In my last entry I described dealing with aversive stimuli while in the hospital. By centring myself in a quiet place, I was able to basically ignore the chaos that one is exposed to in hospitals. This is sometimes known as cognitive control and it becomes easier to develop as one gets older. Of course it takes awareness of our quirks and aversions to exercise this cognitive control.
The Red Cross loaned me a shower chair to use as my balance is still not 100%. I put it in a very small shower (barely large enough to turn around in). I turned on the water. The water filled the stall with spray. At that point I realized that I could not get myself to step into the stall. I have a strong aversion to putting my face into water. When I shower, I slowly put my body into the stream but keep my face out of the water. So, I stood there and began to choke up with fear. After a moment I turned off the water and took a sponge bath.
The point of all this for me is Stay aware and be prepared meet all challenges, including some really old ones.
In last November, I was walking 6-12 km. per day and kayaking 2-3 times a week. Then, I had a violent coughing attack while driving. After that, I began to have issues with my arms and my walking started to break down. On Boxing Day I went to Victoria for an MRI of my spine. Two days later they performed surgery on my spine. I am now on the mend and am getting better every day. I can walk and my arms are good.
When I was put in the hospital I informed them that I am autistic. The surgeon placed me in a private room. I was frightened but okay. Two days after the surgery I was moved to a room with three other men. The biggest issues for me were the levels of stimulation; the lights, smells, noise and the food were challenging, along with remarks like I can’t tell you’re autistic or you don’t act autistic.
However, lying on my back for two weeks allowed me to think through a number of issues that I have struggled with for decades. One is so-called “magical thinking”. Like many on the spectrum, I have difficulty seeing the large picture of the world, usually known as the Gestalt. Without having a plan that would dictate what I would need to do, such as my higher education or a job, I would just do whatever I needed to do without thinking about outcomes or consequences of my actions. If, for example, in intimate relationships, it was time to move past the courting phase I would not know what to do so I would sabotage the relationship. I could not overcome my fear of emotional commitment, as I had no idea of what that meant. My inability to see another’s perspective kept me in an egocentric bubble.
Now I understand that everything a person does affects those around us and I need to keep others in mind when I speak or act in a specific way. My partner has been telling me this for many years. I can now more clearly see the issue and will be correcting the issue as it arises.
In future entries I will address other issues that have arisen since this experience has occurred. Thank you and I welcome all feedback.
If knowing my quirks helps me to understand my autism more clearly, then it seems like a good idea to explore them. So, here’s a list of some more of my quirks.
I use the same dishes, forks and anything else I can without changing anything. I do what they call routinize almost everything.
I have a very short attention span if I am not interested in something, and I can focus for hours if I am interested. If I am not interested in what someone is saying, I will walk away while they are talking. Recently I learned that to do this was rude.
Socially, I seem to be clueless.
I seem to be unable to sustain a healthy intimate relationship. When the passion begins to subside I seem to be unable to go to the next level. I have been married six times. Only my current wife refuses to give up on me, although we are currently living apart.
I have more than one special interest. I can talk for hours without understanding when people become bored.
I seem to have little or no common sense. I could never figure out the sayings like “A stitch in time saves nine “. My question was always Nine what?l
I am sure that I have many more quirks. This is an ongoing process for me. I would like to hear from other folks who may have “autistic “quirks.
First, stimming is repetitive behaviour that results in burning off excess energy and helps calm the stimming person. Examples would be body rocking, hand waving, chewing and a host of other behaviours. There is a list somewhere on the internet that lists over 1400 stims. When I was a small boy, my stims were suppressed by my parents and in school. As I began my exploration of my autism three years ago, I rediscovered the different forms of stimming that I used as a child. Body rocking is a big one. However, I have learned to not body rock in public as people stare. It is my hang up, not theirs. I purchased a stim ring which has a ring inside another ring, from Stimtastic.com and it is very effective unless I am very upset. However, the stim that’s always been there, and the one that I use at home is finger chewing. I did not know it’s a stim!
Another “quirk” of mine is my difficulty with “common sense”. A recent example would be walking 200 meters to get water in the winter while camping instead of melting snow for water. Then there is reacting to part of a sentence as opposed to waiting for the entire statement. And of course, walking away from a conversation because I was “finished” talking and has no idea the other person was still engaged in the conversation.
Autistics have all kinds of so-called quirks. The real issue for me is that stimming is normal for Autistics as are other quirks. It does not matter what NTs think. We focus on how to be more comfortable with ourselves. We should be proud of our autism!
When I received my diagnosis I was initially relieved. Finally, I knew why I was “different”. That feeling did not last. As the reality that I am autistic sank in, my core identity began to crumble. Meltdowns replaced my angry outbursts. I became very confused. I felt bombarded by stimuli such as bright lights, which have always been difficult for me, now became paralyzing. This slowly became easier once I understood what was happening.
The initial label I was given was Asperger Syndrome. Everything I had read was accurate. Then, I began to become uncomfortable as it registered with me that the label Asperger Syndrome was for a disorder described in DSMV. Since I do not have a disorder, but am a different neurotype, I chose instead to use the term HFA or high functioning autistic. This label was comfortable until I watched an Ask An Autistic video that focused on the label issue. It was then that I realized the HFA label has an implied judgment “I am higher than you”. Higher in what? Now I am a 74 year old autistic man and I am comfortable!
One thing I have noticed is what people say when they find out that I am HFA. Most are people that I love and respect. However, some of what they say is inappropriate to ask. For example, “You don’t look autistic “. What does an autistic look like? Or, “You don’t act autistic “. Or, “You have been such a success. You can’t be autistic “. I have a good friend who, when she heard my diagnosis, said “It must be wrong. You aren’t autistic!”.
The website Ask An Autistic, with Amythest Schaber has a show about what not to say. This includes the dreaded “Look at me when I am talking to you ” and all the ways autistics are verbally punished for stimming behaviours. Ignorance fuels this type of behaviour. People mean well but they seem to operate on stereotypes. Most older HFAs “pass” as NTs. I am not comfortable passing. I passed as an NT for decades without knowing about my autism. My autism is as much a part of me as are my toes. I celebrate my autism and no longer find passing acceptable. I try to be tolerant of others, something I didn’t do very well before my diagnosis. I now understand the need for tolerance of everyone, including well meaning friends.
Here is a link to Ask An Autistic. https://www.youtube.com/playlist?list=PLAoYMFsyj_k1ApNj_QUkNgKC1R5F9bVHs . I have not received permission to post this but I don’t think there would be a problem.
My name is James Becker. I am a 74 year old HFA (High Functioning Autistic). I was not diagnosed until I was 70. Like so many other older autistics, much of my life has been a challenge. I have worked in many different jobs. I am a retired university level Psychology teacher. My favourite job was driving a tractor-trailer over the road. It figures since I worked alone, driving all night with no interactions anyone. A perfect job for an isolating autistic! I have had run-ins with the law. I have had numerous marital relationships. I have had addiction issues. Lots of issues!
Because autism was unknown when I was born, my parents were not sure what was wrong with me. Both of my older sisters were born with congenital issues (club foot and epilepsy). My father was what we used to call “a stern father”. That translates into intolerance and physical punishment. I was punished and prevented from stimming. Stimming is a form of repetitive behaviour that reduces excess energy and is a coping mechanism. I view stimming as a normal behaviour while most professionals view stimming as “maladaptive”. Of course, NTs (neurotypicals or “normal” brain structure) stim, they just don’t see it that way. In addition, I talked at a very early age (6 months) and did not walk until I was 2 years old , so I must have presented a “mixed picture” to the doctor, who saw me as a bright, small child. Much later in life when I saw a psychiatrist, he didn’t know if he should label me a sociopath or something else. He finally shared that my very high level of fear, guilt and shame ruled out the sociopath label. No Kidding! A high school student could have told me that!
it has taken me about three years to fully accept my autism. What used to disturb me about my autism now makes me smile. One example would be tying my shoes. It is a difficult task for me. Also, I have been told numerous times that I have no common sense, but that I am really smart. That’s kind of like “Look at me when I am talking to you”. It’s one of those sayings that irritate a lot of autistics. I seem to be a bit clumsy and seem to have a lot of bad luck. I break stuff accidentally. I am just now learning how to plan and organize.
I believe that older autistics like myself will want to have a place to vent, seek support or just know that they are not alone. Thanks and 😊
This is your very first post. Click the Edit link to modify or delete it, or start a new post. If you like, use this post to tell readers why you started this blog and what you plan to do with it.
I am starting this blog because I believe there are not enough resources or places for the older autistic to use. The older autistic phenomenon is fairly new, as the focus has been, and should continue to be on autistic children. However, I have found, since my diagnosis in 2013, little or no support for adult autistics within the community (Vancouver Island) and very little online, with the exception of Ask An Autistic. The number of adults with the diagnosis of autism continues to rise. I am a HFA or high functioning autistic. I don’t use the label of Asperger, as it is classed as a subtype of Autistic Spectrum Disorder (DSM5). As I do not view Autism as a disorder, but rather as one neurotype, different from what are called NTs (“normal” neurotypes).
The purpose of this blog is to provide a place for older autistics to express themselves in a safe environment. There are almost no rules.
NO RELIGIOUS DISCUSSIONS!
There are no language rules. I ask that folks remain as polite as possible. We are all autistic!
Thank you and welcome!