Birds, God, and Faith.
31 Oct 2010 10 Comments
in Love Tags: belonging, God, Love
Alienhippy’s most recent (lovely as usual) post spoke of how a chicken rekindled her faith. That reminded me of an encounter I had with a little bird many years ago:
One day about thirty-eight years ago when I was a student, I approached the twelve story glass, steel and concrete tower that my class was in. Just as I neared the door a little sparrow hit the second story glass and fell to the ground as if dead.
I dropped everything, forgot about my class, and cupped my hands around the little sparrow. I held it against my beating heart as I sat down on the sidewalk with my back leaning on the building. I hoped some energy might transfer from my heart. After twenty minutes the little bird opened her eyes. Then she began to look around. Next she was sitting up and then standing. At about the forty minute mark she took off, flying perfectly. I never did get to my class.
I imagine one or two of the many people streaming into the building must have thought I was nuts sitting there with a seemingly dead sparrow clutched to my heart. But I know that I was witnessing God’s hand. He brought that little sparrow and me together just so we would both know His deep love and care.
Trapped in a Pressure Cooker
27 Oct 2010 10 Comments
in Asperger's, autism, burnout Tags: Asperger's, autism, burnout
Trapped in a pressure cooker that was about to explode! That is how I felt for a few years leading up to my Midlife Autistic Burnout. I couldn’t see a way out, and I knew I was in very serious trouble — life threatening trouble — where I was.
THE PROBLEM:
The future looked bleak and scary. My health was rapidly deteriorating as I tried to function as a child protection social worker in the Neurotypical world. I could not imagine any other work, in our rural area, that would enable me to continue to support my family. Every career change I could see, involved a substantial drop in income. My wife and I were in agreement about homeschooling, so I had to be the sole breadwinner. We, at the point of my burnout, could not have switched duties because my brain was so fried that I was not able to teach. Jobs available to my wife in our area would have paid too little. Perhaps if we moved to the big city I could have gotten another data analysis position. But both my wife and I preferred the country over the city, for both ourselves and our children. And the city is an almost insurmountable hazard to this Aspie/autie. There is a reason I was attracted to rural life. I need the peace and quiet.
A couple of other social workers, who had lots of connections, and were laid-back extroverts, left the agency to become insurance salesmen, but Aspies need not apply! And an NT friend, and fellow social worker, commented that the job took so much out of us that there was absolutely no energy left for job hunting.
The present was unsustainable. I was having chest pains, palpitations, migraines so bad I would have to pull the car over and vomit, so little endurance that I had to squat or lie down on the floor to avoid a faint after any unusual exertion (this was really embarrassing in stores), extreme memory and cognitive deterioration, inability to sleep more than three or four hours (and no deep stage 3 or 4 sleep at all, and that’s where our body/mind rebuilds), subnormal body temperatures (chills) or chronic mild fever, sudden drop in blood pressure. I better stop, but the list goes on and on. My doctor knew I was in deep trouble and counselled me to stop work, take a break, and make a career change.
THE SOLUTIONS:
Physical exercise: I actually enjoyed exercising when young. But all attempts were a disaster during my burnout. They would literally put me on my back for days.
Trust, faith and hope. I was a believer and a practicing Christian at the time. I knew the benefits of dwelling on the positive, trusting God to look after the future, having faith that all will be well, etc.. But in my mind-numb downward spiral towards death (I’m not exaggerating) I have to admit that I couldn’t generate enough faith, hope or trust.
Creative alternatives: My doctor knew I had paintings hanging in several galleries at one time and that I loved driving. She encouraged me to consider art or truck driving. These occupations would have been much more fun than child protection, but they wouldn’t have paid the bills. And the fact is I had deteriorated so much by then that I could not have functioned in any occupation.
Get rescued: This is what my doctor, bless her soul, did just in the nick of time. She told me I should stop working. I didn’t want to stop because I had my family to support. So I worked out a scheme with my supervisor whereby I would work halftime. When I returned to my doctor a week or so later and announced this scheme, she yelled at me, “YOU HAVE TO STOP WORKING!”. I had never seen her get angry in the thirteen years my wife and I had been her patients. We also brought our children to her, and we always appreciated the way she would say, “I don’t know what it is,” on the rare occasion when some illness was puzzling to her. That gave us confidence that when she did make a diagnosis it was correct.
MY RESPONSE:
Listen to my doctor: I decided that I had better listen to my doctor. I went back to my office, picked up my briefcase, walked out to the parking lot, got into my car and drove home. The next morning I telephoned my supervisor to advise him I was now on sick leave. That led to getting Long Term Disability Insurance Benefits for seventeen years until I reached retirement age. Even the insurance company doctors said I was “totally disabled” (unable to work at all) and that I would probably never recover.
THE OUTCOME:
Still here: Well with extraordinary, sacrificial support from my wife, and lots of help from my kids, and a level of care from my doctor that was “beyond the call of duty” (she even gave me her home phone number), and help from various specialists, etc., I am still here and I am HAPPY!
Praise the Lord!
Burnout.
24 Oct 2010 9 Comments
in Asperger's, autism, burnout Tags: Asperger's, authenticity, autism, burnout, expectations
Burnout. This is a piece about my own burnout. I am writing in the hope that anyone struggling with burnout may find something here that may be helpful.
I remember, many years ago, reading a sidebar in Scientific American. I don’t remember the main article but the sidebar stuck in my mind. It was about a study of stress in monkeys. The experimental group was stressed by loud sound and the control group had no stress. At the end of six or twelve weeks (I’m not sure of the exact time, but it was short) the stressed monkeys were all found to have lesions in their brains but the controls had normal brains. In short, stress actually caused brain damage. (But do take heart, recent research into neuroplasticity has revealed that our brains are very good at building new circuits around the damage).
I heard a piece on the radio the other day about an author who was writing a book about his research into an actual gruesome murder. He would work on it until midnight. Then he would feel that he needed a shower or some way to disinfect himself. His wife finally told him that he needed to take a break from the book. She could sense the toll that dealing with the horrible facts day-after-day was having on him.
I once worked for ten years as a social worker in child protection. I would usually wake up at three in the morning thinking about my clients’ situations. My wife wondered how I could exist with only three hours sleep a day. The fact is that I couldn’t, as we eventually found out. My family physician sent me to several specialists over several years trying to find out why I was getting progressively weaker to the point that I did not know if I would make it all the way to my car, without collapsing, while carrying some milk from the supermarket. I was also having progressive, profound memory and cognitive difficulties. It got to the point where I had to take written notes when discussing a case with my supervisor, and then reread my notes before going into a clients home, and then take glances at the notes during my interview to make sure I covered everything. And I used to be one of the top investigative workers in the agency! Over time, as I gradually went more and more down hill, my doctor finally, in 1993, diagnosed Chronic Fatigue Syndrome (or Myalgic Encephalomyelitis as it is known in Commonwealth countries).
Then she sent me to someone who specialized in CFS/ME. He was reluctant to confirm the diagnosis because he was picking up strong signs of burnout. So he sat on the fence for a year, and I carried both diagnoses. Then after a year, he said that I should have recovered from burnout by then so he settled on CFS/ME. The Long Term Disability Insurance I had at work tried everything to rehabilitate me but to no avail. They considered me “totally disabled” which meant that I was unable to work at any occupation. I collected LTD benefits for seventeen years until I reached retirement age last January. I say that just to give you an idea of how severe the disability was (insurance companies don’t like paying out benefits!).
Since joining the Autism Spectrum blogging community, I am seeing CFS/ME as probably a misdiagnosis. My doctor’s original hunch about burnout was probably correct. But hardly anyone had heard about Asperger’s back then. Profound Mid-life Autistic Burnout is what I believe I experienced.
My clients would tell me that I wasn’t like their other workers. They said I cared about them. One mother, whose children had been placed in care, told me I was too sensitive for this line of work. They were seeing the highly charged empathic response of Aspies/auties. Our overactive brains take in too much, and process it so thoroughly, in such a highly charged manner, that I believe we risk burn out. Especially when day-to-day work involves exposure to so many tragedies.
Caution: the next paragraph contains a description of an abused child.
I have memories, of things I saw, and disclosures I heard, that are still vivid after all these years. I can still picture the back of a little three-year old girl. Her babysitter called us because the girl’s back was crisscrossed like lattice-work by raised red welts from her mother’s belt. I can see that little girl in my mind today as clearly as I saw her in real life 25 years ago. I will carry her memory to my grave. And that’s not to mention all the disclosures of physical, emotional and sexual abuse.
There was also the extreme stress of attempting to function in the neurotypical work world. In the course of investigating child abuse I interviewed children, perpetrators and parents. I participated in case conferences at the agency and at hospitals. There were staff meetings and visits to foster homes. I often testified in court. I was on the union negotiating team.
But I was also known as “the invisible worker” by some of my colleagues because, at lunch, I retreated to my office to recoup and recharge, rather than socializing in the staff room.
I had great difficulties getting my paper work done. When I should have been writing a report I would find myself just sitting there at my desk while in my mind I was off in some fantasy world much more to my liking. (but on rereading this, I ask myself who wouldn’t want to escape the world of child abuse? but I still struggle with getting things done because I really like my fantasy world!)
Little did I know that my differences, which I tried so hard to cover up and overcome, were actually signs of autism/Asperger’s which I should have been celebrating. Had I known then what I have just recently learned from the autism spectrum blogging community, perhaps I might have been able to accept my differences, and live accordingly, instead of trying so hard to behave like a neurotypical. I am not sure how I would have earned the income needed to support my homeschooling wife and four kids, but perhaps something creative would have occurred to me. There was so much needless stress caused by attempting to be what I was not. My attempts virtually always fell short of my expectations, which in itself increased my stress. And the price I paid was high.
A professional suggested once that people like me, whom he diagnosed as Socially Phobic, belong in backroom research laboratories and computer labs. Before moving to the country I worked as a data analyst on a research project. We had a four or five person team meeting for two hours on Tuesday mornings to update each other, and outside of that meeting I never had to talk with anybody! The rest of the week I worked at home and in the computer lab analysing data. My wife helped me with the data entry, which reduced my workload and hours. I did talk to her, but I liked that. It was the best suited job I have ever had!
So if you struggle with burnout, please be careful. Be gentle and kind to yourself. Keep your eyes open for a creative solution that honours your own true beautiful makeup.
(Edit Nov. 20/2010: I originally wrote this because a blogging friend seemed to be going through a burnout, but it turned out to be a different medical problem so I modified the post accordingly).
Fitting in.
20 Oct 2010 8 Comments
in acceptance, Asperger's, autism Tags: acceptance, Asperger's, autism, belonging, body language, fascial expression, loneliness, tone of voice
Fitting into group situations has often been a problem for me. Here are some of my thoughts on this:
Body language, facial expression and tone of voice:
I once worked with a team of five or six guys and there was a lot of kidding around, teasing, and playing of practical jokes. They would exchange what would, on the surface, appear to be insults, but everyone would laugh good-naturedly and joke back. Whenever I tried to join in, it seemed to put a damper on the situation and the group would disperse or get back to work. They seemed to take my joking as if I were being deadly serious.
It took me a long time to realize that I tend to not display much facial expression and my speech is close to a monotone. Because I am uptight in social situations my body is tense rather than loose and expressive. With a flat face, tight body, and a flat voice, I came across as very serious. My “joking”, although it did not differ in content from the other guys’ joking, was perceived as an insult because it was accompanied by serious-looking body language and facial expression, and a serious-sounding voice.
Thorough, and therefore slow, cognitive processing:
I find it difficult to process the conversation on the fly. My mind needs lots of time to digest what was said and to explore every option. It takes me a long time to think up a thorough response to the ongoing conversation. I tend to weigh all the alternatives and carefully formulate a creative and intelligent response.
But by the time I get my answer out, the group has gone on to a totally different subject and my response seems so out-of-place. They have left the former subject behind and are often reluctant to revisit it. Hence I feel quite “out of sync”. Of course, by so thoroughly digesting the former conversation in my mind, I have missed half of the current conversation, so I fall even further out of sync with the group.
And when it came to joking, as discussed above, my timing was probably off because the group had moved on to another area of kidding before I had a chance to make my contribution.
Anxiety compounds the problem:
The difficulties compound exponentially over time, as each difficult social interaction makes me even more tense at the next one. Eventually, giving up seems to make sense.
Solutions:
But giving up leads to loneliness, which is not really what I want – at least not all the time. So I try for one-on-one conversations with my family (and occasionally a friend). And I have started blogging, but I guess you know that.
Blogging slows down the pace of conversation to a more manageable level. And I have met some really nice people in the Aspie/autie community.
Noise
16 Oct 2010 2 Comments
in Asperger's, autism, senses Tags: Asperger's, autism, noise, senses, sensitivity, sensory overload
Noise. What most people refer to as sound is often experienced by me as unpleasant noise.
Before I had to go on Long Term Disability benefits many years ago, our team at work would occasionally go out to a restaurant to celebrate someone’s birthday. The noise level at the table was very high and we were surrounded by tables with similar high decibel conversations. When trying to listen to an individual near me at the table, I would not be able to filter out the other conversations. All the sounds just blended in to one confusing noise. If I cupped my hand to my ear I might be able to grasp a bit more of what was being said to me. I am sure they all thought I was quite deaf.
My hearing actually tests out as very good when I am in one of those sound-proof rooms and the audiologist feeds me one word at a time. My hearing falls apart when I have to separate a word from a jumble of words all coming at me at once. My specialist (ENT) says this is a problem in my brain (higher processing level) as my ears are fine.
When my family is sitting around the table socializing I often need to have some “down time”, so I go upstairs and try to read. Unless I put in earplugs or wear ear protectors, I have a very difficult time reading because the words coming in my ears get all mixed up with the words on the page. This also happens if the radio or TV is playing.
If the text reads:
Look! See Dick run. See Jane skip. See Spot jump.
it will come out something like this if the radio is on:
Look! Do you See think North Dick Korea will run See develop nuclear Jane skip weapons and See Spot bomb jump us?
except the colours aren’t there, which makes it even more confusing.
Trying to read under such conditions just sucks all the energy out of me and I am left exhausted with my head hurting and all my brain circuits flooded. I have to put the book down because my mind just can’t cope.
Not all sound is noise to me. I find I can hear one-on-one conversations in a quiet space. And I do enjoy some music very much. There is a tea-room in a small town not far away. The owner plays Baroque or Renaissance music, or nature sounds, at a soft level. I find it soothing. It enhances my enjoyment of the meal.
But when I was at the ENT specialist a couple of weeks ago there was a pop radio station, with a motor-mouthing DJ, playing through a ceiling speaker. I was trying to read a magazine. I felt like asking the receptionist if they had ever surveyed patients’ preferences as to sound bombardment. I didn’t ask because I have grown accustomed to being the odd man out.
Four Pairs of Sunglasses
12 Oct 2010 Leave a Comment
in Asperger's, autism Tags: Asperger's, autism, eyes, sensitivity, sensory overload
Yesterday I posted about wearing four pairs of sunglasses: this is how I did it:
A is a pair of large sunglasses designed to go over prescription glasses.
B is my regular prescription glasses.
C is three rigid thin plastic sunglasses designed to slide behind regular glasses. They are made from sheet plastic and shaped to hook over the top of regular glasses and hang behind. I stacked three of these together and hung them behind my regular glasses.
(note: if the regular prescription glasses were tinted then there would be five pairs of sunglasses).
Glare
11 Oct 2010 13 Comments
in Asperger's, autism Tags: Asperger's, autism, eyes, glare, sensitivity, sensory overload
Glare! Sunshine, blue skies, orange, red, yellow and gold leaves on the trees, and I needed four, yes that is four, pairs of sunglasses to drive home from the big city about one and a half hours from here. I would have used five pairs if I
had another in the car. It took that many to reduce the light hitting my retinas to a bearable level. I am talking about the kind of day that most people would have revelled in with one pair of sunglasses or none.
Bright light, and glare from car windows and chrome, can feel like skewers jabbing into and through my eyes. Even closing my eyelids fails to give relief. Multiple layers of sunglasses or a dark room are my only remedy. Without shades, and sometimes even with, I get stressed and exhausted because the brightness is so unbearable. I just can’t wait to get home and find relief in the shade of our trees or the darkness of my bedroom.
And the outdoors is not the only source of glare. My computer screen is turned down to the lowest level and I still find it too bright so I am typing with my eyes shut. (Thank goodness for WordPress’ spellchecker!). I also find some of the chairs in doctors offices to be a source of jabbing pain in my eyes. These are the chairs with chrome plated metal frames. They often have padded cloth seats and backs. The metal frame reflects the flourescent light coming from the ceiling and I must avert my eyes. There are usually so many such chairs that I have no place to gaze, so I resort to closing my eyes. Even a polished tile or wood floor will reflect sufficient glare from the room lights that I hold a magazine at the correct angle to block the reflection.
I also find myself moving a box of kleenex or a bottle of juice, while I’m eating, so as to block that jab of glare on the table. Sometimes I hide my knife under the edge of my plate because of the brightness. Reflected room lights bouncing off the window at night have me shifting my chair or closing blinds so I can converse with my family.
I don’t personally know anyone else who goes to these extremes to avoid light. So I thought I’d post my reactions in case there are others out there who know what it is like to have skewers jabbed into their retinas. This way perhaps they won’t feel so alone! And no, I’m not in the sunglasses business!

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