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People can participate in AlbinosChile.cl until December 3
There is a series of myths about the albino community that they see better at night, that they can not
The condition caused by the lack of pigments in the skin, hair and eyes carries so many stereotypes and myths that in Africa the albino children are hunted by bone merchants because they would have magical and healing qualities.
In Argentina, a few years ago, the albino community was organized by social networks to pbad a bill ending the limitations. and restrictions of daily life.
In an attempt to put an end to these problems affecting about 1000 citizens in our country, Corporación Albinos Chile decided to record the amount of people with this disease and thus inform the people of their reality . People can participate in AlbinosChile.cl until December 3.
In an interview with Emol, the president of the organization, Claudia Núñez, explained the reason for her idea of counting Chilean albinos for the period . ] demolish the prejudices and apprehensions that exist about them.
According to Núñez, the lack of information affects albinos since their birth. The parents of the children themselves "become very stressed" because many times doctors do not have enough knowledge and end up frightening and confusing families . "There are doctors who come to tell the parents that their child is going to be almost blind and that it is not true, so imagine the impact that it generates." Some even derive it from the neurologist, saying that it's not necessary, "he said.
Later, when they are children, they are exposed to a series of prejudices because of their appearance, which often are not intended for malicious use, they have an impact on their design. "Angelito" or even "the eyes of the devil" are some of the observations that people make when they see them.
In terms of work, there is also a lack of opportunities for the albino community. "You can have a doctorate and, if you are applying, it is highly likely that they will choose one who is not albino because they do not know that an albino needs one. computer as another and he will see how he enlarges the letter, and he will be able to do like everyone else, "explained the president of Albinos Chile.
The organization plans to solicit funds to fund projects that allow society to be informed about what it means to be albinos and to create support networks for parents of children with albinism. In addition, Nuñez emphasized the importance of specially training health professionals, parents and educational communities .
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