Teamer da: 08/08/2018
Asociación GATA,non profit entity whose mission is rescuing hurted left on their own cats out of streets and shelters to definitely find them an appropriate safe home. Find out more at www.asociaciongata.com and www.gataweb.com All the raised funds are entirely used to cover medical assistance and other daily costs all along the adoption process. Contact us at Info@gataweb.com
Teamer da: 08/08/2018
Fondazione per la ricerca scientifica e l'educazione speciale per i bambini affetti da malattie rare, disturbi generali del linguaggio e capacità di apprendimento.
Teamer da: 08/08/2018
Riesci a immaginare di aver paura di abbracciare tuo figlio? Ecco come si sentono i genitori delle persone con la pelle di farfalla. Una malattia incurabile e sconosciuta che causa la caduta della pelle al minimo tocco. DEBRA-PIEL DE MARIPOSA è un'associazione senza scopo di lucro che lavora per migliorare la qualità della vita. Unendoti a questo gruppo, stai dando loro le ali.
Teamer da: 08/08/2018
Somos una asociación sin ánimo lucro con la finalidad de mejorar la calidad de vida de las personas con discapacidad intelectual. Para lograrlo, hemos fundado un centro de empleo en Madrid en el que ya disfrutan cinco personas de un contrato indefinido. Mantener el centro abierto está siendo muy difícil y corremos riesgo de cierre por motivos económicos, ¿nos ayudas a seguir? Mas info: https://www.facebook.com/LaSonrisaDeGuille/ www.LaSonrisaDeGuille.ORG
Teamer da: 08/08/2018
Somos una Institución privada y sin ánimo de lucro. Tenemos un centro de Acogida y Adopción de perros y gatos abandonados, gestionado por voluntarios y cuyo objetivo principal es encontrarles un verdadero hogar. We are a private non-profit organization that runs a rescue and adoption centre for abandoned dogs and cats with the help of volunteers. Our aim is to find them a real. Necesitamos recaudar fondos para la alimentación, los gastos veterinarios y el bienestar de nuestros animales.
Teamer da: 05/10/2025
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
Teamer da: 05/10/2025
On May 2, 2022, you arrived through the big door at only 25 weeks gestation and weighing 470gr/1,03lb.Your unwavering strength allowed you to overcome challenges throughout 8 months in the UCIs Where you taught us powerful lessons about courage and extreme love, a love that constantly tries to protect you even from the death that so many times knocked at the door. The battle continues, we need help with your therapies and vital resources for your development . Will you help us not to fail Roi?
Teamer da: 05/10/2025
Somos un grupo de mujeres que estamos pasando por diferentes etapas de cáncer de mamá con un tumor clasificado como triple negativo y que tenemos un proyecto en común: Formar esta asociación para ayudar a recaudar fondos para proyectos de investigación específicos para el triple negativo y ayudar a la divulgación de este tumor con información actualizada.
Teamer da: 05/10/2025
Hola soy José Codina, presidente de la Asociación Recuérdame el principio de la desconexión, constituida el 16 de diciembre de 2020 en inscrita en el registro nacional de Asociaciones el 23 de abril de 2021. Actualmente unas 800.000 personas padecen Alzheimer en nuestro país según datos de la Sociedad de Neurología. Cada año se diagnostican 40.000 nuevos casos. ¿Porque pedimos que nos ayudéis? Porque no tenemos ninguna subvención ni ayuda de las administraciones publicas.
Teamer da: 05/10/2025
Help us raise funds that will be donated to research and treatment of the rare degenerative genetic disease called facioscapulohumeral muscular dystrophy (FSHD), which is characterised by marked facial inexpressiveness and progressive muscle weakness. Those affected experience varying degrees of disability, eventually losing the ability to walk and becoming totally dependent on others for much of their lives. ww.fshd-spain.org