Keta Perez
Barcelona, Espanha
Teamer de 10 Grupos
Contribui mensalmente: 10 € para 10 Grupos/projetos sociais
Desde 02-10-2019 contribuiu 246 €
Grupos de que participa
1 468 € Arrecadados
13 Teamers
651 362 € Arrecadados
24 000 Teamers
Teamer desde: 14/07/2022
Ajudamos mais de milhares de causas sociais a tornar os seus projetos possíveis todos os dias. Desde que lançámos o Teaming, já angariámos mais de 60 milhões de euros para as causas, totalmente livres de comissões. Criámos este Grupo Teaming para ajudar a Fundação Teaming a continuar a ajudar os outros com esta plataforma. Entre outros apoios, graças aos Teamers deste Grupo,o Teaming é totalmente gratuito. O nosso sonho: sermos autossustentáveis graças a este Grupo.
56 173 € Arrecadados
1 581 Teamers
Teamer desde: 08/02/2023
Following Israel's relentless and indiscriminate attacks on Gaza over several months of war, families are drinking unsafe water and going days without food. The health system has completely collapsed amid outbreaks of disease and serious injuries caused by the constant bombardment. Despite this, our teams continue to work tirelessly to save lives.
52 231 € Arrecadados
818 Teamers
Teamer desde: 08/02/2023
Syria is at a crucial turning point in its recent history after the fall of the Al-Assad regime, with many challenges still ahead. 14 years of conflict have left 7 mill. people internally displaced and 16 mill. in need of humanitarian assistance. With increasing movements of Syrian refugee families returning to the country with minimal resources, a critical socio-economic situation and a winter that further complicates the situation, immediate assistance is urgently needed to protect them.
47 922 € Arrecadados
312 Teamers
Teamer desde: 08/02/2023
Nearly 12 years of war in Syria have left a country devastated, and worse, millions of lives destroyed. But now a devastating earthquake of magnitude 7.6 hits the northwest of the country and the southeast of Turkey on February 6, leaving more than 4,000 lives in both countries. From the Islamic Relief Foundation we are on the ground providing cash grants so that those most affected can meet their immediate needs.
22 801 € Arrecadados
253 Teamers
Teamer desde: 20/07/2023
More than 500 patients and their families suffer intestinal failure in Spain. This pathology prevents them from feeding and hydrating themselves naturally. Therefore, they depend on a pump that administers the necessary nutrients intravenously and, sometimes, they need a transplant of up to 6 organs to survive. NUPA is the only national association of affected people. With your help, we will cover the needs of admitted families, providing emergency psychosocial support. Collaborate!
26 838 € Arrecadados
355 Teamers
Teamer desde: 20/06/2024
The Dravet Syndrome Foundation transforms lives affected by this rare and severe childhood disease described in 1978. Dravet syndrome, a severe myoclonic epilepsy with mutations in the SCN1A gene, causes frequent seizures, developmental delays, orthopedic problems, speech difficulties, autism spectrum disorders, and growth and nutrition issues. We offer emotional support, research, and awareness efforts to bring hope. Join us and be the change!
76 939 € Arrecadados
1 011 Teamers
Teamer desde: 20/06/2024
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.
16 421 € Arrecadados
846 Teamers
Teamer desde: 08/03/2025
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.
96 € Arrecadados
95 Teamers
Teamer desde: 12/06/2025
En España, 3 millones de personas tienen una de las más de 7.000 enfermedades raras que existen. El 50% de los niños y niñas con una enfermedad rara no tienen un diagnóstico y, para el 94% de estas enfermedades, no existe un tratamiento específico. Las familias tardan una media de 6 años en lograr un diagnóstico y, muchas veces, cuando por fin lo consiguen, es tarde para acceder a una terapia o, tristemente, descubren que no hay ninguna alternativa de tratamiento ni investigación en marcha.