Home » PALATOSCHISIS MALFORMATION DAUGHTER GIANLUCA VACCHI / “Bone fragments to rebuild …”

PALATOSCHISIS MALFORMATION DAUGHTER GIANLUCA VACCHI / “Bone fragments to rebuild …”

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PALATOSCHISIS MALFORMATION DAUGHTER GIANLUCA VACCHI / “Bone fragments to rebuild …”

PALATOSCHISIS MALFORMATION DAUGHTER GIANLUCA VACCHI: THE WORDS OF THE ENTREPRENEUR

The little daughter of Sharon Fonseca e Gianluca Vacchi as soon as she was born she encountered a problem in her palate, the cleft palate: “A health problem, clearly there are much more serious things, this was a solvable thing, but a child’s problem is never a routine problem. Our daughter was given 25 points on the palate in a mouth the size of two coins, so they had to reconstruct with bone fragments, ”commented Gianluca.

“When they told me I was about to lose consciousness,” admitted Vacchi, who preferred to include this aspect in their documentary as well. The entrepreneur wanted to thank the surgeon of the Parma hospital who operated on his baby, Blu Jerusalem: “It was extraordinary,” he admitted. (adj. by Emanuela Longo)

PALATOSCHISIS, MALFORMATION OF THE DAUGHTER OF GIANLUCA VACCHI: WHAT IT IS AND HOW IT IS TREATED

The cleft palate it is the disease on the palate of the mouth that has affected Blu Jerusalem, the daughter of the well-known entrepreneur Gianluca Vacchi, and companion Sharon Fonseca. It’s about a congenital malformationwhich therefore appears from birth, and which affects the soft and / or hard palate, then causing a crack that can be of variable size in the hard palate. It is one of the most common congenital anomalies in that area of ​​the body (usually affects one in a thousand), and can involve difficulties in sucking breast milk but also in eating, therefore problems in speaking, in the teeth, and also predisposition to otitis of the middle ear. The problem with cleft palate is that it is the same is hardly identifiable before birth, while once the baby comes into the world the recognition is immediate, and requires a simple examination.

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Fortunately it is easily treatable with excellent results, and the main treatment is surgical type: an operation is carried out to close the crack that occurs on the palate. Often and willingly those who suffer from cleft palate have to undergo various interventions throughout their life up to the age of 18, and the first operation is expected between the sixth and twelfth month of life. Subsequently, after several years, usually in adolescence / late adolescence, we intervene with the aim of perfecting the appearance of the palate and adjacent structures. Obviously, everything is linked to the type of case and when the intervention is performed for the first time (the intervention is recommended no later than 18 months).

PALATOSCHISIS, MALFORMATION OF THE DAUGHTER OF GIANLUCA VACCHI: THE MESSAGE FROM THE ENTREPRENEUR AFTER THE OPERATION

Gianluca Vacchi and Sharon Fonseca have decided to have their daughter undergo cleft palate surgery last April 2021, exactly in the sixth month of his birth, and on the occasion the well-known entrepreneur and influencer had published a moving shot from the hospital with his little girl in his arms, and bloody shirt, in which he wrote: “On Monday, our little Blue Angel was operated on to correct her congenital cleft palate. These have been very difficult days, seeing an innocent creature suffer is a very trying experience. She, with her sweetness and her strength, went through this storm with the calm and strength that God has endowed her with. I am proud to be his father and I will never wash the shirt with his blood from the first post-operative hours in which my arms were his only certainty … I want every internal and external memory of this profound lesson of courage that this little angel has to remain given to me and Sharon ”.

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