Little Cauliflower Theatre
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DAY 13- The Long To-Do List

13/5/2013

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Carly
Well, what a day. The morning was spent trying to finish our building jobs. When we met at the Rose Theatre at 1.30pm, we had a puppet body, a table, a chair and importantly, a puppet head which we are feeling pretty pleased with.

The rest of the afternoon was spent addressing problems and issues we had with the puppet itself and how we would use it on Tuesday at the scratch. There was a lot of deliberation, running around Primark, BHS and M&S, foam cutting and coffee drinking, but we got there in the end with a long to-do list and left the building at 7pm to go away and do our tasks. We reconvene tomorrow at 10am where I will lead a practical session until 3pm with our work-in-progress puppet.




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    Little Cauliflower 
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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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    " MND is a progressive neurodegenerative disease that attacks the upper and lower motor neurones. "
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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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    "  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. " 
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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."
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