In July of 1998 after much relief I found myself diagnosed as having residual Asperger Syndrome by Dr Tony Attwood. I have often been asked what it was like to have been diagnosed. At the time I was 25 years old, I was a student at university with my face hidden behind a bushy beard. I struggled with trying to fit in. I also found life in Armidale almost impossible as I couldn't make any friends or be properly understood by others. I resorted to joining the Masonic lodge as I felt this was a means of finding support and encouragement but instead, I found that I was even misunderstood in it. I was the youngest man in the area to be initiated in the latter part of the C20th. On my initiation which I learnt off by heart, and with the assistance of a short and elderly Austrian/Italian who experienced life in the war, I was able to be duly raised. I no longer am in the Freemasons having resigned some years ago. I never really knew who I was at the time.
Up until I was 25 life seemed confusing to me. I never really knew who I was and more importantly how to get on with others around me. I struggled with depression lot and had thoughts at times about wanting to take my own life. However an inner voice kept me strong and I was determined to finish university no matter what it took. However having a difficulty with reading and undertaking group assessment tasks, I found myself visualising what was required with imaginary participants in order to get through.
Now to the most important part. What was being diagnosed like? Well to begin with it was liberating for in the years prior nobody could put their finger including myself on what it was that made me who I am. I don't want to say what was wrong with me but more so why I behaved and functioned as the person I was and now am. I discussed with Tony my who life's experiences and the current situations I confronted. I described my bouts of depression, my struggles with friendships and my difficulties with socialising and adhering to the requirements of university. I also discussed my earlier experiences of being bullied at school. I also mentioned my desire for friendships also. It is hard to actually go back and describe in detail what diagnosis was like but all I can say is that it helped me and those around me to understand my own internal wiring.
I wrote some poems and short stories but never struck up the motivation to write a book which I did in 2011. I just had to tell the world what life was like as an Aspie and more importantly the struggles I faced. I self published the book as publishers like Jessica Kingsley and other publishers were not interested. So I thought I would just self publish myself. A lot of effort is required to write a book which I was able to do in a week and later have a book launch.
Diagnosis was like stepping in a time machine back to the periods in your life when unanswered questions remained and people's reactions foreign but it appears that the only way forward is to try and use so many coats of paint to try and polish your own image so that you can better adapt to the world. Diagnosis is a means of relief and not a crutch.
Up until I was 25 life seemed confusing to me. I never really knew who I was and more importantly how to get on with others around me. I struggled with depression lot and had thoughts at times about wanting to take my own life. However an inner voice kept me strong and I was determined to finish university no matter what it took. However having a difficulty with reading and undertaking group assessment tasks, I found myself visualising what was required with imaginary participants in order to get through.
Now to the most important part. What was being diagnosed like? Well to begin with it was liberating for in the years prior nobody could put their finger including myself on what it was that made me who I am. I don't want to say what was wrong with me but more so why I behaved and functioned as the person I was and now am. I discussed with Tony my who life's experiences and the current situations I confronted. I described my bouts of depression, my struggles with friendships and my difficulties with socialising and adhering to the requirements of university. I also discussed my earlier experiences of being bullied at school. I also mentioned my desire for friendships also. It is hard to actually go back and describe in detail what diagnosis was like but all I can say is that it helped me and those around me to understand my own internal wiring.
I wrote some poems and short stories but never struck up the motivation to write a book which I did in 2011. I just had to tell the world what life was like as an Aspie and more importantly the struggles I faced. I self published the book as publishers like Jessica Kingsley and other publishers were not interested. So I thought I would just self publish myself. A lot of effort is required to write a book which I was able to do in a week and later have a book launch.
Diagnosis was like stepping in a time machine back to the periods in your life when unanswered questions remained and people's reactions foreign but it appears that the only way forward is to try and use so many coats of paint to try and polish your own image so that you can better adapt to the world. Diagnosis is a means of relief and not a crutch.
