The 16 years had a normal as any girl until last October. From there her breasts began to grow disproportionately. The size from 38 to 50 and bra seemed to fit right.
Silvia Puentes, mother, moved from emergency to a medical facility, but the doctors ruled out any abnormality. “It’s normal,” he said in his time.
Yesica, a senior bachelor’s degree in Higher Technical College does not support the weight of his two ‘tits’ and a spinal pain that daily attacks that threaten to divert their small body forward.
“Suffer greatly. It is not good bra, and not get one of its size anywhere. Then I have to forward them with clean pieces of cloth under it to machine because there is no choice. The strips will not sell, less glasses, “says Sylvia, who explains that the problem is not genetic because his family is slightly raised breasts.
“I took her to a gynecologist, he did an ultrasound, but everything went well, nothing evil. Still, her breasts continued to grow. The doctor asked me to make her lose weight, but she is so fat,” says the mother , who, seeing the disparity decided to change the specialist, who recommended a reduction mammoplasty, a surgery for breast completely destroy and reconstruct others.
And then began the ordeal of Bridges Mejia. Specialists in plastic surgery and gynecology insist Yesica operate as soon as possible but bureaucratic delays health services have prevented it.
“It is deformed, we make a medical board meeting with other experts in the field,” advised the doctor Jose Ignacio Tovar, a plastic surgeon, who championed the issue in Hernando Moncaleano Hospital of Neiva, the maximum neivanos care center.
“They are like having masses in the breasts are not malignant, there is no threat of cancer. What if the doctor told me is that you grow more if we do not care,” says Silvia disconsolate.
In the closet are abandoned Yesica blouses and bras are the same fate. With its unusual size, things changed and low-income family had no choice but to break the sow (piggy bank) of the savings and buy four shirts and two pieces of fabric to the support arm him. “He only has two, one that is removed and another put because they do not get. With the school uniform will be a drama.”
The disease is called gigantomastia
Yesica Johana start studying next week and since already said it intends to cripple their classrooms.
“It’s very hard, I am different. I never was sick, began to grow slowly and then very quickly, I still rising. If you go out anywhere around the world looks at it, start talking about one and laugh at my breasts,” says the girl with a very soft voice of a girl of that age.
“I have a boyfriend and is in the army. He does not want me because it is dangerous to operate and loves me well,” he says while calling a chair to sit because he feels exhausted. “When I sleep I can only do it face up, face down is impossible,” he says.
Jose Ignacio Tovar, specialist in plastic surgery ELMUNDO.es assured that the disease is gigantomastia couple, a nervous system disorder produced in very few cases in pregnant women.
“They are not recorded frequently in children. The surgery is complicated, but we are going to do because it deserves to be well. After surgery guarantee an improvement of 90%,” explained the specialist who added that when you have to breastfeed children.
Yesica Johana complex live with as they decide to enter an operating room and take off the weight that loads under my belt for some women become sex symbol, while for others a veritable ordeal which will not return ever know.