Zoraida María Megias Sierra

Zoraida María Megias Sierra

Almería, Spain


Teamer in 5 Groups

Contributes every month: €5 to 5 Groups

Since 24-12-2020 has contributed €151

Groups supported

5

€40,503 Raised

435 Teamers

Teamer since:  24/12/2020

LA HUELLA ROJA ALMERIA

Somos un grupo de voluntarios que invertimos nuestro tiempo y dinero en salvar animales de la calle y de la perrera, especialmente los mas necesitados, recuperándolos y buscándoles una familia. No tenemos ningún tipo de financiación económica. Tenemos más de 70 animales que buscan un hogar, muchos de ellos llevan años con nosotros. Solo las facturas veterinarias mensuales alcanzan los 3.000 euros y otros 1000 en alimentación. ¿Nos ayudas a seguir salvando vidas?


€62,852 Raised

919 Teamers

Teamer since:  24/12/2020

Wear your wings for the Butterfly Children

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.


€150,600 Raised

1,669 Teamers

Teamer since:  27/02/2023

Welfare flats - Josep Carreras Leukaemia Foundation

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.


€52,768 Raised

659 Teamers

Teamer since:  27/02/2023

Our fight against brittle bone disease

When Martina was 2 months old, she broke her two legs while into her mothers arms. Since then, she has suffered multiple fractures that prevent her from walking normally. Our daughter suffers from Osteogenesis Imperfecta, better known as brittle bone disease. 100% of the collected funds go to entities and projects committed to improving the quality of life of patients.


€1,101 Raised

59 Teamers

Teamer since:  27/02/2023

SCN8A España

Asociación sin ánimo de lucro con 19 familias en España con niños con una mutación genética, SCN8A, muy poco frecuente. Nuestros niños pueden sufrir una encefalopatía muy severa, con crisis epilépticas de muy difícil control y otros síntomas, como discapacidad motora y/o intelectual, rasgos autistas... Necesitamos fondos y gracias a la ayuda de los Teamers y otras iniciativas, hemos participado ya en la financiación de un proyecto de investigación. Si quieres conocernos visita: ww.scn8a.es