301: Manwife Needed

(Warning: There is adult language in this post that some may find offensive.)

    And while you are at it, there is a c—– (insert vulgarity beeps) that needs cleaning…. This is how I wanted to end this post. But I found it overly offensive. So I put it in the front of the post, in order to confuse you more, and in hopes you might forget about it by the time you maneuver through the Nyquil mess below. I’m not calling my husband this time to check if it’s too inappropriate. I figure if people read Shades of some color or another, they can handle a bit of Crotch.

    I am writing because I need help. The house is a mess. I need a housecleaner. And no offense, but I’d much rather stare at a man doing my dishes than a female.

    I’ve been guilting myself up lately, as in telling myself those negative messages such as: I’m a lousy housekeeper, I hate cooking, I’m clumsy, I’m lazy, and I must be losing my fricken mind, as I can’t remember a darn thing.

    It’s a good thing God (or that purple-green alien guy) birthed me with a sense of humor. I’m the type of person who turns on the oven, and when the oven timer goes off, I wonder what the noise is. Worse, is, I’ll start to cook a meal, and then soon afterwards smell something yummy, and think to myself: What is that smell and where is it coming from? A while back I was yapping on my cellular phone, the palm of my hand pressing the phone into my ear, and then suddenly I panicked and starting searching the house, as I wondered where I last left my cellular phone.

    It’s ridiculous. I’m ridiculous. And I’ve decided I need help.

    I am a danger in the kitchen. I’ll start to boil soup, leave the room, and forget until the upstairs is filled with smoke. I come dangerously close to losing a finger every time I meet up with a knife, and following a recipe is like reading a very difficult language—like Japanese converted into brail and then into sign-language. I have to reread, and reread, and recheck, and then double check. Still, I usually mess up on some portion. Unless it’s just: add eggs and milk and stir. Then I forget where to look on the fridge shelf, or leave the fridge door open, or break the measuring glass, or if I get distracted before I begin cooking, I forget all together I preheated the oven and wonder why there is a mixing bowl on the counter. Or I get distracted by memories of the recent documentaries describing cage free hens that really aren’t cage free and the cruel treatment of cows and wonder if indeed the eggs are cage free and if the milk is happy milk, and not some milk tainted in cow sorrow.

    Sometimes I think there is something terribly wrong with me or that I am going senile; until I realize I’ve been this forgetful my whole life, and haven’t progressed in weirdness, just perhaps recognition of said peculiarity.

    I am so forgetful, and my short term memory is so lacking, that even grasping the spelling of a word that describes much of my condition (dyspraxia) is merely impossible to remember. Of course that critter of trouble, lovely dyslexia, doesn’t add to my ability to spell.

    It wasn’t until I was in college that a professor actually took the time to tell me to think in patterns and visual images when attempting to memorize spelling. She noticed my high-intelligence and thought it didn’t match my atrocious spelling. (You know what I love about Google? I can type in a wrong word and find the right word! I just typed: How do you spell atroshish. And voila, now I know; at least for ten more seconds I do.) My professor said to look at the word separate and notice the letter r was separated by two letter a’s. From then on I could spell separate.

    Since my spelling is already naturally atroshish, I kind of wish I messed up on easy words, too. Just for the phone of it. (< not intended to spell that way; total mistake.)

    I’d like to regularly misspell the word as as ass and but as butt. But I can already spell little words correctly. I guess that is what texting is for: a place where a but can be a butt and an as an ass. Is that redundant? Oh, the freedom. Only text-ville and Kindergarten classrooms have an excuse to misspell.

    Which reminds me…My husband used to squeeze my son’s naked butt cheeks together, and make the cheeks move like a mouth talking, (all our sons actually) and say, “Let me asssssk you a question.” And HE has never undergone psychic evaluation. Makes you wonder, doesn’t it?

    This is part of the reason, the butt jokes, that my eldest son is certain he was born into the wrong family; that and the fact that he is confident beyond measure, secure, a social butterfly, and life comes easy to him.

    He is what seer told me is called “Earth Bound.” I am not. I am “Mars Bound.” The planet, not the chocolate candy. Though now that I think about it, anything is possible.

    Now as I’m trying to force out of my mind the image of Mars bars looking like alien turds, I am squeezing my brain super hard trying to remember what I was laughing about earlier that had to do with a conversation with my oldest. The labor of thinking. Or the constipation of thinking. They are about the same.

    This isn’t what I was trying to remember, but this thought is first in line. So I will share:

    When I was delivering my eldest son, the labor and delivery team told me I was really good at pushing.

    My response: “I know; I’ve been constipated my whole life, so this is quite easy.”

    I’m just now remembering this; and thinking this might have been an aspie moment.

    Now I can remember.

    The conversation with my eldest yesterday went something like this:

    “Mom, you and Dad should get drunk once in a while. I never see you drink.”

    “We drink son, just in small amounts. I was actually tipsy the other night, because I had two glasses of wine.”

    “You need to loosen up, go have some drinks with Dad and come home drunk.”

    “Son, I have been tipsy before, you just don’t see it, as you don’t spend a lot of time hanging around with us when we have a drink or two.”

    “No, Mom, you need to get drunk like Dave’s dad did the other night. He was fun!”

    “What? Your friend’s dad got drunk while you were there?” Eyes shift sideways and eyebrow springs up.

    “Oh, Mom, just a little. I wish you and Dad were more like that. His dad was so funny when he was talking to us.”

    “Okay, let me get this straight: You want me to get drunk and hang out with your friends?”

    Son’s face blushes red. “No way! Yuck. That’s not what I’m saying at all.”

    “Yes it is!” Huge smile. “That’s exactly what you just said.”

    Silence, and then I’m pretty sure: FEAR.

    ~~~~~~~~~
    I woke up this morning still laughing at the conclusion of our drinking conversation. I was still in a playful mood, as I sat on the couch at noon and teased my son.

    “Thanks for giving me your cold, again. Chills followed by fever and body aches and sore throat, right?”

    Big smiling, fifteen-year-old says: “Yep. That’s it exactly. Tomorrow expect a runny nose. And you’ll sweat a lot at night. Oh, and you won’t be comfortable in your clothes.”

    “Well. If you see me running around the house naked, you know why.”

    Yes, this is how I communicate with my NT (neurotypical) son. We tease and joke, and laugh at life a lot. It’s how we connect. He gets me that way, and I get him.

    Sometimes though, I think he sucked all the social-skills out of me and middle son. Although, I often tease him, my Leo-star, that it is my fault he has so much confidence. When he was sound asleep, I used to sit at the edge of his bed every night and whisper: “You are handsome. You are smart. You are loved.” I read somewhere in a book about subliminal messages, and assuring my eldest’s self-esteem kind of became a little bit of an obsession.

    I wish someone would lean into my ear at night, and whisper sweetness. Depending on my mood, I think if someone is already whispering, they are saying this: You are endowed with supernatural healing powers and your natural, nutrient-giving fuel is chocolate. Dark if available. But any will do.

    I think it gets lost in translation though, shifted by unforgiving dyslexia into emboweled. Thusly the Mars Candybar Turd visions.

    I can’t even remember the focus of this post as I had a nighttime Nyquil in the daytime. This is my life. I do things backwards to survive. Nyquil gives me insomnia, just as non-drowsy Claritin makes me sleepy. I’ve learned not to trust lables.

    I know I wanted to talk about the need for a manwife, and that at the start of the post I was upset that no such word as manwife exists. It ought to be a word, women’s movement and all. Earlier, I was taken aback into a parade of delight as I made up new compound words with wife, such as casstlewife, trailer wife, tentwife, Yurkwife, motorhomewife, couchwife. I think the last one suits me. Now if I can use my magical mind powers to convince the rest of the world of the worthiness of couchness.

    Couchness reminds me of what we sometimes call my dog. Are you following my train of thought still? I used to call my miniature labradoodle Violet, after the character in A Series of Unfortunate Events, then I transitioned her to Spastic Colon, as she is a hyper-spastic dog and I suffered with IBS for years, and the name suited her and my journey in life. But in the late summer, I noticed after a week of no bath she has this awful smell. I really can’t stand it. It’s a female smell of some sort, and just plain nasty. So as a result, of her doggy stench, I started, in secret and in a soft silly voice, calling her Crotch. Well the name kind of stuck and caught on. So if you are at our house and you hear someone say: Hello, Spastic Colon or Come Here Crotch. Don’t get the wrong impression. We’re still a PG-13 rated house. We just call our dog after private parts.

    Originally, a hundred-thoughts ago, I was motivated to write this post based on an article on dyspraxia that a friend Sarah Sparkle of our support group shared. http://www.dyspraxiafoundation.org.uk/services/ad_symptoms.php

    I remembered reading about dyspraxia at the start of my blogging journey, last spring, and recognizing myself and my son clearly in the symptoms. And I thought, today, as I was reminded of our struggles, I ought to send the article to my husband. Mainly because he will be home soon and our kitchen looks like a giant hamster turned the area into its habitat.

    Also I want to remind him of why I can’t remember simple things, like the name of a movie I am watching. The review of the article describing aspects of dyspraxia really got me thinking that I do need a manwife; preferably foreign and dark, or from China. As an aside, I’ve been oddly attracted to Chinese foreign films lately, and fallen in love with some of the leading characters. Yes, I know it is make believe, but this is my current fixation. So flow with me on this one. Next week my manwife will be from Spain.

    I can picture him, the man I pay, in tight jeans and topless. I know it’s freezing here, and that most of the morning I had on a wool hat and the heat lamp singing my face, but this manwife is endowed with super powers; he is extremely self-motivated, energetic, and warm-blooded. And he’s not afraid of the camera, so I can post photos on Facebook and this blog, and you can drool. Unless you are a hetero-sexual man… then I can. Pause. Delete. I had typed some reference to my dog again. Enough of that already.

    Okay, so back to the focus of this post, which is basically: See How Goofy Sam is on Nyquil and somewhere layered beneath the challenges of dyspraxia.

    Dear Husband,

    The reasons I need a Manwife, based on dyspraxia:

    I can’t balance well, have a clumsy gait, and have poor hand-eye coordination. You totally know I drop things all the time! I have extreme difficulty standing for a long time and this challenge makes it hard to cook or do the dishes (and clean toilets). Also, I have difficulty starting actions and cleaning is a definite action. Therefore, logically, I have difficulty cleaning. This is basic logic. I have a tendency to bump into things. You know this. You see the bruises. The more I have to clean, the more chances I have of bumping into objects, and the more chances of booboos. I have difficulty using knifes. Remember when I sliced my finger? Remember how you look at me whenever I have a knife in my hand? Plus the website I linked above specifically lists difficulty with: “cutlery, cleaning, cooking, ironing.” That pretty much covers housework. I have tracking difficulty and this means I lose my place when reading. This makes recipes super hard to follow. I am over-sensitive to light; it’s good we live in gloomy skied Washington, but we do have those skylights and fluorescent fixtures in our kitchen. I am over-sensitive to noise, too. So the sound of the vacuum and even the fridge, while doing its humming thing, hurts my ears. I am also sensitive to smell, which makes cooking difficult. I am sensitive to temperature; this makes cooking over a hot stove gruesome. I have a poor sense of direction. Our house is big. I could get lost. I exhibit difficulty in planning and arranging my thoughts, which has nothing to do with cleaning, but is quite accurately displayed as one of my hidden talents in this post. I forget things. I could burn your shirt while ironing, if I ever took up ironing. And of course, since this pretty much describe me: “Slow to finish a task. May daydream and wander about aimlessly,” I think you should consider I am inept entirely at focusing on something that does not motivate me. I tend to get stressed and anxious easily, and housework triggers these things in me. No one ever told me how boys pee. And frankly, the mis-aiming thing…too much to handle.

    Sincerely,
    Your Wife

    (In all seriousness dyspraxia is a difficult condition to live with. I find it interesting how many traits of ASD and dyspraxia overlap.)

    If you are wondering how I will pay for the manwife, I’ve taken up a collection. Just Google Manwife for Sam or if you are a man put on this apron when you get home, take off your shirt, and get moving.

    _________________________________________

    * I did just call my husband and read him the first paragraph. He okayed it. So if you are offended, blame him.

    ** thank you to my friend Sarah Sparkle for sharing the article on dyspraxia with me today

    *** Sometimes this is my sense of humor.

300: Aspergers: The Stuff That Ain’t Working

1. Exposure Therapy:

For years and years I thought if I just socialized more, if I just connected more, and tried harder to be like everyone else, my endurance level for social gatherings would improve and my anxiety levels would decrease. I believed that through repeated exposure that things would get better. That hasn’t happened.

I don’t have a fear and/or phobia to any one thing or event; therefore there is nothing I can focus on overcoming or having less fear about. My anxiety isn’t caused by anything I can pinpoint. My anxiety is caused by the way I process the stimuli in my environment and the way I respond to my surroundings. I am hyper-aware and my senses are turned up to the highest degree. I am also, despite self-training and studies, unsure of how to act in a social gathering, (e.g, how much to share, when to share, when to stop, when to respond, how to stand, how to look, when to be less honest, etc.); and as a result of my uncertainty, I have a constant inner voice reminding me of how to be. A voice that also self-corrects continually.

I need and long for structure and routine. My fear can be reduced if the same events happen in a similar way. However, inevitably changes occur. To say I will get better with practice or exposure is not an accurate statement. First of all, I am not wrong or in need of improvement. I am uniquely wired. One would not tell a person with a visual impairment that if she kept staring at a picture on the wall the image would become clearer, and one would not tell a person with a hearing impairment to repeatedly listen to a song on high-volume to improve his or her hearing. In the same line of thinking, one cannot tell me to continue going outside of my comfort-zone, to eventually gain a sense of security. I do not have the physical capacity. This is not biologically possible for me.

2. Positive Self-Talk/Cognitive Therapy:

While Aspergers can, and often does, have the comorbid conditions of generalized anxiety disorder, OCD, and depression, Aspergers is not the sum of its parts. A person cannot be treated for the comorbid conditions and then grow out of Aspergers. If anyone says they outgrew Aspergers or cured themselves, I don’t believe they had ASD to begin with. Unless they’ve feasibly learned how to reprogram their brain.

I do not think there is a way to change my brain. And as hard as my life can be at times, I don’t like the idea of my brain changing. Aspergers is not a mental illness. The “disorder” of Aspergers is believed to occur in the frontal lobe of the brain. Why and how the condition develops is still largely unknown. Though there seems to be a large genetic factor.

While positive self-talk has many benefits and can decrease episodes of anxiety and depression, and perhaps even diminish some OCD tendencies, it does little to help with the condition of Aspergers itself. No matter how much self-talk I give myself, I still respond in a fight or flight response pattern, when I am in a public place or at a public gathering. I do not want to feel this way, and do not choose to feel this way, but this is the way I feel.

Self-talk and cognitive behavior techniques can sometimes do me more harm than good. When I am panicking, no matter how many times I incorporate positive self-talk or implement cognitive behavioral techniques, (e.g., replace negative belief that is a falsehood with a true reality-based belief), my body continues to respond as if I am in danger. When I do in fact implement the self-talk, in an attempt to do the “right” thing or to “fix” myself, I then feel guilty when the technique does not work. I then question why I was not capable of applying such a simple concept to my own way of thinking.

No amount of practice, hard work, or scouring through books has increased the effectiveness of cognitive-based therapy techniques for me. And the more I use them, and fail, the more I feel as if I am wired in a way that is wrong.

What does help me is letting go and realizing that the panic is something I have to go through, and realizing that when I am on the other side I will be okay. And that there is nothing wrong with what I am doing or going through. It is just the way I am. So in a way I am using positive talk, but not in the traditional sense. I am not finding a false statement or belief that needs change and fixing it. Instead I am self-soothing and reminding myself I will be okay regardless of how I feel at the moment.

I use my thoughts as more of a security blanket. The best thing for me to do in times of anxiety is not to retrain my brain to talk better to me, but to retrain me to treat my brain better. The key being letting go and acceptance.

3. Thinking if I am more self-aware I will be able to control my thoughts and/or anxiety:

I can’t control myself sometimes. I thought if I read enough and studied enough that I could reprogram who I am at a core level. To a degree, spiritually and perhaps energetically, and maybe even genetically, I might be able to alter myself, depending on what doctrine I deem to hold some semblance of truth, but overall I cannot change this elemental core of Aspergers; and if I feasibly can, the answer repeatedly stealthily eludes me.

I have tried every way imaginable to knock some sense into me when I go into a mode of shutdown, and there is nothing I can do, beyond pushing through the uncomfortable emotions.

When my anxiety is high, I become immobile. I cannot do simple tasks. I become extremely fatigued and unable to think in a linear fashion. I become trapped in a cycle or loop of thought. I can step back and see myself doing this. And the odd part is, I know what tools to implement that should supposedly pull myself out, but I also know they won’t work on me. I have tried. Nothing works to stop the anxiety when it is in full swing. It is like I have to go through the tunnel of darkness to come out cleansed and regenerated at the other end.

Days filled with too much sensory overload lead to days of shutdown. During this time life seems bleak and not worth living; however, it does not feel hopeless. I feel fed up more than anything, and exhausted by thought and life. My good hours are usually from when I wake up until mid-day. By mid-afternoon, I often become overwhelmed. This is when I can do little more than sit on the couch. I cannot listen to someone talk for long. It is like I am a computer and all my memory has been filled up. There is no more room left for input.

I have thought to scribe a list to remind myself during the high-anxiety, shut down times of what I need to do to feel better. However, when I am in shutdown, I know that no list of any sort will help. It doesn’t matter that I know why I am overwhelmed and exhausted. My brain is in lockdown. I am protecting myself from short circuiting. The last thing I need is logic or steps to follow. This cognitive reasoning only leads me into further shutdown and retreat, further bombarded by the outside. The only method that works for me is releasing control and letting myself go through the emotional process. If I do not let myself retreat, I will likely have a meltdown, in where I shout and cry. I need time to decompress and be alone. Time to process and discard of my abundance of emotions and thoughts.

4. Thinking that by knowing I have Aspergers I will be more likely able to change myself.:

With self-recognition of Aspergers my behaviors have shifted, but I haven’t changed. Before I didn’t understand my emotions. Before a major event, like a party at our house, when I didn’t know I had Aspergers, I would get extremely controlling and high-strung. I would order my husband around and start arguments. I would create chaos so I could release the tremendous fear building up inside of me. I didn’t know the fear was from thoughts of the upcoming events. My husband would often ask me why I was so angry and touchy before a party. I didn’t know. I thought I was a controlling person and needed everything to go my way to be happy. The problem was I knew innately I didn’t want to be a controlling person and I was never happy, regardless.

It wasn’t until I realized I had Aspergers that my behavior changed. Now, before an event, I no longer subconsciously create drama so I can release emotion. I didn’t consciously decide to change this; the change happened naturally with the discovery of my Aspergers. Now, I am hyper-aware of why I am upset. I recognize my emotions in detail and the triggers that set me into a state of anxiety. It might seem that knowing myself more would make the anxiety level decrease, but actually the anxiety is more intensified, because I am no longer subconsciously utilizing displacement. I am not displacing my own dread about an event into another event. I am not using or finding a scapegoat. I am not creating drama in order to diffuse my own tension. Instead tension keeps building and I have no way to release it.

Now that I am more aware of my own behavior and emotions, and the triggers, I do much more stimming, e.g., I flick my nails, flap my hands, clear my throat, click my teeth, and so forth. I also have anxiety dreams related to a planned event. And the day of the event, I have extreme fluctuations of emotions, and sometimes physical symptoms such as hives and/or stomach aches. I am now taking in the full of the experience and my body is responding. I don’t know if this is better or worse than the displacement. What is also happening is instead of “freaking out” before an event, I am often “freaking out” after the event. I feel very much like a child who holds herself together for the better part of the day, only to go home and have a meltdown.

I have found, to date, the best way to handle my anxiety is to not turn it into the enemy, or something to be eradicated and ejected, but something to be accepted. The more I fight the anxiety, the worse I feel, for there isn’t any avenue that saves me or leads to rescue. I have to go through the discomfort in order to feel relief. The process is similar to a minor panic attack or adrenaline rush, but it passes, and the more accepting I am of the process the quicker it passes. I’ve noticed the same with my dog’s epileptic seizures. They used to last up to twenty-minutes; now when they begin I hold her and release my own fear. I accept she will go through the seizure and be okay. I send this feeling of acceptance to her, and do not fight her seizures. I then let her go, or hold her less closely, and ignore her in a compassionate way, as if telling her: This is not a big deal. Don’t give it power, and it will pass. Since incorporating this method, my dog’s seizures have decreased drastically in length, generally only five minutes, and sometimes less than a minute. My own anxiety is like a my dog’s seizure; if I just let go and trust it will be okay, it passes much quicker.

5. Believing that by making plans I will feel more structured and therefore I will experience less anxiety:

Sometimes lists help me; especially if there are no deadlines on the list. I like to make lists of chores or errands, and to cross out items as they are accomplished. I also like to rewrite new lists and to see how much the to-do items have diminished. Lists are my friends. Appointments on the calendar are not my friends.

I remember my father would always tell me a similar thing. I would ask him if we could get together on such-and-such day, and he would typically respond that he couldn’t tell me yet, and that deciding at that moment didn’t feel comfortable to him. He did better with last-minute plans. I didn’t understand at the time why my father acted this way. I felt cheated out of his life and not important enough to plan for. But today I understand my father more. He didn’t want to make plans because he didn’t want the stress of worrying about an upcoming event. I am the same way. I have been my whole life.

To me, the best days are days nothing is on the calendar. Even one appointment or obligation can make me anxious for hours beforehand, sometimes even days beforehand. The thought of having to pick up my son up from school each afternoon causes me stress. I leave at a set time daily, and the trip is short, easy, and non-eventful, but the stress does not dissipate.

Usually two hours before a scheduled event, I start to become very preoccupied with the time and the steps I will have to take to leave the house. Simple tasks, like showering or getting dressed, feel overwhelming. I can spend several minutes, processing and reprocessing the pros and cons of showering. I can create in my mind a half-dozen scenarios of what sequence I should follow in preparation for my departure. Even before I’ve started the process of getting ready, I am often mentally exhausted.

When I see an event on the calendar, I have a small panicky feeling inside, as I realize that soon in preparation for an event, I will experience something similar to post-traumatic-stress-syndrome.

This seems contradictory in nature to me: the fact that I do well knowing what to expect and with routine but at the same time I dread plans on the calendar. I look forward to well-structured days indoors at home. However, the repeated isolation and lack of adult company can lead to depression and feelings of isolation, loneliness, and inadequacy.

There is a continual pendulum of want inside of me. On one side there is the longing for company and stimulation outside the home, on the other side there is the longing to hibernate and not have to experience the anxiety involved in going out. This pendulum moves back and forth. If I am not careful, I can self-punish myself by wishing I was different and more normal. I am in a constant state of fluctuation, never centered, and always wanting.

6. Believing if I can just let go of Aspergers and get on with my life, I’ll be fine.

I joke with myself sometimes. I think if I write enough and share enough, I will process the Aspergers right out of me. Some silly part of me believes I’ll wake up and be cured of Aspergers, and if not cured, so much better able to function. The truth is I don’t need to be cured. I am not sick, or ill, or broken. I have been born with a brain that is different from the general population. If society was different, I would be responding differently. But society isn’t different.

I have tried over and over to change myself, to try to fit in, and to try to function, but the more I try, the more I find myself battling the same resistance. What I have found that works is contact with other people who understand me. I feel safe with most people with Aspergers, and to a degree safe with people who would classify themselves as a bit “quirky” or “shy.” I fit nicely with the odd balls and misfits.

I don’t need to let go of Aspergers, I need to let go of isolation and thinking there is something wrong with me to begin with. The more lovely souls I meet with brains wired like mine, the more I learn to appreciate my uniqueness and beauty, and the more I recognize the depth of my own intelligence and empathy.

I was created differently, but different is not wrong, and need not be terrible. With the right balance of release and acceptance, and with the right connection with like-souls, I am learning to navigate myself in this world. Where I used to believe I was dropped down on the wrong planet, I now believe that I am right where I am supposed to be.

299: The New Day

I’ve decided
I’ve decided that you deserve more
More than what I am offering
With my clinging and self-doubt
You are not the key to my self-worth
So I shall work on being less dependent
On you
I am ready to pull away some
I think
I want our friendship to be nurturing
And I am tired of being so needy
I understand what is happening
I am self-harming
Through you
I build you up into someone you are not
So you can disappointment
Or rather
So I can think you are disappointing
For then I experience a rawness inside
A Terrible Ache
That reaches into the heart of me
It is only then
With the coming ache
That I feel alive
Without this intense angst
I feel numb
For no one can fill my depths
With the love I need
And thusly I am left hollow
And alone
In desperation and with desire
I grasp on to Love’s cousin
Pain
And pour him into me
I use
My addictive substance
Over and over
To exist
Because I feel alien
In this world
In both form and experience
I have been using
Using you
To feel real
Using
To wake up
My sleeping soul
I am sorry
For clinging
For aching
For suffering
Through you
But I still choose you
I choose you again and again
Only this time
You are chosen
For your beauty alone
For your light that shines through
The darkness in me
And opens my eyes
To the new day of us

~ Samantha Craft, January 2013

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298: The Weight of Me

I don’t understand my body, what it looks like, what others see me as, how I am supposed to look, what is expected, what is healthy, what is normal, what is standard, what is right.

There is a layering of problems associated with my body image.

1) No Norm Exists

No norms exist related to body image except what society, or more so the media and advertisement companies and other corporations want me to buy into. There is a belief system that varies from year to year, dangled in front of me. I don’t want to be a fish: a hungry guppy rising up to take hold of some enticing treat that will likely gorge me, stab me, break me, or result in me being sliced open, gutted, and fried to a crisp. Nor do I want to see the bait. But everywhere this bait floats about, the hook hidden and waiting to damage.

2) I Have a Degree of Body Blindness

It is hard for me to see myself as a whole, and to see others as a whole. I can see when someone has some extra padding, a few extra pounds beyond this societal standard of ideal weight, but I can’t hold the whole of someone’s image in my mind. If I was asked to sketch a body, I could not. Everything would be out of proportion, including the length of the arms and legs, the scale of the neck, and the angles of the face. Everything I take in is somehow mutated and rearranged, so that what I recall in my mind’s eye could likely be a Vincent Van Gogh painting. I cannot see my own body, clearly, as well. I rely too heavily on the eye of a camera, only to have discovered as of late that the camera is not an adequate portrayal of my weight, as the aspects of my clothing, the way I am standing, the angle of the camera, the type of camera, the lighting, and even my mood, posture, and expression, affect the end result (the photo image).

I’ve studied myself in photos for months, and still am baffled by what I look like; and how I look to myself, changes each and every time I glance at my reflection. And even the reflections are deceiving; how I appear in the rearview mirror, the glass of a window, or from one bathroom mirror to the next, always shifts, and I find a new person staring back at me, reversed and bewildered. I am left to wonder where the real me exists. In front of the full length mirror I stand, turning and processing, in awe of the stranger standing there. Photos will generally depress me, as they do not seem to represent who I see myself as. And worse, I can’t really see myself at all in form. I am like an unformed mass, shifting as the flowers and plants vary with the seasons. I cannot find myself, as hard as I seek, at least my outside self; for I seem as mysterious as the birth of the universe, as infinite, and as ever-changing.

3) I latch on to rules and examples of beauty even though the societal norm of perfection is unattainable

I have been brainwashed. I have been bombarded with images of what I should look like. I have been told, in the form of photos, movies, sitcoms, commercials, advertisements, magazine covers, billboards, department store displays, peers’ behavior, and various fix-yourself-now articles, that I am somehow wrong and in need of repair. In addition, I have been informed that if I go through various steps, I will then be adequate, and once adequate I shall be accepted, loved, and adored. I have seen this “beauty” scenario unfold and be reinforced when I was a teenager; seen how the people around me responded and took note of me if I was dressed the “right” way, if my hair was “good,” if my makeup enhancing, my body shapely. I have seen the attention that the socially accepted “beauty” brings. I have also seen and felt how empty the experience of acceptance based on exterior beauty alone can be, seen how fickle and cruel the shallow admiration is. I have felt like a tree adorned for the holidays, sparkly and the center of attention, only to be later tossed to the side of the road waiting my fate. But still, I have this brain, some type of organizational system working inside of me that searches for the “rules” the standards, the way to exist on this planet and in this society. I think, deep within, that if I can find the right path, I will fit in. Yet, I am faced with an unhealthy path; one that leads to imperfection after imperfection, and demands my money, and worse my soul.

4) I exist at one extreme or another

The place of middle ground in all areas of my existence is foreign to me; as hard as I study and try to get there, I cannot. My mind works in extremes. I am generally high or low, calm or hyper, still or moving, cautious or daring, charming or a pain in the butt, loving or stand-offish. The in between space baffles me, and analysis of the concept of middle ground leaves me stranded in thought, wondering why I cannot be “that way,” the way of the masses, the way of the easy life.

Though I try hard to find balance, I continually find myself swinging on the spectrum of intensity, the volume of my every minute, high or low; the intensity affected by the tides, the planets, the food I take in, the music surrounding, the sounds, the energy of other people, the thoughts roaming within, the expectations placed on myself, the voice that rises and interrupts my doing, the inconsistency of trying to be, and the varying degrees of living in the moment.

I am unsettled. Every inch of me unsettled. And like the shifting of my body image in my mind’s eye, my state of being shifts. My efforts are circumvented by the infectious factors all about me. In being this way, I take on tasks with a high degree of interest or I give a task no regard whatsoever. This, this taking on of tasks, applies to the way I manage the weight of my physical body. I can be extreme for months with a diet, avoiding certain fattening and bloating foods, avoiding sugar, avoiding all junk food, avoiding grains, etc. But I can only exist in the state of extreme for so long, and then I break, and where I had felt to be in a constant state of fathom, I now emerge into a state of feast, starving and deprived. My weight fluctuates depending upon where my pendulum of intensity exists. I am at the mercy of my passion or lack of interest.

5) I feel better at my ideal weight, but the definition of my ideal weight varies depending on source.

I would like to say that I am comfortable in my own skin, but I am not. I have latched onto an ideal number for my weight based on how my clothes fit and how I appear in some photos. Not all photos, because even my ideal weight looks odd in most images. To me, when observing myself, I can appear obese and bloated, even though I am told I am skinny. Ideal weight is listed and available on medical charts. But this weight standard is obsolete. I have always been much heavier in scale number than I appear in form. I was stick-skinny in high school, skinnier than most everyone, but I was heavier on the scale. I am 5’ 4” and in the last several months average about 139 pounds. This is a high weight for some people, but for me I can fit into size 4 or size 6 pants. For me this is thin. At 137 I start to appear gaunt and unhealthy. I know that I appear best at 139 pounds even though this amount weight is repeatedly reinforced in movies, magazine articles, and charts as “heavy.”

I am confused by contradictory data, and contradictory data is everywhere. There are sources that say it is good to go into menopause with weight around the belly, and some fat on the bones, as this decreases your chances of bone loss. I have read it is natural and healthy to have some excess body weight as one approaches their fifties; yet so many studies warn of various diseases and fatalities if the weight is not monitored and controlled. I look back at paintings from the centuries before, and think the voluptuous women look lovely. I look at the stick-skinny, starving-themselves women, and think they look stern and unhappy, rigid and angry. I look at myself and don’t know what I think, beyond a woman struggling to find the “norm” and what is “right,” in a world with variables and contradictions.

I latch onto numbers. So I latch onto 139 pounds as my standard, as my ideal, as my place to be. But I have a slow metabolism. I can eat one meal a day and gain weight. Is my esteem wrapped up in my weight? I don’t think so. I think my esteem is wrapped up in the unattainable image I think I am supposed to attain: an image I cannot see in my mind’s eye, an image that is deceptive, contradictory, and unachievable. I am not wrapped up in looking skinny or attractive enough, I am wrapped up in trying to figure out what I look like to begin with, how to keep a number on the scale from fluctuating so I feel stable in a very non-stagnant world.

I just want to fit in, or more so blend in. I don’t want to stand out for a perceived “negative” attribute; I don’t want to be unhealthy; I don’t what to exhibit gluttony; I don’t want to appear “wrong.” All these “norms” and expectations I set upon myself. And I don’t know how to turn the voice of expectation off. How to just be with me. How to just love me. How to see I am not this vessel that ages daily, slowly deteriorating towards death.

6) I set different standards on myself than other people.

I logically can tell myself that I do not care what others look like, and this is the truth. My dearest friends can be any weight, and they are just as lovely and beautiful to me. I don’t take notice of people’s weight as much as their eyes or their kindness. I love all shapes and sizes, and find attributes that are unique and different to be interesting and attractive. I like a woman with a little fat on her, personally. And if I were a man, or a person attracted to women in a physical way, I would choose someone for their inner beauty and character, not for their weight. Weight would not be a factor at all. And as a female attracted to men, I am not attracted to the weight or fitness-level of a man. At this point in my life, I could be in a romantic relationship (if I wasn’t married, of course) with any shape or size, any ethnicity, and any age (within reason).

The outside exterior of another, male or female, friend or stranger, no longer affects me like it did in previous years. I see the collective person: their soul, energy, purpose, drive, love, heart, etc. all interwoven to produce a beauty. Yet, I cannot do this with my own self. Make myself see my collective beauty.

I know I am lovely inside. I know I have a huge heart, massive amounts of sensitivity, compassion, integrity, honor, and love, but yet, when I evaluate my own beauty I go back to this fictitious number on the scale.

7) I don’t know where to turn for help.

If I let go of my rigid goal of maintaining a certain weight, I would gain weight. While I might be able to learn to feel comfortable in my own skin when I am heavier than now, I face other complications as I gain weight. When I add on pounds my chronic fatigue and chronic pain increases, exercise becomes harder, and just moving in general is burdensome. When I gain weight I do not recognize myself, or rather I recognize myself even less, and I am confused when I see my image.

However, while striving to maintain my weight, I put unyielding pressure on myself of what to eat and what not to eat. I punish myself for cheating. And for me cheating is having organic cheese puffs instead of organic red peppers with my humus. I tell myself terrible messages, such as I don’t have willpower, I am going to gain weight and no one will love me if I am not attractive, I will forever be alone, and on and on.

In addition, food affects me drastically. I cannot eat anything, beyond pure protein, without having instant pain and fatigue. So, I often go most of the day without eating, because as soon as I eat I have a reaction, in that extreme fatigue sets in coupled with pain in my muscles and joints. I have tried many different diets, food combinations, etc. for many years, to no avail. I have come to the conclusion that I am allergic to earth food, and that’s just the way it goes. For me eating fruits, nuts, and vegetables all day is the best, but I crave more.

There aren’t any answers out there. I’ve searched and searched; I’ve waited. I’ve dug deep inside. I’ve meditated, medicated, supplemented, detoxed, etc. I finally reached the point where I believe the best thing for me to do is to stop analyzing my diet and being so extreme. But that’s what scares me; for when I let go, the weight comes back, and so does the resulting painful effects. I’m searching for that state of limbo, where I can just exist without effort, without constantly trying to rebalance, where I can just be. But even the searching hurts.

8) I find my security in the number on the scale.

You could tell me I’m lovely. For a short while I would bask in your compliment. But then, the words you gave to me would fade away, and within a day, or sometimes hours, I would no longer feel your compliment. Instead I would wonder once again if I was truly too ugly for this world. I know this sounds absurd, but this is the untruth that plays out in my mind. I do not understand what I look like, and thusly do not understand how you perceive me. And everyone perceives me differently based on their own life experience and developed tastes and biases. Everywhere I go, I know if someone takes note of me, I am being evaluated. And I dislike that invasion and aspect of being in society.

I want to be seen as the interior me, but am forced to be first presented dressed in this physical essence. In some ways my weight is the only thing that I can control about my appearance, the only thing I can keep the same when all about me is shifting. The rest of me, beyond the finite number on a scale, I cannot see or determine. I cannot find the truth of what I am on the exterior, and so the only security and constant I can return to is the number on a scale. I have a lot of dependence on the number.

It’s not that I want to control my weight; it’s that I want to control some semblance of my existence. I want to understand my physical being, even if it’s only one small aspect, one three digit number.

Everything changes so much in my world from moment to moment, from thought to thought, and event to event, that numbers have been my security blanket for years. So, yes, the number on the scale is my enemy or friend. As it climbs I fear the future, and as it decreases towards the “ideal” I know I am moving forward towards a part of who I was or am. The further I am away from the number on the scale that I have decided is “the number,” the further I am away from my own sense of self.

I long to find my security for my physical self somewhere beyond a number and beyond an image. But I often wonder, if I cannot view this illusion of self, then how can I be secure. Rather it is acceptance I seek. Acceptance of the unknown and the release of my dependence on outsiders to quantify who I am. An acceptance in the knowing that although I am invisible in regards to my appearance to physical self, I am solid in my understanding of spirit.

297: Symphony of Sorrow

The glacier unleashed above the surface, exposed to the elements, withered and melting, as ice teeth drip in sun dagger’s game

The fortress unmoved in storm, harbored deep into the rooted ground by intertwined redwoods eating away at the past through methodical digging

The opening beyond the passageway, circumventing the avenues of darkness, though blind, a serpent worm hollowing and sharpening the narrowness below

The salutation circled on parchment dry, driven in passion by black-tipped feather dancing its way across the pages of time

The window frame broken, cracked over with windy days turned blizzard, and painted false with robin-blue, layer upon layer, until chipped and exposed the ruined beginning bleeds

The casual handshake of palms fleshy and ripe, with sweat and history intermingled more than the strangers that touch

The blanket hung upon the clothes line, overlapped and moving in the breeze as ghost sheets whisper their jealousy, wanting the warmth to move through them, like champion fingering the goblet of victory

The breath of the sailboat, weeping for the coming of wind, where tossed and turned the sails shall bellow in defense, when all about the observer grins, thinking the movement enters sweet without cost

The misery belonging to one, the performer across dimmed stage, spinning in the absence of light, invisible to the onlookers, if audience ever entered

The broken, spread out for picnic, picked apart to bone, and left for the army of insects to devour the remnants of screams harbored in the feast of gluttony

The fear reaper, echoed shadows of past, silk and web interwoven to glisten and capture, to call forth and entice, until prisoner bewildered in entrapment pleads for escape

The moment, shaded eyes beseeched lost maiden and all searching tumbled outside of tethered pockets, pebbles touching down into river rapids, one after the other, exiting their chamber of ages

The stallion and steed, a chance glance past the soured fields and dank sky, remembering once together they moved free as drifters in hope’s lullaby

Until now, each as forgotten tune joins to create a symphony of sorrow, their music precise and purposeful, reaching into the severed opening of lost child, and soothing the reflection of their collective pain

~ Samantha Craft January 2013