“Autistic Boy” – watch this brilliant film made by an 18 year old autistic highlighting the positives.




Autistic Boy - filmA couple of days ago we were asked by the BBC to share this brilliant new film entitled “Autistic Boy ” made by an 18 year old autistic.

Set in a small office in Birmingham this film documents the positive impact Asperger’s Syndrome brought into everyone’s lives!

Gerard writes “I’m Gerard Groves, I’m 18 years-old, and I love making stuff: films, comedy sketches, project ideas… Basically anything people can watch and enjoy or laugh at or learn from. I’ve been making films since I was a 12 year old kid dressed up as Doctor Who in my back garden; my dream is become a cross between Ridley Scott, J.J. Abrams, and Quentin Tarantino. I’ve just moved from Birmingham to London to start my new job as a BBC Production Apprentice I’d love to hear your feedback/support/criticism/plans-to-take¬-over-the-world!”

Please do share any comments you have about the film in the comments section below.


Life with Aspergers Syndrome, ADHD, Bipolar disorder and Irlen Syndrome- check out the videos of Tom Schofield


TomTheOne

TomTheOne

A few days ago Tom Schofield got in touch to tell us about his YouTube video channel The Tom One.

Tom shares “Hello everyone, I’m Tom and I’m a 26 year old man with Asperger’s Syndrome, ADHD, Bipolar disorder and Irlen Syndrome. I got my first diagnosis when I was five years old and that was ADHD after my primary school said I was too much of a wild child. A few years later at age 8, I was given a diagnosis of Asperger’s Syndrome and finally some accommodations were made for me at school.

At 21 I was dragged to the doctor by my then wife after experiencing extreme mood swings over a period of several months and he diagnosed me with bipolar disorder, then a few years later at 26, I saw a specialist optician after complaining about extreme light sensitivity that had plagued me my whole life, and it had started becoming worse. He told me that I had a form of vision disorder called Irlen Syndrome, a condition that is very common in autistic people, but not exclusive to us. It’s where your eyes function as usual (meaning you can have visual disorders and still have this) but your brain can’t perceive the visual input properly.



I made these videos because I wanted to help people understand autism a little better, and hopefully offer some insight into what it’s like to live with day in and day out. More videos will be done in the future, including some involving some of my friends, who are also autistic.”

He goes on “I made the videos because there was a lot of research done on autism, but hardly any of it was done by autistic people themselves, never mind portrayed it from a perspective that knew how it felt to be in these situations. I got tired of people misunderstanding behaviour from us as bad or strange, when they didn’t understand the reason. I also wanted to help parents understand their autistic children a little better.”

You can watch Tom’s videos which cover such topics as loneliness, eye contact and sensory overload by clicking on this link.

Who coined the term Asperger’s Syndrome? Tributes to Lorna Wing RIP


Dr Lorna Wing who coined the term Asperger's Syndrome

Dr Lorna Wing who coined the term Asperger’s Syndrome

In fact I’ve seen Lorna Wing, the woman who coined the phrase Asperger’s Syndrome, a few times on TV but was unaware of her contribution to the lexicon of the autism community.

Not just that she was also a co-founder of the National Autistic Society (NAS) here in the UK in 1962.

Indeed so important was she that her death a couple of days ago made the new headlines.

Like so many of us in the ASD community it was having a child diagnosed with autism which sparked her interest the subject. I knew nothing about ASD until our son John was diagnosed in 2009.

Not just was Lorna a physician and a psychiatrist she was also a pioneering researcher in the field of autism. While her own daughter could be described has having “classic autism” she took up Has Asperger’s research into autistic children who do not have typical speech disorders as part of their ASD. So giving the now commonly used term Asperger’s Syndrome. She also saw that autism was a spectrum rather than a fixed set of diagnostic criteria.

The aim of this blog post is to collect in one spot a few of the obituaries and tributes to Dr Lorna Wing. For me, at least, she represents the tenacity that it see in so many parents of children with autism.

If you have written a tribute or know of a an obituary please feel free to put a link in the comments box below.

To start the process I’d like to share the UK’s Daily Telegraph obituary which will give you a great overview of Dr Wing’s life and the importance of her work. You can read NAS’s tribute here.

Thanks very much in advance. And thanks Dr Wing!


Life Compass Camp – A specialized camp for Autism, Aspergers, ADHD and Social Anxiety – Read our guest post from Robin Wright


Life Compass Camp

Life Compass Camp

Welcome to the latest in our series of autism guest blog post. Today Robin Wright tells us about Life Compass Club – a specialised camp for people with autism and similar conditions.

Wright shares “We offer our campers (age 7-17) a true summer camp experience filled with fishing, archery, games, and fun, while also catering to their specialized needs. Our philosophy of experiential learning helps them discover team building, leadership, and social skills as well as spotlighting each camper’s unique talents. Our highl trained staff are passionate about our campers and v9lunteer a week of their time to create an amazing experience for everyone. If you would like more information, please visit our website ( http://dunesmorainebsa.wordpress.com/life-compass-camp/ ). Please also help support our mission by liking and sharing our Facebook page, www.facebook.com/lifecompassdaycamp

Life Compass Camp

July 28 – Aug 1 2014

Camp To-Pe-Ne-Bee, Michigan City, Indiana

219-309-4167″


Autism and University Life. In the is guest post Ryan Hendry tells us about the transition to university from the point of view of a person on the autistic spectrum.


Holding Out a Hand

Holding Out a Hand

Welcome to our latest guest blog from a member of the autism community.  Today Ryan Hendry tells us about his transition from school to university as a person on the autism spectrum!

Ryan a 19 year old Law Student at Queen’s University Belfast, and I have Asperger’s Syndrome, which was diagnosed when I was 14. He also runs a group which aims to promote and raise awareness of Autism, Asperger’s and ASD.

You can read Ryan’s blog here http://whatsitliketolivewithautism.com/ or follow him on Facebook at
www.facebook.com/holdingoutahand

Ryan says “For several hundred thousand teenagers every year throughout the UK, the transition from secondary school to university is fairly straightforward. But for a number of people on the spectrum like me, the process can be anything but.

The difference in styles between school and university is enormous. From the timetabling of classes to the way classes are structured, everything seems to be different. As an 18 year-old leaving school education for the first time in my life it seemed terrifying because of the sheer number of changes I’d have to face.

One of my biggest fears was that the support that Queen’s University would provide me was going

Autism Awareness at University

Autism Awareness at University

to be a standard “box-ticking” type that would not be sufficient in order to allow me to cope with the change. However, at the end of July, the university asked me to attend their offices one day, in order to allow for an assessment of my condition. This was a very straightforward process and allowed the university to tailor the support that was to be provided to my exact needs, much to my relief.

My current support is much the same as it was in school. I have a note-taker that attends all my lectures and tutorial classes, and it helps me not to worry about being unsure of what parts of a lecture to note down, as well as providing a consistent style of presentation for the notes, helping me to keep them organised. The support provided during exams is also largely the same: I’m given extra time, separate invigilation, a computer to complete the exams on, and rest breaks if needed at set intervals. This continuation of support was a huge help in helping me settle in.

Facing my fears

The next big step is the change in scale from school. In my school, our classes had, on average, 20 to 25 people in them. In university, my lectures can have upwards of 200 people in the room at one time. As someone who has always had a fear of big crowds, this was particularly concerning to me. However, I found that although the number at first sounds very large, the lecture theatre that our lectures were held in was larger still, which allowed the crowd to spread out, helping to ease my fear of being squeezed into a room with 200 other people. For tutorial classes, these usually contain around 15 to 20 people and are quite close in style to classes in school so these did not represent a substantial concern for me.


My biggest fear was the reaction of other people. I had sometimes been bullied at my secondary school and although it had completely stopped by the time I started my sixth year, the fear started to creep back in when university loomed. The fear was less about being bullied, and more about being left out of the group and not being able to make any friends. I was also worried about the reaction of the other students when they would begin to notice something a little bit different about me. Would they be sympathetic? Would they be understanding? Or would they be ignorant to the problem? This concern continued over the course of the summer and, despite frequent attempts by my family and friends to persuade me otherwise, the fear never went away.

Settling in

The first day at university was terrifying until I attended the induction day that had been set up by the University. This was an extremely helpful day for me, as it helped me to feel a bit more comfortable. I realised that many other people were in the same position as me, starting a new part of their education, in a new place with new people. The fact that we all had shared interests allowed us to have a common subject to talk about and get to know each other about.

My experiences with other students have been particularly encouraging for me. I wear a wristband, that says Autism Awareness on it, and one of my friends happened to notice it and asked what it was about. I explained to her about my condition, and that I had set up a group to try and help other people overcome the same obstacles that I was now facing. This was the true test for me, as I had no idea what the reaction was going to be, or whether I should even tell anyone. Her reaction was one of slight shock and she said that she only understood a little bit about autism. She also asked me if I wanted her to try and let other people she knew about my condition, in such a way that it wouldn’t come as much of a shock to people, which did encourage me. The overwhelming reaction of most people to the news of me having autism is one of slight surprise, which quickly turns to understanding and also an interest in gaining a bigger understanding of the condition.

Adapting to my new life
Even with all these positives, it still did take some time to get used to the change, and I knew that it was always going to be a struggle at the start to get into the ways of life at university. I will admit the first few weeks were a huge battle, as for the first time in my life I was expected to buy my own textbooks and basically build my own timetable, in order to allow myself to complete my work on time and to an acceptable standard. This did take a few months to get used to, but I knew that eventually I would get it. There were a few hard days, and some meltdowns as the stress built up at times, but by the time Christmas had arrived I found myself in a good routine and starting to fit comfortably into the life of a student. There is the occasional day that I do have a struggle, or something doesn’t go the way I expected it to, but I try and learn from these in order to deal with the situation better the next time around. The support my friends have provided me with on the bad days has been very helpful. They keep telling me that everyone has bad days, not just me.

Looking back now, the decision to go to university has had an enormous effect on me, and it has allowed me to do things I never thought I was capable of. It has improved my confidence dramatically and I now feel at ease with being able to do the tasks that others find second-nature, such as buying my own train ticket, going for lunch with friends, going to the library to study, and being able to plan my own day has given me an amazing sense of freedom. As well as this, just recently I finally overcame one of my biggest fears, public speaking, by giving a talk to a group of teenagers who have autism. Although the group only consisted of a dozen people, it was something that I previously would never have even considered doing, but thanks to the confidence my experience at university has given me, I was able to do it, and according to the person in charge of the group, they said it was an excellent talk.