Mila Gerova

Yemen is living a brutal humanitarian emergency. The girls are married off in hopes that they will be fed. The boys are recruited as soldiers. Their lives are hell: rapes, pregnancies, violence. If the school provides food, families are more likely to bring them. We give milk, bread, egg/cheese/tuna and fruit to 1680 children and their lifes have changed!!. 1 breakfast =€0.56. 1month=€13,2. TOTAL 3 school/month= €20.698. Your € FEEDS, EDUCATES AND PROTECTS.

SICAR cat programme provides comprehensive care to women who are victims of human trafficking for their recovery and the restoration of their rights. It also organizes awareness and denounce actions in order to contribute to social change.

Hola, soy Hugo Dato. Un mal diagnóstico pediátrico durante el confinamiento me causó un infarto y una lesión cerebral con tan sólo 15 meses. Ahora lucho por volver a ser el que era. Sin embargo, la seguridad social apenas cubre mis tratamientos de rehabilitación, y por eso mis papás están llevando a cabo esta campaña de recaudación de fondos. ¿Me ayudas?

The SJD Pediatric Center is the first monographic centre for paediatric oncology in Spain (2nd in Europe). 70% of the centre is devoted to care and 30% to research. It has the capacity to care for 400 children and youngsters. Its spaces are designed with the emotional well-being of the children and their families in mind. Our aim is that the children have more options to overcome cancer with less after-effects. Your euro helps to carry out the humanisation programmes and new treatments. Will you join us?

Soy Marco y Tay-Sachs ha marcado mi vida ya que mi hijo Liam la padecía. En España hay, en este momento, 13 niños y niñas afectados por las enfermedades de Tay-Sachs y Sandhoff. ACTAYS recauda fondos para financiar la investigación y gracias a personas como tú hemos logrado que 2 universidades estudien Tay-Sachs y Sandhoff. Te necesitamos por todos los niños que padecen estas enfermedades, presentes y futuros. 12 Teamers= 1,5h de investigación.

GAB is an association that fights against the mistreatment and abandonment of the Ratonero Bodeguero Andaluz. This breed is used for hunting and when they are "no longer useful" they are abandoned. It is the same problem as with galgos and podencos, except that the bodegueros are not such a well known breed. The money raised goes directly to pay for the dogs' homes, which cost 100 euros per month per dog, plus countless veterinary expenses. Every euro counts to keep saving dogs.

Somos una Fundación que trabajamos para mejorar la calidad de vida de las personas con discapacidad física o problemas de mobilidad a través del deporte y la actividad física. Queremos conseguir que el máximo de personas pueden acceder al deporte o al ejercicio físico de forma integrada.

Alba is an inteligent funny and amusing girl. Although we well could say “was”, as a terrible tragic accident happened on fateful march 21st 2016. A relative, who was in a shock due to an epileptic attack, let Alba fall from a third floor. Alba saved her life, but a strong brain damage remains on her. Now, we have a long neurorehabilitation process left ahead to see how much she can recover and become herself again a bit. Help us!

We provide care and guidance to people living on the streets of Barcelona. We guide them towards a more autonomous life, covering their basic needs, providing social care and guaranteeing accommodation for those in the most vulnerable situations. We also work to raise awareness, denounce unjust situations and provide solutions to make #nobodysleepinginthestreet possible. Become a Teamer and collaborate by contributing 1 euro a month!

The Association “Poetic Justice” is a nonprofit organization whose main objective is the judicial an extrajudicial defense of sexual abuse victims. We fight against the corruption that is beneath the system and against all injustices that we can deal with. We dream of changing the world by doing our bit. And we´ll change it! Help us, and we´ll change it!

Jimena es una niña de 2 añitos con una enfermedad rara, llamada síndrome de Angelman. Este síndrome afecta a 1 de cada 20.000 nacimientos. Su pronóstico es muy duro, con dificultad para caminar, ausencia del lenguaje, retraso metal, hiperactividad y epilepsia entre otros trastornos. A día de hoy no existe cura, y en el 95% de los casos la causa es puro azar. Para paliar todo esto se precisan costosas horas de rehabilitación y terapia, además de la adaptación de elementos utilizados a diario.

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.