BREAKING THE STIGMA
This report aims to bring the Acondroplasy, short stature or dwarfism commonly bone, a public that has not ever wondered that it is in fact to all who see and look at him rarity.
To stop feeling those prying eyes burlesque and break the stigma, the protagonists show us their personality, their hobbies and their surroundings, their struggle. A fight face to face with a disability lasts, where they face all the difficulties they have to accept and fight, imagine in advance all the problems that arise can be as hard. The role of parents and family is very intimate importantly, they also face a big challenge, bring and defend all normal and strength as possible to the child to feel secure but not overprotected.
This constant monitoring is essential to avoid problems in the development of the child, and keep in contact with other co-operated, chat with them and watch them closer to reality to lose their fear of the operation, the relationship between them is the confidence to continue improving the process of lengthening dee warm.
Today, many boys and girls between 10 and 14 years face harsh force operations with an adult, with a hopeful illusion to narrow their differences, this is their little big target, reducing their abnormality inches. Their fears, dreams and desires are based on those inches, that will lead to a better adjustment to now they have and improve their self-esteem. Without expecting anything in return, only the respect of others.
The importance of these centimeters is very different in our thinking, that in his, we can not conceive of this importance, we think too much sacrifice for so little, but in their eyes is a new life, this small difference the brand in many everyday acts, such as calling the intercom of his friends, the elevator, here as if it matters to have independence.