Ángel Álvarez Rodríguez

Phelan-McDermid Syndrome is a genetic condition considered a rare disease. Those affected suffer a developmental delay in multiple areas, especially in the ability to speak. Our mission is to improve the quality of life of people affected by the Syndrome through research, support to families and awareness. For more information you can consult our website www.22q13.org.es Visit us on our social networks! @sindromephelan

We manufacture prostheses for people who are amputees or who have been born without an arm. We have delivered hundreds of them in Spain. Mexico, Colombia, Kenya, Thailand and more than 50 other countries free of charge for people with disabilities who could never access this type of aid. Giving them this oportunity would improve their quality of life, increase their employability and, in the case of children in many countries, would allow them to go to school. HELPING IS TOO EASY NOT TO DO IT.

Alba is an inteligent funny and amusing girl. Although we well could say “was”, as a terrible tragic accident happened on fateful march 21st 2016. A relative, who was in a shock due to an epileptic attack, let Alba fall from a third floor. Alba saved her life, but a strong brain damage remains on her. Now, we have a long neurorehabilitation process left ahead to see how much she can recover and become herself again a bit. Help us!

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.

Na Teaming, mais de 430 000 pessoas transformam vidas com 1 € por mês. Há mais de 13 anos apoiamos todo o tipo de causas sociais, oferecendo ajuda financeira de forma totalmente gratuita e contínua. Juntos já angariámos mais de 70 milhões de euros e, enquanto as causas sociais precisarem de nós, continuaremos ao seu lado. Com este Grupo da Fundação Teaming, tudo isto é possível. Quer juntar-se a nós?

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?

A CADASIL é uma doença hereditária rara que provoca a oclusão das pequenas artérias cerebrais, com acidentes vasculares cerebrais recorrentes e demência numa idade precoce (por volta dos 50 anos). Não existe cura, mas uma equipa de investigação do Hospital de la Santa Creu i Sant Pau (Barcelona) vai iniciar um ensaio clínico para ver se os tratamentos já existentes no mercado podem ajudar a retardar esta doença incapacitante. Precisamos de si! Ajude-nos a curar!