Divi Reyes

Hi I'm Matthew, I was born giving a scare to my moms on Halloween 2021. I have an ultra-rare disease (BCAP31 gene mutation), 2 cases in Spain and few cases in the world. I have severe bilateral hearing loss, low vision, dystonic spastic tetraparesis, central hypomyelination, epilepsy crisis... Mateo is going slowly but moving forward thanks to the therapies he performs. With your small contributivo, you can help him keep moving forward and hopefully one day he can sit, walk, talk

Somos una ONG que apoya a niños y niñas vulnerables para que crezcan en un entorno seguro y con oportunidades. Implementamos cuatro líneas estratégicas: Protección, Prevención y Desarrollo, Refugiados y Situaciones de Emergencia. Los fondos de Teaming se destinarán a Prevención y Desarrollo. Nos centraremos en la provisión de alimentos nutritivos para combatir la desnutrición, garantizando el bienestar y el crecimiento de los niños que más lo necesitan, porque JUNTOS PODEMOS.

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.

Anita tenía 2 años cuando le diagnosticaron cáncer. Desgraciadamente no pudo superarlo, después de casi 4 años continuos de tratamientos, la falta de investigaciones sobre su tumor y por tanto de tratamientos efectivos para curarla se la llevaron para siempre. Necesitamos abrir investigaciones específicas para los niñ@s, es la única manera de curarlos. Colabora con el Dr. Mora y su equipo en el Hospital San Juan de Dios de Barcelona por solo 1€ al mes. http://www.asociacionanita.org

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 1747 children and their lifes have changed!!. 1 breakfast =€0.59. 1month=€13. TOTAL 3 school/month= €22.711. Your € FEEDS, EDUCATES AND PROTECTS.

Soy Xana, tengo 14 años, y soy maravillosa, pero como todo no puede ser perfecto, tengo Parálisis cerebral, y llevo una traqueotomía para respirar, y una válvula para la hidrocefalia. Pase un año en la UCI, y por todo eso aún no hablo, pero soy muy peleona, así que seguiré luchando! Mis padres han creado este grupo, para poder costear las terapias que necesito que son muchas! Gracias! Podéis visitarme en www.facebook.com/xanapuede.

Can you imagine being afraid to hug your child? This is how the parents of Butterfly Children feel. A rare and incurable condition, which causes the skin to break with the slightest touch. DEBRA-BUTTERFLY CHILDREN CHARITY works to improve their quality of life. By joining this group you are giving them wings.

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. Will you join us?

Did you know that 5,000 people get sick with leukaemia each year in Spain, which is the most common childhood cancer, and that despite the progress made, we still lose one in four minors and half of adults? At the Josep Carreras Foundation we have been working for more than 30 years to make leukaemia a 100% curable disease, to find 100% compatible donors for everyone, and to make displaced patients feel at home. With your help, we are unstoppable.