program good night family [Eltrecce]lived one of his most emotional moments. leo and thiagotwo five-year-old twins suffering from Noonan-Lasopathy Syndrome become the protagonists of a story that touches everyone’s heart. It was the idea of Nico, a close family friend, and we decided to star in a cycle led by him. Guido Cachuca Help improve their quality of life.
The small children we take care of every month. Garrahan Hospitalyou will need to travel from Escobar to the medical center in Constitución. However, his family’s financial difficulties make traveling by train and bus increasingly complicated. Moved by this reality, Nico proposed the following romantic cumbia show: Leo Mattioli And the whole studio collaborated on it.
During the broadcast, a video of the twins gently introducing themselves to the viewers was shown.My name is Leo. My name is Thiago. We are twins with a syndrome called Noonan Lasopathy. We are 5 years old and patients at Garrahan Hospital. Sometimes you can’t travel because you don’t have a ticket. When I go there, I go by bus and train. “We are very funny,” they said with a smile.
The impact was immediate, as in just 15 minutes of the program, the public donated P25 million to help families with medical and transportation costs. On social networks, hundreds of users praised the gesture of solidarity and left loving messages. “Guido, you are an angel to those who need it most”, “Beautiful twins, I follow you on TikTok” and “Thank you for helping them, they make us happy every day.”were some of the most repeated comments.
Thiago and Leonel’s case attracted attention not only because of their kindness and the difficult economic situation their family is experiencing, but also because of the medical conditions they both suffer from. Noonan syndrome is a rare genetic disease that affects the normal development of the body and manifests in a variety of ways.
According to information from the Mayo Clinic’s professional portal, the condition can cause certain facial features, short stature, heart disease, and certain developmental delays such as walking, speaking, eating, and learning new skills.
Its origin is related to dominantly transmitted genetic changes. This means that it is sufficient for either parent to inherit it. However, in many cases, the syndrome develops due to a spontaneous mutation without a family history.
There is no definitive cure, but treatment focuses on monitoring symptoms and preventing future complications. In some patients, doctors may use growth hormone to increase height and stimulate growth. Each case requires continued monitoring, as the twins have been receiving since their birth at Garrahan Hospital.