Teamer desde: 02/12/2017
¡POR LA RESIDENCIA! Somos una asociación sin ánimo de lucro que trabajamos desde 2002 por y para la plena integración de las personas con discapacidad psíquica de nuestra población y los pueblos a nuestro alrededor. Hoy atendemos a 20 usuarios y a sus familias y tenemos en marcha un Club de Ocio y un Centro Ocupacional con Aula de Día Integrada. Queremos conseguir con el esfuerzo de todos una RESIDENCIA donde nuestros hijos tengan una vida normalizada e integrada en la sociedad. ¡POR ELLOS!
Teamer desde: 04/12/2017
Every day, children with Dravet syndrome experience epileptic seizures that threaten their development and quality of life. We are a foundation created by families who refused to give up. We promote innovative research and connect scientists, healthcare professionals, and industry partners to accelerate the development of effective treatments. With just €1 a month on Teaming, you can help us bring closer a future with fewer symptoms and more opportunities for people living with Dravet syndrome.
Teamer desde: 15/03/2018
We give DRINKING WATER to families in Yemen who were displaced from their homes. Yemen is one of the biggest humanitarian emergency on the planet and is suffering from a cholera epidemic and shocking infant mortality. With your EURO we buy and refill WATER TANKS in IDP camps and schools. We have 57 in 4 camps and in 5 schools. More than 9 000 people receive water (more than 800 thousand litres/month). Yemen needs more water! 1€=101 litres in the north and 129 in the south. JOIN US!
Teamer desde: 09/01/2020
1 euro per month to promote the cure of rare and complex epilepsies through the scientific research network Indre ApoyoDravet: 14 groups and 20 projects. These diseases describe a world of uncontrolled epileptic seizures, severe cognitive and behavioural impairment, and high degrees of disability and dependence. More than 80,000 people are affected, with a mortality rate of around 25% and costs in excess of €20,000. A research effort coordinated by Dr. Aras
Teamer desde: 10/06/2020
Somos un grupo de niños/as que tenemos el síndrome de duplicación mecp2, que nos produce retraso mental, psicomotor y de lenguaje, insomnio, infecciones respiratorias, esteriotipias… crisis epilépticas que nos producen regresión. En el hospital Sant Joan de Deu de Bcn se investiga gracias a las familias y a las donaciones privadas para encontrar un tratamiento o cura que mejore nuestra calidad de vida.Necesitamos tu ayuda! www.duplicacionmecp2.es