Carles Bosch Badia

The SJD Pediatric Center is the first monographic centre for paediatric oncology in Spain (2nd in Europe). 70% of the centre is devoted to care and 30% to research. It has the capacity to care for 400 children and youngsters. Its spaces are designed with the emotional well-being of the children and their families in mind. Our aim is that the children have more options to overcome cancer with less after-effects. Will you join us?

Colaboración para alimentar y cuidados veterinarios de dos colonias de gatos que hace unos años gestiono para que estén lo mejor posible . Gracias por vuestra colaboración. Saludos .

Jorge sufrió una transfusión feto-fetal de su hermano gemelo Cristian a las 36 semanas de embarazo, lo que le produjo una anemia severa. Cristian no tuvo tanta suerte y murió. Tras 17 días en la UCI, parecía que Jorge iba evolucionando bien, pero con el tiempo le diagnosticaron una parálisis cerebral. Desde entonces le hemos estado ayudando con muchas terapias y aparatos ortopédicos. Tenemos un sueño: que pueda andar. ¿Nos ayudas a hacerlo posible con 1€/mes?

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

ASPACE Soria is a non-profit association that aims to comprehensively cover the needs of people with cerebral palsy, related pathologies and other disabilities in the province of Soria. We provide specialised services and treatments. Our attention addresses problems of movement, learning, speech, swallowing, hearing, psycho-social and emotional development. Our aim is that both users and families have the best possible quality of life.

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?

ALS is a neurodegenerative disease of unknown origin, without a cure and with a life expectancy of 2 to 5 years. Affected people are aware of the progressive loss of motor functions and the increasing degree of dependency. The Catalan Foundation for ALS Miquel Valls is the only non-profit organization in Catalonia that works to improve the quality of life of people and families affected by ALS through psychosocial support projects at home and in hospitals.

La Asociación Abay nace desde un profundo sentimiento de amor y respeto por Etiopía. Somos una asociación sin ánimo de lucro formada por personas interesadas en participar el desarrollo del pueblo etíope. Nuestro principales proyectos están en Walmara y Addis Abeba. www.abayetiopia.org

We provide care and guidance to people living on the streets of Barcelona. We guide them towards a more autonomous life, covering their basic needs, providing social care and guaranteeing accommodation for those in the most vulnerable situations. We also work to raise awareness, denounce unjust situations and provide solutions to make #nobodysleepinginthestreet possible. Become a Teamer and collaborate by contributing 1 euro a month!

Join our Teaming and bring smiles to those who need them most. At Pallapupas, we bring humor and joy to hospitals, turning fear and pain into hope. With just €1 a month, you help more children, adults, and elderly patients receive a visit from our clowns. Because laughter is healing, and together, we create magic. Join Pallapupas and change lives with a smile.

CADASIL is a rare hereditary disease that affects arteries throughout the body, but its symptoms only occur in the brain, with recurrent strokes and dementia at an early age (around 45-50 years old) being characteristic. There is NO cure, but a research team at the Hospital de la Santa Creu i Sant Pau (Barcelona) is going to start a clinical trial to see if treatments already on the market can help to stop this incapacitating disease. We need you! Help us to cure!

Somos una Fundación que trabajamos para mejorar la calidad de vida de las personas con discapacidad física o problemas de mobilidad a través del deporte y la actividad física. Queremos conseguir que el máximo de personas pueden acceder al deporte o al ejercicio físico de forma integrada.

Carlos, a NTT DATA partner, was diagnosed with ALS at the age of 32. Since then, he has tirelessly fought against the disease and is now a remarkable example of perseverance: he has covered over 1,000 km in 17 marathons in his wheelchair. Through this Teaming Group, NTT DATA colleagues support the Luzón Foundation's project "Giving a Voice to People with ALS," which provides alternative communication devices to those with fewer resources. With just €1/month, you too can give them voice. Ready to join us?

Somos la familia de Yessica Martínez Romero, una niña de 22 años que desde los siete padece una enfermedad neurodegenerativa que a día de hoy sigue sin diagnóstico. Desde hace más de cinco años está en una silla de ruedas. Hemos viajado por infinidad de hospitales buscando una solución y seguimos necesitando ayuda para lograr un diagnóstico, además de gastos de investigación, cuidados y médicos. Toda la información: https://www.facebook.com/groups/247145705431108/ GRACIAS.

Marta is the first child diagnosed with Opitz C Syndrome (www.asopitzc.org) in Spain. It is a serious and unknown disease that makes Marta be totally dependent. We promote the research carried out by a team from the University of Barcelona. To continue with the project, it is essential to continue raising funds for this research team. The first objective, to locate genetic mutations, is already being achieved. Now, we must go on to find therapies that help these children.

Soy Xana, tengo 14 años, y soy maravillosa, pero como todo no puede ser perfecto, tengo Parálisis cerebral, y llevo una traqueotomía para respirar, y una válvula para la hidrocefalia. Pase un año en la UCI, y por todo eso aún no hablo, pero soy muy peleona, así que seguiré luchando! Mis padres han creado este grupo, para poder costear las terapias que necesito que son muchas! Gracias! Podéis visitarme en www.facebook.com/xanapuede.

SEVIHDA financially supports ASPOV (Association for Life), a non-profit association that provides psychosocial care to children affected by HIV and their families in the region of Piura (Peru), where they have HIV It leads to a stigma and social isolation, especially if you are a woman, because of the false myths about transmission and treatment, which often cause the person to end up with depression, abandonment of treatment and even death.

Hola me llamo Triana ! Padezco el síndrome Gabrielle de vries una mutación de novo genética muy rara , tan rara que solo en España somos 2 casos . Con sólo 1€ al mes mía papás pueden seguir pagando toda mi rehabilitación físico-cognitiva. ¡ GRACIAS POR QUERER AYUDARME !

At Teaming, more than 400,000 people Change Lives with €1 a month. For more than 10 years we have been helping all kinds of social causes to get financial help completely free of charge and constantly. Together we have raised more than 60 million euros and, as long as social causes need us, we will continue to support them. With this Teaming Foundation Group we make it possible. Will you join us?

In response to the impact of the cold drop in Spain, NTT DATA colleagues have launched this Teaming initiative to support individuals and families affected by the floods and their aftermath. Together, we can make a meaningful difference by each contributing a small amount. Through the Red Cross, our support will provide immediate relief, including shelter and essential supplies, as well as longer-term assistance with recovery and rebuilding. Will you join us with just €1 a month?

We are a family from Spain. Our son Mateo, has a genetic mutation in the NEK8 gene, considered ultra rare, that is damaging his organs. When he was 9 months old, he had a liver transplant and when he was 3 years old, a kidney transplant. In a future he could need a heart transplant, also. There is a research team that can help him to stop his illness but they need funding (€62,000). Your contribution can save him.

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!

Claudia, con tan solo 6 años se encuentra afrontando mil batallas, las que le acompañan en esta enfermedad genética y muy rara denominada "MENKE-HENNEKAM", en la que apenas hay diagnosticados 80 casos en todo el mundo. Los problemas que le genera son tanto físicos como neurológicos. Así que lanzamos esta campaña para recaudar fondos y así aportarlos a la investigación de su enfermedad. @lasmilbatallasdeclaudia Mil gracias a todos♥️

Hola mi nombre es Valentina, sufro una enfermedad ultrarara siendo el primer caso en España y en el que se conocen menos de 30 casos en el mundo, Polineuropatia Hipomielinizante Congénita tipo 3 una mutación en el gen CNTNAP1. No hay tratamiento ni cura en la actualidad, un equipo de investigación liderado por José Antonio Sánchez Alcazar de la universidad de Pablo de Olavide, inciará una investigación para la enfermedad de Valentina, en la que necesitamos 50.000€ al año, nos ayudas?