MONTSE SANCHEZ CAMACHO

A los 5 años me diagnosticaron el síndrome de sanfilippo.Una enfermedad rara. Desde los 15 años a los 20 ya no he hablado, ni sonreido, ni caminado , he sufrido epilepsias , ceguera y en 2023 fallecí. Mi madre con su dolor sigue trabajando por los niños que como yo sufren el sindrome de sanfilippo.Si quieres + información, siguenos en nuestras redes sociales. Sanfilippo Barcelona. Un dia desde el cielo,estaré feliz al ver que mi madre consiguió una cura para el resto de niños.

Non-profit non-governmental association, created by civilians and personnel of the state security forces and bodies, armed forces and emergencies to ensure the needs of sick or troubled children, visiting them in hospitals, shelters, NO CHILD NO SMILE, with your euro a month you can help us get it. EVERYTHING RAISED WILL ABSOLUTELY GO TO CHILDHOOD PROJECTS AND NEEDS www.asociacionsonrisas.org

Ajudamos mais de milhares de causas sociais a tornar os seus projetos possíveis todos os dias. Desde que lançámos o Teaming, já angariámos mais de 50 milhões de euros para as causas, totalmente livres de comissões. Criámos este Grupo Teaming para ajudar a Fundação Teaming a continuar a ajudar os outros com esta plataforma. Entre outros apoios, graças aos Teamers deste Grupo, o Teaming é totalmente gratuito. O nosso sonho: sermos autossustentáveis graças a este Grupo. Gostarias de te juntares a nós?

I'm Martin, they call me Tintin, I'm 2 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.