying that a kid is “Shit at Math” is inappropriate. It doesn’t matter if parents say this all the time, a kid will believe it and will stop trying. It is important to encourage children, way to reinforce negatives.

Making fun of hard working individuals, those who have disabilities, making fun of those who are more naive about the world at large. None of this is funny. Doing this two episodes in a row? Mocking religion, not okay. No matter what religion it is. No matter how controversial you want to be, being a bigot is just not funny.

There is plenty of comedy without oppressing people. When the “funniest” stuff you do is antihuman, which this crap is… you are failing. When the non racist bits aren’t funny how do you get called a comedian?

I therefore give the elusive and rare Corkscrew of Justice to Tracey Ullman. You. FAIL.

Beauty

I am tired of the stereotype of beauty. I grew up being told that a girl should like men who look like Brad Pitt. I like women with soft lush curves, big and strong ones too. Many would consider my past conquests masculine, or overly thin, or fat. No one type fits what I like. I too have “strange” preferences for the men I have dated and these too tend towards those with meat on their bones, they have body hair, they are dark skinned, fair skinned, or really just alive.

Most of them, but not all, are tall. With either sex I tend to reach out for the taller people, though tall has changed in meaning since the wheelchair entered my life. I can’t look up at my baby brother without hurting my neck. He sits down for me, and still towers above. He is about seven feet tall. I love height because my family is full of tall people, except my own biological father. I associate height with safety. What does this mean about the other standards of beauty? Are we all programmed to like certain things?

Yes!

A huge part of my persecution in this life has been based on facets of my physical appearance. I have red hair, very pale skin that burns the instant sun touches it, soft full lips, and I have always had curves. My smallest size is a fourteen. I was barely eating to maintain that. My body needs meat on it. I am simply a curvaceous woman. I do have an ample bosom as well, and all of these things have been picked at.

I grew up being told I should be blonde. Blonde meant perfection. I hardly find blondes attractive as a result. I am aware that most of my siblings and my own mother are all blonde, and this factors in too. I think Blue Eyes are the best, though any shade is lovely to me. Blue eyes were mocked, because they are pale. Being a minority as a white person is very rare in any part of the world, the patriarchal structure still dominates and is usually white, even in countries where white is the minority. I have always been told my pale skin makes me wealthy. Whiteness in my state is a status symbol.

In India women who are by nature in the darker end of the spectrum are considered harder to marry off, they have less value based on something as simple as their genetic make up. The lighter you are, the more respect you can gain. This is White Privilege. It has defaced an entire culture, this love of all things white has poisoned us. You see whiteness in media, dominantly with able bodied super muscular WHITE men. You see their blonde perfection everywhere. I think back to the Nazi Propaganda studies group I was a member of in High School, and that is what I see. Reflections of past propaganda, continued, accepted, and fully realized.

Curly hair is considered disheveled. Girls with curly hair wake up at odd hours to iron their hair out. I think it is lovely, and my standard of beauty includes the use of a curling iron to add curls to my hair. This is rare, the era of the Super Perm died out at the end of the Eighties, except for a few hold outs.

I am told I must wear make up to seem presentable. I do, at times like to wear make up but I do it when it feels good. Usually I will also hide some of my facial scars under make up, if I cannot shake my feelings of Paranoia. I do not allow myself to wear make up on days when my self worth is being questioned, or when my confidence would hinge only on sultry red lips.

As I write this I am watching a movie that has what I consider the equivalent of Black Face. Sophia Loren is the Millionairess, Peter Sellers is the Indian Doctor who teaches her how to be more than a spoiled snob. This movie is full of propaganda that is anti woman, anti persons of color. I was enjoying it until I realized the fallacy that a white man is playing an Indian, with hardly any alteration of skin color and a very cliched accent.

I also note that the famed figure of Sophia Lauren seems to be aided via a corset. I might be wrong, but the extremes to her figure seem to need assistance. It doesn’t feel natural to me, though it does fit the “standard of beauty”. Her hair is lightened a bit, and of course she is always shown in posh and polished appeal during this film.

I do not think Brad Pitt is handsome. I think he is mediocre. This is all about looks, not his acting. I will not malign someone for having a career. I will however state that I do not understand the requirement to find him attractive. If you want to know who I find attractive in Hollywood, you will have to dig deep. There are few people that strike me as gorgeous or stunning, especially since we have entered the Anorexia Age of Hollyweird. Health is beautiful. That inner glow of self acceptance can make anyone gorgeous.

Since my blossoming into awareness about privilege I have seen more beauty in the world. This side effect shocked me. I like to compliment people when I find them attractive, and I have had the urge to tell the entire world how beautiful it is. The beauty I see is nothing like what is in the Movies or on Television. I live in a world of diversity. The people I see daily are of mixed race, from other countries, and their voices alone are a rhythmic song.

I am not beautiful by the overly BMI oriented modern sensibilities. I never will be. I’d have to break my bones, cut my body apart, inject myself with dye, and lose my sense of self. (This statement does not mean that those who naturally fit this standard are not beautiful, it is merely a rejection of the expectation to alter myself to be just like them) I reject the need to starve myself to fit a rare body type. I reject the fashion industry’s expectation that “fat” women do not like Fashion. I LOVE clothes shopping, and am discovering that I could easily spend a million dollars on cute shoes. These are cliches about womanhood, and yet you will find I only have four pairs of shoes, two for winter, two for summer. My clothing is all rather sensible, black, and boring.

I am pigeon holed by my lack of thinness. I am trapped by the need for others to stigmatize those who are not identical to them. I am not a Stepford Cripple, I am not anything but a person. I am flesh, I am bone, and I have soul. You are beautiful. My friend who is an immigrant is beautiful. I love listening to her voice, the way that she sings while she speaks entrances me. My friend who is the son of immigrants is beautiful. He cannot see that because his world is full of hatred, hatred of the Other.

I discuss privilege with my friends. It is an unavoidable conversation now. Eventually it is addressed either by discussion of politics, feminism, or simply the venting of frustration. I no longer hide my beliefs, to survive until the next day. I am free to speak them. Most of the time these conversations hold a similar impact, someone learns something. We all do really. My friends are all shapes and sizes. I have friends who are thin, blonde, and blue eyed. I have friends who are extraordinarily fat, but give hugs that are so soft. I have friends of every shape, size, mental capacity, and ability. My friends are all beautiful. You are beautiful.

Stop stigmatizing people for not being clones. Clones are scary, according to the media pundits and science fiction. Every time the word cloning is mentioned on TV it is with the hush of fear. Disability also has that hush of fear. Stop being afraid. Fear stops you from living life. This doesn’t mean you should ignore some fears, such as the fear of hunger or the fear of a snake bite. Stop fearing things that are different. If you do not understand something, educate yourself. Don’t fear it. Don’t shun it.

This includes fine art, not so fine art, but most especially people. Children are people. Women are people. I see often abuse launched at those who are different. I experience it every time I go out. I was reminded however, of the power of kindness and decorum.

I write often about the importance of gentle resistance, passive resistance, and not striking back. I admit I fail this way at times but, every so often I am given the reminder I need, the proof that I am right. I had transferred out of my chair at Sam’s Club, into the van and rolled down the window. Beside me a harried mother of two beautiful children, her disabled mother, and a cart of groceries struggled. I watched in silence, until they were about to leave, calling out to the woman that her mother had forgotten her cane.

Her son looked up as she thanked me, glad to not have to spend another twenty five dollars on a cane, and said, “Mommy, that’s the lady from the Walmart with the kitty!” His mother paused and said, “She was on TV too.” We talked then, and I complimented her for handling the stress. I could see she was frazzled, and I let her kids talk to Sprite while she settled them in. No petting of course, but, I told her how beautiful her family is. Three words. “You have a beautiful family.” Okay, five. I never was good with numbers.

She froze, looked at her kids, and then smiled. “I wish everyone could see that.” The thing I have not mentioned is this. Her children are Triracial. They are of Asian, African, and Caucasian Descent. I wanted to take them home with me, their sweetness gave me a rare pang of desire for Motherhood. It went away before we were out of the parking lot, but not the reminder that everything you do has a lasting impression. Every word, Every laugh, Every shout, every time you teach someone something. There is impact.

What draws me to people is never what they look like. It is instead their personality, the joy they have for life, and sometimes the hope that I can grow up to be like them. I may never grow up. I am always surprised when I realize for a moment I am not a child anymore. It fades, but, that too reminds me to be innocent.

Beauty is not in the eye of the beholder. It is not what media tells us it should be. Beauty is merely in the existence of life. Flowers, Puppies, kittens, children, lovers. All beautiful. Be you a Homosexual, Transgendered, A person of non Caucasian ethnicity, red haired, blonde haired, black haired, green haired, or even a strange shade of orange. You are beautiful.

Beyond the Search Words

I normally name my posts before I type them out, it helps me to retain focus. Instead, I am unable to hammer out a decent title, or one free of curse words anyway. I decided, in my insomnia fit, to peruse the offerings of the internet with a few search words. Disabled and handicapped being the top two. I wanted to see what came up. I am not linking any of the blogs I found, because beyond what is already in my blogroll or private reading list (waiting for me to put it in the blogroll) disgusts me.

Ignoring the posts about disabled porn, ignoring the jokes at the expense of handicapped people I came across what appeared to be a journal of a trip by a handicapped woman. A cold and a broken leg are difficult but not disabilities, are they? The cold isn’t a disability but reasonably the leg could be a temporary disability. Not only does it effect your daily function but even after the bone heals there can be lingering damage. I still had a visceral reaction to the writing, and not in a good way.

I understand disability, and the challenges inherent in trying to maneuver in spaces that are cramped, dealing with prejudice, but writing an entire blog about how you broke your leg and that instantly makes you the most disabled person in the world is really not something I can get behind. Yes, I admit that the writer’s pain is important. However, so is their dignity.

It took me a long time to find out how to blog, because of that very thing. I did not understand the point of blogging, I did not understand that it could be done with Dignity. It was the need for dignity that lead me to posting that very first time, and each time it is the basis for my editing, rejection of some of the writing and my attempts to be open minded.

I strive for personal dignity and I work hard to not strip away the dignity of others. Reading about how cruel the world is for those with an obviously broken leg, the desire for pity instead of dignity frustrated me. So I moved on, another person was complaining about handicapped parking, and how rude it is for people who are handicapped to use it. I read about this one a lot, it sneaks up in most blogs at some point. The concept that a safe spot, with enough room to move a ramp out, your chair, and easier access to a building is beyond some people.

Moving on again, I had to do some deep breathing, refusing to let myself post cutting words to try and make them see. Attacking people, no matter how much I disagree with them is not something I want to do. That would lack grace on my part and could remove their dignity. Then, I found another post laying out another problem people seem to have with handicapped parking.

Did you know that “all handicapped drivers park crookedly, blocking me out of my car when I park near those damned cripples”? Not only is this a blanket statement making it a stereotype but, I often have to have our van pulled out, because there is rarely handicapped parking, and the cars by able bodied people are often parked just as poorly. I am not a driver, so I am not aware of how hard it is to parallel park, but with the monster chair that does not turn I cannot do it in a conference room. I perceive this act as massively difficult.

I am often tempted by magnetic signs that say “Please do not block access to this door, a ramp is contained inside and access is needed for my wheelchair”. I do not because of the local culture. It might qualify as a subculture, and yet it is dominant in my daily life. The culture towards the disabled springs from a lot of superstition and the very poor education available.

I know that the education offered to the American Children fails more and more annually, yet if you are slightly different or have any challenges you are shoved into a room and no one wants to see you. No one teaches you. I am primarily self educated, except for the teachers who actually cared enough to break into my world.

Being aware of this, and what was taught about disability in school, I know that they fear me. the ubiquitous they, in this case means the average New Mexican. The little that was taught about disability in my schooling included first, that disabled people could never function in society unless they were Franklin Delano Roosevelt, though we were taught he contracted Polio after his presidency. This is a fallacy, as I know now. Then, we were taught too, that no disabled person ever did anything of historical value. Disabled people are just evil. The contradiction in FDR’s existence never seemed to make a difference.

The superstitions continue, one of the local superstitions states that if a pregnant woman sees a horror or a disabled person, her child will be disfigured in the womb. This means if you are pregnant and stare too long at a person in a chair or even a person with a broken leg, you kill your baby. A lot of the pregnant women out here are teenagers, and a lot of the pregnant women teens and adults drink and smoke. yet the blame falls to the disabled.

The more I read tonight the more frustrated I grow. I did stop, but only to protect myself from festering rage. A cold is not a disability. Illness does not mean disability. A broken leg is a physical injury but injury does not always mean disability. Depending on the rate you heal, you might need a placard, temporarily, but that does not mean you quantifiable understand what it is to be truly disabled. Your pain is valid, do not use it to invalidate mine.

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.

Isms, Hisms and Hersms

I read a few blogs on the internet circuit, some of them deal with feminism, some deal with racism, some deal with ableism, and others deal with Fatism. Isms of all shapes, sizes, colors, and one for each of us, sometimes two. Someone was having a sale on their isms when our culture was created, tossing them out like sprinkles on a cake. I am tired of isms today.

I have a great doctor. I will recommend her to just about anyone, for in her office there are no isms, just lists of things to get done. I now have an epipen, a referral for the dozens of undiagnosed whats its, and even a new diagnosis. I also was given the option of advocating for breast cancer awareness. The point was made that with my body being as it is, I have become acutely aware of risks and am in the perfect position to teach other disabled women about breast cancer.

I have thankfully never had breast cancer or even felt a strange lump but I do self exams weekly. I know it is recommended that you do monthly examinations, yet, this is not enough for me. I have relatives who have had cancer in all of their parts. Breast, brain, uterine, ovarian, liver, lung, you name it, and it has had cancer. I also have a lot of conditions, including one that effects my skin and therefore hypervigilance is necessary. Beyond this, what has made my doctor decide I am a great advocate? Self adaptation.

My breasts weigh a lot. Not only is the tissue very dense, making them pert and perky despite their size, but, it makes it harder to find lumps once you breach the FF quadrant. I left that a long time ago. I shared with her today my methods for a successful self examination. I have to adapt to the needs of my body and this means I may lay on my side, I may hang upside down, but, I always make certain to feel not just my breasts in a circular and consistent fashion, but my armpits and down my sides a bit.

I am lucky that I have had strong women in my life. I have an aunt who has had stage four Breast Cancer for longer than I have been alive. This woman has fought, and fought and thrives. She does at times worry her family for her life, but, she has dealt with cancer with no break for over twenty five years. In my mind she is the best teacher I can have about why cancer awareness is so important. Without knowing her, I might not have decided to live during one of the bouts with suicidal thoughts that I went through as a teenager. I might not have begun to battle with myself for proper medical care.

I have a lot of diagnosis, the list grows daily, but, my isms are mine. I am a short, fat, white girl in a wheelchair. I am also blessed with very rare breasts, the sort that women have painful surgery to mirror. I have great hair, great eyes (when they see) and a brain. I am facing daily challenges with ableism, fatism, and even some fetishism. Sexism is a consistent battle. I also face the blessings of people who are better than the isms. I face the knowledge given to me by my fellow females, and now I must learn to share.

Take stock of your isms, be you male or female. Take a look at what you are given by station in life, what you have fought for, and, if you have enough to share, reach out and help someone rise above. I will post about my chances to advocate for breast health. I am even going to start getting mammograms, a need I had hoped to put off for at least ten more years, but perhaps I can come up with a way to make them less painful.

This is hardly a new idea, I am merely following in the path of others who have taught me. This is not an area I had ever expected to be asked to advocate in, but, how can I deny the request when I know that even one person may become self aware?

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