[Ed. note: I actually composed the following essay before I wrote Better Living Through References, even though I published the latter essay first on this blog. I intended the essay below to serve as my reintroduction to this blog, this time:]
I have allowed some time to elapse since the last time I updated this blog. That is true for a variety of reasons. In the past few months, I have started a paid internship which has become a temporary job. I am cautiously optimistic.
I am hoping to secure something more permanent while I continue my current work. I am heartened to have something steady while I keep searching, but anxious for the low margin of error I still have. I have faith in the skills that have gotten me to this more positive place, but still feel trepidation for the uncertainty ahead, just as I often have in the last few years.
I've also spent some much needed time relaxing with my friends. In between worrying about my work, whether I can pay my bills, or how I'm going to coordinate my living situation, staying in touch with my closest friends has been more invaluable than ever.
While I have wanted to expand my social circle, by and large, I'm spending time with the same people that I knew when I left college. Another side project, my writing, has been largely hit-or-miss. I've faced prolonged dry spells and feelings of inadequacy, laced with some intriguing experiments and inspirations. I do feel that I have progressed as a person, especially as a young adult seeking to be more independent and responsible. That quest continues to be my main objective.
I have been discussing my interest in the disability community with people from several organizations. My work in health and aging advocacy provides a natural segue to the disability world. I devoured the book "No Pity" by Joseph Shapiro, which chronicles the development of the disability rights movement and describes the challenges that people with disabilities face and overcome.
In parallel to this exploration, I have spent more time reflecting upon my identity as a person with a disability. I have not reached the end of my deliberation, nor do I expect to reach an end - everything I consider is a reaction to the evolving situations in my life, and I relish the opportunity to grow as a person and immerse myself in new experiences (and as clichéd and stilted as that sounds, I believe that attitude and embrace it fully).
So, I am trying to manage all of these different ambitions and necessities before I feel composed enough to express myself coherently on other topics - before I have time, or before I have inclination. I realize this is all elaborate excuse-making, but I also have a cynical faith that the best inventions of human reason tend to be rationalizations. In a last-ditch effort to be somewhat genuine, I am sharing my rationalizations here.
I hope to write more often in the near future. I hope to update this space with something to pique interest. Whether that hope materializes, I cannot predict. I have often hoped on one hand, and schemed to act differently on the other hand. If I have any shot at delivering on these promises, I must scheme to reverse myself again, and return to my original intentions - which change too rapidly to measure.
Yes, those who know me and follow my vain attempts at writing have learned that uncertainty is my crucible and my companion...the catalyst that overwhelms my reluctance, feeds my devotion, and yet, undermines my ability to articulate anything close to the thrill and fervent terror my mind evokes.
My entire life is a somersault: when I dare to reach new heights, spinning in the air to keep my balance, I am stretched so far that I am unable to bring my thoughts to the surface. It is in that brief moment afterwards, when I am standing on solid ground but still remember the sensations of leaping, that I can properly share a true vision of movement.
Okay, that's the round-up of what I haven't been doing, and what I don't know. Eventually, I'll return to tell you about another time when I haven't done something else...
A diary of my crazy, twisted inner life. A forum to vent my absurdity into the world.
Showing posts with label disability. Show all posts
Showing posts with label disability. Show all posts
Monday, September 16, 2013
Sunday, June 17, 2012
Up All Night: Self-Identifying
For many years, I've struggled trying to decide whether I should self-identify in academic settings and in job applications as a person with Asperger's Syndrome. While I've had difficulties in social settings, I always sailed through my academic work until I graduated from high school. I got by pretty well, so I never saw the necessity of raising questions about a "disability", when I wasn't sure that this condition was disabling me at all.
Another issue that complicates my thinking arises when I compare my situation to the situations of other people who have a less high-functioning form of Asperger's. I've been very fortunate. That I can even write these words and tell you about my life is a major success. That I've found the self-awareness to question my own decisions and analyze my interactions with other people has been a major milestone and a great gift.
There are many people who have suffered through much greater impairments than I have. When I perceive that I'm indistinguishable from a typical person of my age, I can hardly justify to myself that I should self-identify as having some sort of disability. The only person I've met who's spotted me as someone on the autism spectrum was another college student with very high-functioning Asperger's -- which is extremely funny once you think about it.
Today, I heard some of my friends discuss some mutual acquaintances of ours who happen to have Asperger's. When my friends mention some of their unsettling experiences with other people who have Asperger's, it's hard for me to discuss my experiences: I'm torn between feeling sympathy for people following a similar outline and a crushing need to defend myself. I know very well that my lack of finesse with social skills in the past has at times brought me great chagrin.
I used to never make eye contact when I was speaking to other people. My dad would sit with me and drill me. He made me look him in his eyes over, and over, and over again. The overwhelming blueness of each of his irises encouraged me to concentrate beyond any ability that I knew I had. I swam into socialization on the cresting tide of that blueness.
I never knew how to join the conversations of other people. I had a terrible habit of interrupting people in the middle of their sentences whenever I saw a group of people I don't know and I wanted to approach them. I've always been pretty talkative for an introvert - since I finally started talking after a delay of a few years, I've barely stopped for breath. My feelings of anxiety and insecurity in social settings haven't helped - time has always ran fast for me when I'm around lots of people I don't know. I still have trouble finding a way to relax, slow down, and remain patient without disengaging entirely.
Every time someone tells me that they would never know I had Asperger's Syndrome is a victory lap. I have spent so much time and effort trying to be like my peers. Why do I want to identify myself through the prism of a disability, when I'd rather identify myself by the struggle I've undertaken to overcome my condition? Perhaps that's the best reason to self-identify: so I can provide some frame of reference for the sustained campaign I've waged against my own mind to free a little bit more of my soul.
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