LUZ LOZANO PEREZ

Fathers and mothers from all over Spain, aware of the seriousness of our children, we decided to fight to give them a better and hopeful future. That is why we have joined together in order to raise funds through the Duchenne Parent Project for research. Currently we have launched 22 research projects in our country aimed at finding a cure or improvement for this disease. Help us to follow, JOIN OUR CHALLENGE! desafioduchenne.org

Hi! I'm Aitor and I'm almost 10 years old. When I was 2 years old, I choked on a sausage and got very sick. I went into cardiorespiratory arrest for more than 15 minutes and with a lack of oxygen to the brain. Now it's as if I had new one month, my little head has been damaged and I need help for everything, I can't see, talk, or move, I need a very expensive neurorehabilitation treatment and something else that I can't have, if you help me I promise to give you a smile.

La Fondazione Alba Pérez combatte contro il cancro infantile. Il sogno di Alba, un sogno che può diventare realtà. Insieme abbiamo ottenuto molto, abbiamo condotto un'indagine sul cancro infantile, insieme abbiamo formato una grande famiglia di Teaming che combatte per i sogni di Alba che sono molti, ma il principale è trovare una medicina contro il cancro infantile. AIUTACI CON UN SOLO UN EURO UN MESE.

Las NEUROFIBROMATOSIS son un grupo de enfermedades raras originadas por una alteración genética que provoca en los afectados un crecimiento descontrolado de tumores en casi todo el organismo. Hoy en día no tiene cura. Desde la Asociación damos todas las pautas necesarias al afectado y familia, que incluyen información, orientación y apoyo. Trabajamos para lograr un fortalecimiento de todos los aspectos psicológicos y sociales y lo hacemos de una manera profesional.