Little Cauliflower Theatre
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DAY 3 - Canterbury

22/4/2013

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Will
It was our first day rehearsing down in Canterbury as a collaborative today. We spent most of the day discussing the background and personality of our protagonist.

'He' is a solitary man who's let life carry him along with no real ambitions until now. He has a chair, and possible a pet fish (a Blackmoore), oh, and he likes trains. We think he has a brother, but no wife. A job, but no career. And, most importantly, an extraordinary imagination. 

Questions we are hoping to answer this week are:
  • How does he react when he is first diagnosed with MND?
  • Who does he tell?
  • How does it change his outlook on life?

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    Little Cauliflower 
    & 
    Smoking Apples

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    This is a blog dedicated to our Research and Development of CELL, an exploration of Motor Neurons Disease through puppetry and visual theatre.
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    www.smokingapplestheatre.com
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    www.redthreaders.com
    " MND is a progressive neurodegenerative disease that attacks the upper and lower motor neurones. "
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    "In my view, mental and physical aspects of MND go hand in glove - if one has the right frame of mind, one can almost achieve the impossible"
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    " I'm living with MND, not dying from it. "
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    " I first saw the task as one of preserving my personality, of showing the world that my mind has not gone down the tubes with my voice. If I cannot say as much as I used to say, I have to say it better. So the choice of words becomes crucial. "
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    "  He accepts life and works on the process of fate. What if life no longer accepts you?  "
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    "  Initial symptoms are: frequently yawning, deterioration of speech, tripping and unexpectedly dropping things.  "
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    " I might be unlucky having MND but I think I am blessed to have the family that I have behind me. " 
    Mark Maddox
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    "I have had  motor neurone disease for practically all my adult life. Yet  it has not  prevented me from having a very attractive family, and being  successful in my  work. This is thanks to the help I have received from Jane, my children, and a  large number of other people and organisations. I have been  lucky, that my  condition has progressed more slowly than is often the case. But it shows that  one need not lose hope."
    Stephen Hawking 
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     " It’s hard because I can’t even play football with the kids and I can’t do stuff that you normally do with young children." Mark Maddox
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    "It's been said that the care and support you receive is a bit of a postcode lottery but in my two-year journey I've met a lot of kindhearted people."

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