Marta González Durio

Alba è una bimba intelligente, divertente, carina. Anche se potremmo dire "era", dal fatidico 21 marzo, quando si è verificato un terribile e tragico incidente. Un parente, in uno stato di shock da un attacco epilettico, lasciò cadere Alba dal terzo piano. Alba è stata salvata ma ha subito diversi danni cerebrali. Ora ha un lungo processo di neuroriabilitazione per cercare di recuperare e tornare ad essere un po' quello che era. Aiutala!

Asociación protectora de animales, en Lucena, Cordoba, trabajamos por y para ellos, únete a nuestro grupo para poder seguir haciendolo

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

After 12 years of crisis, humanitarian needs in Syria have reached unprecedented levels. Millions of Syrians have been forcibly displaced to neighboring countries, and the more than 6 million internally displaced are struggling to overcome immense challenges exacerbated by the earthquake of 2023. UNHCR continues to support them with, among other things, stoves and fuel for generating heat, thermal insulation for tents and winter clothing.  Photo © UNHCR/Claire Thomas

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?

Ciao cari Teamers! Qualcuno di voi ci conosce già e confida in noi ogni giorno, lottando insieme per continuare il nostro progetto di aiuto ai più bisognosi. Per chi non ci conosce: Benvenuti nella nostra Pulgofamiglia! Soccorriamo i cani abbandonati o vittime di maltrattamento. Sebbene siamo una piccola e umile associazione, ci occupiamo di tutta Spagna, ma siamo a San Roque, Cadiz. Abbiamo bisogno di voi più che mai per curare i nostri cani e continuare con il progetto.

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

*¿Quiénes somos?* Somos un grupo de personas que sin ánimo de lucro gestionamos colonias felinas en Chiclana De La Frontera desde hace más de 4 años. *¿Cuál es el objetivo de nuestra lucha?* Sencillo, proporcionar ayuda a esos animales que son ignorados por la mayoría de nuestra sociedad. Hemos rescatado y dado en adopción a decenas de gatos, con el fin de dar a un animal inocente una vida digna. *¿De dónde salen nuestros fondos?* A través de Facebook organizamos muchísimas campañas.