Barbara Farras

Aspanias és una associació sense ànim de lucre amb més de 50 anys d'història. Ajudem a persones amb discapacitat intel.lectual i / o diversitat funcional a través de: - pisos tutelats per a adults amb discapacitat intelectual - cdiap per a nens i nenes desde 0 fins a 6 anys amb necessitats de teràpies (logopèdia, fisioterapia, etc) - assessorament a famílies - altres teràpies (gossos, música, etc) Amb només 1 euro al més ens pots ajudar a seguir creixent junts!

La Asociación de Hemiparesia Infantil - HEMIWEB es una plataforma de apoyo mutuo de padres y madres de niños con hemiparesia, hemiplejía y trastornos asociados. Nuestro objetivo es unir a las familias para promover cambios y concienciar a todos los ámbitos sociales de la existencia de la HEMIPARESIA, que sigue siendo poco conocida a pesar de su elevada frecuencia (1/1000), mejorar su prevención, tratamiento, investigación y, en especial, la calidad de vida de los niños y jóvenes con hemiparesia.

La Fundación tiene como misión promover las actividades de la Asociación de Hemiparesia Infantil, apoyar a las familias de niños/as con HEMIPARESIA - HEMIPLEJIA, concienciar a todos los ámbitos sociales de la existencia de la hemiparesia, que sigue siendo poco conocida a pesar de su elevada frecuencia, y mejorar su prevención, tratamiento, investigación y, en especial, la calidad de vida de los niños y niñas y sus familias.

Xènia is a pretty little girl became tetraplegic due the enterovirus outbreak happened in Spain on 2016. She had the most agressive strain, D68 that made several damages in her spinal chord. She's been in the PICU for 3 months having 3 heart attacks and 2 pneumonia, and she recovered succesfully. After that we'd been in Guttmann Institute, a recovery center for 6 months. We're fighting to keep her as healthy as possible Follow us in: https://www.facebook.com/helpxenia/ Thank you so much,

Daniel is five years old, lives in Uganda and in 2019 he had a stroke. Since then he can barely move his left arm and leg. He is on chronic medication, he needs splints, jabs... which the Ugandan healthcare system does not take on, the cost is on the family, which barely manages to subsist. We need your help so that this little one can continue to grow up happily and, like our children, have the right to health care and treatment.

Funded by the renowned pediatric surgeon Dr Raül Abella, was created with the aim of: * Helping, accompanying and supporting children who are born with heart diseases and providing assistance to their families. * Bringing resources to children in need of medical procedures to be operated in Barcelona through international treaties and agreements. * Training medical personnel from other countries who do not have expertise. We treat heart diseases with excellent results.