Little Cauliflower Theatre
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Production Week 

29/7/2013

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Wow! The last few weeks have been crazy! We performed at Marlowe Theatre Scratch Night in Canterbury and then went off to Kingston for our residency with Creative Youth at the International Youth Arts Festival. After three nights of work-in-progress performances, we want to share some images and audience feedback. 

More information will be posted here soon when we have completed our Arts Council Evaluation. 



FEEDBACK
Do you think that we dealt with the subject matter appropriately? Please explain.

"I felt it was very sensitively dealt with. Ted was portrayed beautifully with the right measures of humour and heart". 

"Yes, you seem to have a clear understanding of MND". 


"It’s crucial to highlight the positive attitude to an awful situation. You brought out Ted’s perseverance and positivity beautifully".

"Yes, I thought it was handled very delicately - it enlightened me to what MND is and what that could mean to someone".

Did the different styles of puppetry (full bodied Ted, the head and hand and the shadows) compliment or distract from the narrative? Please explain.


"Really enjoyed the variety. Thought some of the shadow puppetry was brilliant".


"Really enjoyed the variety. Thought some of the shadow puppetry was brilliant".


"Complemented, not sure whether they could blend better".


"Found the shadow puppetry stunning and very beautiful - perhaps the lighting behind was slightly too bright (could see the strings quite easily at times)". 


What do you think we could improve on?


"Some of the shadow figures could be slightly larger". 


"Ted’s relationships with his goldfish and lady were lovely, I almost wanted to see more of his story/narrative and less about the disease (which is still very relevant) I wanted to see more of Ted pre-MND to really connect with him".

"If there is a reason for all the little boxes for the props, make that clearer". 



"Transitions - make breathing a stylised choice and more of it to the music". 


"Explore the relationship between the couple more".

"Maybe we could find out more about the disease"?



"A tiny detail; when you are doing the puppeteering behind the screen it would be good to have your feet fully covered in black as not to distract the eye". 


Many thanks to all who share their thoughts and feedback. It has been greatly appreciated.




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Marlowe Studio
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Feedback Day at Canterbury's famous Beano Cafe!
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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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