Ofir Arad

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

Somos una asociación sin ánimo de lucro, formada por padres y amigos de niños con distrofia muscular de Duchenne o Becker. Nuestra misión es recaudar fondos para la investigación, tratamiento y manejo de ambas enfermedades. Toda la recaudación irá destinada a proyectos de la Unidad de Patologías Neuromusculares del Hospital Sant Joan de Déu de Barcelona.

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?

This group has been established by Monika to support the school with currently 700 children and to ensure their education. It is our dream goal to get at least 3000 teamers, who would create a monthly financial base. As teamer you can contribute with the value of only one coffee less a month to help the children coming from one of the lowest social classes in India and create a brighter future for them.

Abril is a 7-year-old girl diagnosed with SPG52, with only 50 diagnoses in the world. SPG52 is an ultra-rare disease that causes very serious symptoms such as severe intellectual disability, epileptic seizures and very rapid muscle degradation in the lower body. Abril started walking when she was 3 years old and now at 7 she can hardly move anymore.

Ainara nació el 21 de noviembre de 2015, a las 10:03h. Pesó 1,030kg. Estuvo a punto de morir 2 veces y tuvo que pasar sus primeros 5 meses de vida en el hospital. Ainara tiene atrofia cerebral, epilepsia, hipotiroidismo, hipotonia (falta de tono muscular), su cuerpo no fabrica cortisol ni hormona del crecimiento y padece un retraso psicomotor severo. Ainara realiza fisioterapia en casa para intentar que consiga llegar lo más lejos posible pero necesita tu ayuda para continuar. ¿La ayudas?