My Child Needs Help Born Unable To Swallow

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My Child Needs Help Born Unable To Swallow

6-2-2020

I WAS BORN WITHOUT SWALLOWING …. ESOPHAGUS ATRESA

Verito Piñan Torres is organizing this fundraiser.

My 2-year-old daughter who was born with a disease considered catastrophic and rare since 3,500 children 1 is born with this birth pathology that is detected after birth,

this condition does not allow them to swallow since their esophagus is not connected to their stomach.

Her esophagus was corrected on the 4th day of birth. It was not immediately because the surgeon works in a private hospital outside the city where we live 2 hours away, fortunately, the surgery was a success and they managed to join Los Cabos of her esophagus.

Unfortunately, this disease involves and manifests itself with other problems that were detected with medical studies by means of an esophagogram such as Gastroesophageal Reflux, Stenosis in the area of ​​surgery and Respiratory Complications such as Pneumonia, broncho-aspirations, bronchiolitis, synovial symptoms, and bronchopneumonia in its 2 years of life has had 8 hospitalizations that have been overcome and a dilatation of the stenosis in the operating room and under anesthesia, so you can eat without difficulty.

In order to have health, we have had to pay for private medical expenses because, for public attention and social security, we have not found specialists who can attend to their medical emergencies.
He is currently a patient in a private hospital and has a medical team such as Surgeon, Gastroenterologist, Pulmonologist, Physiotherapists and their Emergency Pediatricians.

Solving these expenses monthly is expensive since we have sold goods and activities have been carried out to raise funds

FOR THIS REASON, WE GO TO SENCIBILIZE YOUR HEART AND THAT CAN HELP US TO WIN THIS BATTLE THAT LIFE HAS GIVEN US …..

IT IS A WONDERFUL GIRL AND IT IS ALL A WAR IN THE PREVIOUS WE THANK YOUR HELP AND LIFE WILL REWARD YOU FOR YOUR HELP.