Encarnacion Durio Siloniz

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 are a non-profit association consisting only of 28 people affected by Nemaline Myopathy and their families, distributed throughout Spain. MN is a rare neuromuscular genetic disease (1:50,000 births) without a cure and treatment, with almost non-existent study. We have managed to launch a research project. Would you help us improve the future of our beloved ones? We'll be greatly grateful! www.yonemalinica.es

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.

Mala Pata is a project that arises from the need to give more visibility and find families to the races listed as PPP's being these the most discriminated races and with less possibilities of adoption not only because of the ignorance of an audience that does not know them, but for a law that harms them even more. We focus on the kennels of the province of Cádiz and work primarily in its dissemination to give them the opportunity they never had.

We are a group of people affected by multiple sclerosis, a neurodegenerative disease experienced by some 50,000 people in Spain. Two-thirds of the 1,800 people who each year learn they have MS are under the age of 40; three out of four of them are women. GAEM promotes research into treatments for this disease, and seeks to improve the quality of life of affected people and their families. We finance ourselves from the resources of conscious and generous people like you. Will you help us?

Hola mi nombre es Valentina, sufro una enfermedad ultrarara siendo el primer caso en España y en el que se conocen menos de 30 casos en el mundo, Polineuropatia Hipomielinizante Congénita tipo 3 una mutación en el gen CNTNAP1 No hay tratamiento ni cura en la actualidad, un equipo de investigación liderado por Jose Antonio Sanchez Alcazar de la universidad de Pablo de Olavide, inciara una investigación para la enfermedad de Valentina, en la que necesitamos 50.000€ al año, nos ayudas?

Babies Uganda es una ONG que pone todo su esfuerzo e ilusión en salvar de la miseria a niños huérfanos en Uganda. Actualmente ayudamos a mas de 100 niños en los distintos orfanatos con los que colaboramos, la mayoría de ellos menores de 10 años. Reciben comida, casa, educación, sanidad, pero sobre todo, un HOGAR. Babies Uganda es una familia donde los niños se sienten queridos y seguros. EL 100% DE LOS DONATIVOS SE DESTINAN INTEGRAMENTE A ELLOS. MUCHAS GRACIAS POR AYUDARNOS