Baby born without a nose, manages to surprise, going beyond the doctors' predictions

This is the story of a bimbo to whom life has not given a long or easy path. After his death, his parents tell the story of their brave little man.

Eli Thompson
credit: Jeremy Finch's Facebook with his late son Eli Thompson

The small Eli Thompson comes into the world on March 4, 2015. His appearance from the first moment of life caused a sensation. The reason is simple, little Eli was born with a rare disease called arina.

THEarina it involves a deformation of the face and the total absence of the nose and nasal cavities. As soon as the baby was born, he was rushed to the hospital Children's and Women's Hospital, in a specialized pediatric ward, where he was given an emergency tracheostomy to help him survive.

The urine from which little Eli suffered was total, so that not only did he not have a nose, but also no nostrils. For doctors it was necessary operate urgently to recreate the nose and make holes in the jaw to allow air to enter and exit.

The little boy flies to the sky

Unfortunately Eli, despite his will to live and tenacity, didn't make it and died shortly after 2 years from birth. The child, just in that period had given much hope, was beginning to learn sign language and to say something with the help of the speech therapist.

Precisely because of these improvements the parents cannot explain why the child died.

There is nothing more atrocious than pain for the loss of a child, an event so dramatic and unnatural that it interrupts and changes the life of the parents forever.

Little Eli with his tenacity and his will subverted the predictions of the doctors, who would never have believed that he could live with such a serious pathology. The child will now give his wonderful smile to the angels and will continue to live in the hearts of his parents and those who loved him.