Sandra Dí
Toledo, Spanien
Teamer in 2 Gruppen
Spendet jeden Monat: 2 € für 2 Gruppen
Seit 16-03-2023 gespendet: 47 €
Mitglied in folgenden Gruppen
8.886 € Gespendet
283 Teamer
Teamer seit: 16/03/2023
I'm Martin, they call me Tintin, I'm 4 years old. I was born with some malformations and one of them was a cleft lip, for which they operated on me when I was 3 months old. They had given my parents full assurance that it would be a simple operation, but something went wrong and I ended up in the Ucip with mechanical ventilation and deep sedation, and one day, they accidentally extubate me and I went into cardiorespiratory arrest for 15 min, and because of that accident I have cerebral palsy.
2.698 € Gespendet
49 Teamer
Teamer seit: 28/09/2024
El síndrome asociado al SATB2 es una condición genética que ocurre en el brazo largo del cromosoma 2, siendo la mutación o la falta de este gen la causa más común. Las personas con síndrome SATB2 suelen tener las siguientes características en mayor o menor grado: retraso cognitivo, nulo o escaso lenguaje verbal, problemas dentales (macrodoncia o agenesia), fisura palatina, hipotonía, problemas de comportamiento y sueño, epilepsia, osteopenia.