Teatrabilità Being able to communicate, thrilling and moving, and then give what has been built for those who want to see him. On the way we had a transformation, in a group of people who feel free to express themselves with their own skills and their own limits without feeling judged or judge, so we pulled out of our desire to live and let out our lines, thoughts, emotions beyond the label of disabled people, disabled, fearful, distressed, disturbed, strange, that it is exaggerated. Parents realize the quantum leap of their children who are freed from the shackles of the symbol, and feel free to be people with a disability but who do not have it? And so we do not give importance to disability but to the expression of themselves, for example, there is the cliché of down that are sweet, affectionate and cute .. but this is characteristic of Down syndrome or characteristic of that person with his experience of life?
You think too much on the symptom, the syndrome, and there is the problem too little space for the person, we want to address the superficiality of bars ... the boys with Down syndrome are also aggressive, tired, angry not to be accepted, not understood except with fake hugs is a charitable ... girl who was locked up in itself and through teatrabilità was allowed to play his rage and also his passion of love is unleashed ... and I say it? We here at the theater ... and the recitation of themselves ... .. and she commented: "I'm being attacked, do not let me live, I want to live!
I love the theater! When we are awake from the sleep of banality we can learn playing or creating.
The theater is half of my life, you learn growing up with the group and then be ready to go in the world as individuals ..
I am disabled, I am olly
and his mother comments: "The first response that I think about the many opportunities, clear and almost obvious that he met Mb attending your group: the heat a friendship continued for many years, feeling the protagonist, a set of players, not being forced to use his usual defense of automatism, in response to the fear of demands are too high, the opportunity to express its resources and potentials, knowing that it will be appreciated. All this certainly makes her feel at home, free.
What is more, and this directly affects me and the abstract image of an ideal daughter who has always guided my relationship with Mb, the image of "My Daughter", which appeared and appeared, however, , as close as possible to normal.
For years I tried to build a dummy, suitable for being in the world, so fair, so, in fact, normal. But when did I fight with Olli, dancing, happy, all his charm and his love
or the singer of "Song alien, that makes the strings vibrate deepest of despair, which brings in for a lifetime, then I realize that, despite myself and despite my models, the most genuine, spontaneous and true to Mb is still alive, ready to open up and cry out his desire to be there.
's so that the teatrabilità gives, finally, on the Mb opportunities to be herself,
to be, in fact, Olli. "
Then a meeting in town for a coffee on a design that has created the "Sun" which has divided the disabled from the disabled and normal and developing a dialogue and reflection on September 20th Avenue with teenagers sitting on the benches they were doing chaos by passing the time said:
"in the world there are disabled, and are divided into less down, down, serious, substantial down, then people with disabilities who are physically handicapped, wheelchair, blind, dumb, deaf, crutches, etc. .. otherwise healthy and who are so skilled that unnecessarily drive me crazy, I do not feel understood, I do not feel free to live "
And children with communication difficulties and relationship because of other syndromes such as Williams have made them stop mentally experts say a 8 / 9 years but their life experience has made them learn other things, whether the brain has stopped does not mean that everything the brain has stopped, but only a part (call it cognitive) but ... part of the experience, that report was very active but no one believes and continues to consider them only for their syndrome without him nor trust nor responsibility while watching a movie on TV where the main character is alone and no one believes (as in the end he will have been right) says: "It's like me!" in what sense? I ask, because no one believes him, like me, nobody ever believes in what I say. "The teatrabilità gave him the opportunity to speak and he pulled through the ability to mimic what brings out his emotions, has given the confidence he lacked, or other persons designated sad, socially maladjusted that sun and say, "Teatrabilità is an opportunity, how, as an opportunity to express themselves, but everyone has the capacity to shyness or lack of opportunities experienced a bit 'in hibernation, there lies, or asleep, or things resulting in a form of repressed anger.
I am shy, but apparently did not appear and are definitely not used to being so open with people so I get used to the way of being of others, I do drag, I believe more in myself, I love the theater and I love to express myself for who I am, I feel that this group is for the opportunity to train me to be myself. "
You can not explain what we can only do it live, not a business, is through the instrument activities (dance, song, mime, dance, poetry, interactive games, etc..) are given the opportunity to be themselves starting from what one is at that moment was his way of speaking at that time, to release what we have in and keep him for the chosen few, and too often people have no elected different labels that they can trust.
There is so much support and too little education. To educate
must first have the courage to go beyond labels and into the boy who is in every one of us.