Lita Prats Rosello

After closing due to the pandemic, we have reopened to generate leisure spaces for people with intellectual disabilities. With the essence of always and fun as the main axis, we want to continue raising awareness and normalizing so that all people feel more integrated, enhancing citizen participation. Without forgetting the families, who need spaces for rest and support while their children are well treated and cared for. Yes, Ludàlia puts the person at the center.

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?

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!

We contribute to fund the mission of the Richi Childhood Cancer Foundation so that all children and adolescents with cancer have a better prognosis and quality of life. More information: http://www.richifoundation.org

Abril is a 8-year-old girl diagnosed with SPG52, with only 55 diagnoses in the world. SPG52 is an ultra-rare disease that causes very serious symptoms such as severe intellectual disability, epileptic seizures and very rapid muscle degradation in the lower body. Abril started walking when she was 3 years old and now at 8 she can hardly move anymore.

Somos un equipo de jóvenes psicólogos que luchamos por mostrar y extender los beneficios de la música en el ALZHEIMER, ya que la memoria musical y las emociones son de las últimas capacidades en perderse. Necesitamos vuestra ayuda. Nuestra misión: concienciar, sensibilizar, formar y expandir la MÚSICA como herramienta y el AMOR como camino, para el manejo de los trastornos del comportamiento (agitación, agresividad...) que acompañan a la enfermedad. El Alzheimer no puede con la música y el Amor.

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

La enfermedad grave de un niño o joven supone un gran impacto para él y para todo su entorno. Por eso, la Fundación Villavecchia acompaña a familias de niños y jóvenes con cáncer u otras enfermedades graves que les limitan la vida. Desde hace más de 30 años la Fundación Villavecchia trabaja para ofrecerles una atención integral y mejorar su calidad de vida en todo el proceso. En estos difíciles momentos, necesitamos tu apoyo para estar más cerca que nunca de estas familias, ¿contamos contigo?

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.

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.

El proyecto tiene como objetivo disminuir la mortalidad materno-infantil. Que no mueran más madres durante el embarazo y el parto por causas evitables. Para ser madre y poder vivirlo! Sensibilizar a la comunidad de la importancia de acudir a los controles prenatales y dar a luz en un centro sanitarios Formación de comadronas, dotación a los centros sanitarios rurales y hospital rural de Gambo del material necesario para atender un parto y sus complicaciones. Y transporte médico

Al Sur de Etiopía, en una región rural y con muy pocos recursos económicos, se encuentra el Hospital de Gambo, hospital misionero que ofrece asistencia sanitaria a todos los habitantes de la región e incluso recibe a las personas más pobres de zonas alejadas al tratarse de uno de los hospitales más baratos del país. La población padece desnutrición severa, deshidratación, malaria, tuberculosis, sida, neumonía, meningitis, y son los niños la población más vulnerable y afectada.

Ainara nació el 21 de noviembre de 2015, a las 10:03h. Pesó 1,030kg. Estuvo a punto de morir 2 veces y tuvo que pasar sus primeros 5 meses de vida en el hospital. Ainara tiene atrofia cerebral, epilepsia, hipotiroidismo, hipotonia (falta de tono muscular), su cuerpo no fabrica cortisol ni hormona del crecimiento y padece un retraso psicomotor severo. Ainara realiza fisioterapia en casa para intentar que consiga llegar lo más lejos posible pero necesita tu ayuda para continuar. ¿La ayudas?

Open Arms opens its arms to women, men, boys, girls and all those fleeing horror, looking for a chance. The humanitarian emergency in the Mediterranean does not stop and our mission is to protect the lives of the most vulnerable at sea, and on land continues. Working in schools on human rights and empathy and denouncing all injustices is our mission as well. From your hand we can prevent more deaths. We need each other. You are needed.

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?

Yemen is living a brutal humanitarian emergency. The girls are married off in hopes that they will be fed. The boys are recruited as soldiers. Their lives are hell: rapes, pregnancies, violence. If the school provides food, families are more likely to bring them. We give milk, bread, egg/cheese/tuna and fruit to 1747 children and their lifes have changed!!. 1 breakfast =€0.59. 1month=€13. TOTAL 3 school/month= €22.711. Your € FEEDS, EDUCATES AND PROTECTS.

Firefighters Help is an Association of Firefighters of Madrid that, seeing the serious situation that society is going through, seeks to help people and/or entities or associations in need with the strength of the group of firefighters. We are helping families in difficulty with shopping baskets, financing therapies for children with severe illnesses and collaborating in research in several hospitals. www.bomberosayudan.org

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?

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!