Tyran Hawthorn is a student on my course and he had an exhibition in Eldon. The opening night was on Halloween, October 31st, and I thought it would be a good opportunity to see what a gallery opening night should be like. As you walk in you are immediately greeted by a set of A2 images. There is text alongside the images which explains the reason behind the exhibition. Everything is very spacious and in a white cube style exhibition. As you walk further there is a large buffet of delicious looking snacks and drinks. As you can tell from the photo there were quite a few people there.
Tyran was also there himself to answer any questions people may have had and of course for a nice chat. His exhibition dealt with his disease:
"This is an awareness raising exhibition and fundraising charity event for research into Duchenne Muscular Dystrophy, an incurable and terminal disease which causes the decay of muscles and difficulties with breathing and movement.
Tyran Hawthorn uses surreal and experimental photographic images to illustrate his mixed emotions of anger at his condition, juxtaposed with his enjoyment of heavy metal music, horror movies and escapist dreams from everyday life.
This fascinating genre of art that features objects rich in morbid symbolism such as skulls, rotting food, and wilting flowers, which are used in order to produce in the viewer's mind an acute awareness of the brevity of life and the inevitability of death.
Duchenne Muscular Dystrophy otherwise known as (DMD), is a devastating genetic muscle wasting disease which is caused by a missing protein. People sadly infected with this, witness their muscles degenerating throughout their entire lives and eventually leading to paralysis and early death. Families struggle to cope with the diagnosis and day to day management of this condition for which there is no cure, and the only hope for families lies in new treatments that can slow or stop DMD in its tracks.
The majority of the proceedings of my exhibition will be going to a charity known as Action Duchenne. This charity is the only National Charity that exclusively funds research for a cure and promotes campaigns for better medical care for Duchenne Muscular Dystrophy. The essential work that Action Duchenne do is priceless, and I can only hope that my exhibition will take us one step closer to a cure.
When you first get diagnosed with Duchenne, you feel as if you are covered in a shadow of overwhelming emotion as you are given no hope by the doctors. As the arrow of time ticks on, you begin to realise that it is not all 'doom and gloom'. Due to medical advances, you are given a longer life expectancy and with the fight for a cure harder than ever there could be a bright light in sight before the pearly gates. The following statement relates well with this series of work; 'It would seem that photography begins in darkness and death, but ends in light and vision'. 'Disability does not mean inability'. This is my exhibition, this is my work; this is me." (text from his website).
Tyran also had printed quite a few leaflets for his exhibition which we scattered throughout all of Eldon. They were double sided and printed on card. It had his photos on it at well as all the important information. He also had a link for his website to find more information. All in all I found it a very interesting exhibition. He combined both photographical work with a box of the mouldy fruit he photographed which made the exhibition very interesting and unique.