Trapped in a Pressure Cooker

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!

10 Comments (+add yours?)

  1. Laura
    Oct 27, 2010 @ 13:18:13

    I’m sorry it got so dark for you, but I think it’s fabulous that you were able to come out the other side. Happy is good. :-)

    Reply

    • born 2b me
      Oct 27, 2010 @ 17:43:18

      Hi Laura, thanks for your visit and comment. I posted this, and the previous post, in the hope that they might be of use to anyone going through a MAB right now. I also had in mind young people — wanted to caution them not to attempt more than they can handle. Also I am attempting to document my experience on the spectrum. It is good to be out the other side. A big part of my new enthusiasm comes from discovering your blog on Freshly Pressed, and also linking to other’s from yours. This opened up a whole new world for me. Thanks! :)

      Reply

  2. Rachel Cohen-Rottenberg
    Oct 27, 2010 @ 17:50:10

    I love this post. I’m well into my healing from MAB, and I feel very blessed that I was able to get out of the pressure cooker before it did me in. Like you, I hope that the folks growing up on the spectrum take better care of themselves than we did. Knowledge is power!

    Reply

    • born 2b me
      Oct 27, 2010 @ 18:43:04

      Hi Rachel, it is really encouraging that you have made such good progress.
      Yes, knowledge is indeed power. And you are doing such a great job getting that knowledge out there!

      Reply

  3. Clay
    Oct 29, 2010 @ 15:20:27

    Glad you made it through. For me, retirement is a blessing. If I were to make an analogy, it’s like getting up after noon (most days), and setting water on the stove for coffee. But only setting the stove to “warm”, the lowest setting, and not “high”. There’s no bubbling, no troubling, just warmth!

    Oh, and I just went the other day to apply for food stamps, and the process was really easy. They’ve downloaded $233 to my Benefit Card, which is to last for two months. After that, I’ll get half that each month. I don’t think I ordinarily spend that much on groceries. I don’t know if any unused benefits “roll over” to the next month. Anyone know about that?

    Reply

    • born 2b me
      Oct 29, 2010 @ 16:06:04

      Thanks Clay. I am enjoying retirement. One thing I like about it is that whenever someone asks “what do you do” I can simply say “I’m retired.” Before, I used to have to say, “I’m on LTD benefits due to CFS,” and a lot of people did not know what Chronic Fatigue Syndrome was, which led to having to give lengthy explanations.

      I’m in Canada so I don’t know the answer to your question about food stamps. Perhaps someone will see this and respond.

      Reply

    • unstrangemind
      Oct 29, 2010 @ 19:32:52

      Clay: Yes, unused benefits roll over to the next month. I asked my case worker if there were a cap beyond which I lose some of the benefits (Because I’m disabled, I also get a small cash benefit on my food stamp card, for buying non-food items.) He told me that you only start losing benefits if you haven’t used the card for four months. Of course all of this is for my state and the regulations in your state might be different. (But are probably the same.)

      Reply

  4. Clay
    Oct 29, 2010 @ 19:33:11

    Got a letter from them today, and the benefits are explained better. The reason they initially gave me $233 was, $200 is for November, and the $33 was for what was left of October when I applied. So, I’m going to be getting $200 in FS benefits every month. woOt!

    I’m sure I’ve never spent that much on food in a month. Just went shopping, and stocked up on meat. Still don’t know if any unspent funds are “rolled over” though.

    Reply

    • unstrangemind
      Oct 29, 2010 @ 19:51:47

      Wow, we only get $198/month for two disabled adults. Maybe because the cost of living is lower here? Still, with my many food sensitivities, it only covers half our monthly food costs.

      Reply

  5. Clay
    Oct 29, 2010 @ 19:35:56

    UM, thanks. I’ll ask my neighbor if the laws are different in NY.

    Reply

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