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.