Céline Beaulaton

Miwadagbé significa "Pratica o bem". Miwadagbe è uma associação beninense de pais e amigos para a inclusão dos menores portadores de deficiência intelectual, distúrbios do espectro de autismo e/ou de distúrbios psíquicos. Nosso objetivo è de apoiar as ações desta associação dinâmica que precisa de ajuda para desenvolver suas ações. Juntos tudo è possível !

We give DRINKING WATER to families in Yemen who were displaced from their homes by 10 years of war. Yemen is 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 50 in 4 camps and in 5 schools. More than 000 9people receive water (800 thousand litres/month). Yemen needs more water! 1€=101 litres in the north and 129 in the south. JOIN US!

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.

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.

Soy Marco y Tay-Sachs ha marcado mi vida ya que mi hijo Liam la padecía. En España hay, en este momento, 13 niños y niñas afectados por las enfermedades de Tay-Sachs y Sandhoff. ACTAYS recauda fondos para financiar la investigación y gracias a personas como tú hemos logrado que 2 universidades estudien Tay-Sachs y Sandhoff. Te necesitamos por todos los niños que padecen estas enfermedades, presentes y futuros. 12 Teamers= 1,5h de investigación.

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

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.

En la Asociación Baila con EM nuestro lema es "No esperes a que pase la tormenta, aprende a bailar bajo la lluvia". Sois muchos los que os habéis sumado a esta lucha por la mejora de la calidad de vida de las personas con Esclerosis Múltiple; y ya hemos conseguido más de 142.000€ íntegros para la investigación de esta y otras enfermedades como la ELA y el Cáncer de mama. Te necesitamos para seguir imaginando un mundo mejor. ¡Baila con nosotros donando 1€ al mes!

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!

Following Israel's relentless and indiscriminate attacks on Gaza over several months of war, families are drinking unsafe water and going days without food. The health system has completely collapsed amid outbreaks of disease and serious injuries caused by the constant bombardment. Despite this, our teams continue to work tirelessly to save lives.

Cada día nacen 10 bebés con cardiopatías congénitas en España. En su primer año de vida, 1 de cada 3 necesitará ser ingresado lejos de su casa una media de 26 días. En Menudos Corazones, trabajamos para mejorar la vida de estos niños, niñas y sus familias. Con el programa de alojamiento, damos un Hogar gratis cerca del hospital donde descansar y recobrar fuerzas, de modo que su única preocupación sea su peque. Uniéndote a nuestro grupo, juntos, conseguiremos 1 Hogar por 1€ para estas familias.

More than 500 patients and their families suffer intestinal failure in Spain. This pathology prevents them from feeding and hydrating themselves naturally. Therefore, they depend on a pump that administers the necessary nutrients intravenously and, sometimes, they need a transplant of up to 6 organs to survive. NUPA is the only national association of affected people. With your help, we will cover the needs of admitted families, providing emergency psychosocial support. Collaborate!

Our son Jesus was diagnosed with a new leukodystrophy, a devastating disease that affects quality of life and hope for a full future. We have formed an association called "THE HONEY OF LIFE" with the aim of financing research in Amsterdam that brings us closer to a cure. The key to defeating this disease is research and the generosity of people like you. Each € is a declaration of hope, a vote for life, and a show of solidarity.

Soy Gabriela, el 07/06/21la vida de nuestra familia cambio, fui diagnosticada de una enfermedad ultrarara, neurometabólica,y letal.Caracterizada por cataratas congénitas, pérdida auditiva neurosensorial, retraso grave del desarrollo, hipotonía muscular grave, así como anomalías del sistema nervioso central.No hay cura en la actualidad, y solo 6 casos descritos.En Navidad un post se hizo viral en instagram @princesagabrielita.Y un equipo de investigadores conctacto con mi familia.Nos ayudas??

I'm Martin, they call me Tintin, I'm 3 years old. I was born with some malformations and one of them was a cleft lip, for which they operated on me when I was 3 months old. They had given my parents full assurance that it would be a simple operation, but something went wrong and I ended up in the Ucip with mechanical ventilation and deep sedation, and one day, they accidentally extubate me and I went into cardiorespiratory arrest for 15 min, and because of that accident I have cerebral palsy.

At the Hospital de Sant Andreu in Manresa, we would like to build a new centre where we can support better people in end of life processes and their loved ones. We would like to ask your help and contribution towards the estimated cost of one room to make the aim to support & care the person and their families from the beginning of palliative care to the end of life, as well as the bereavement process. All new rooms and areas are designed to make a home-like feeling possible.

Grandes Amigos es la ONG de voluntariado,que trabaja desde 2003 para ofrecer compañía, afecto y amistad a las personas mayores que sienten soledad no deseada. Buscamos mejorar su calidad de vida y su salud, que puedan envejecer con dignidad y disfrutando plenamente de sus derechos, y que toda la sociedad se enriquezca con su participación. Somos una herramienta de participación ciudadana basada en compartir compañía y amistad vecinal en torno a las personas mayores. www.grandesamigos.org

Founded by famous Dr. Jane Goodall (Messenger of Peace of the UN and Prince of Asturias Award), the IJG is a non-profit organization in the conservation, rescue and rehabilitation of orphan chimpanzees in Africa (visit www.janegoodall.es). Your euro will be transformed into needed food and medicine, and also into local employment and educational activities with the communities of Congo and Senegal. Each month, for the equivalent of a coffee, YOU can make a difference for many living beings...

In South Sudan, the desperation caused by lack of food, violence, and insecurity drives children into extreme hopelessness. 100% of them suffer from hunger, 80% have thought about suicide, and 33% of children under 12 have already attempted it at least once. With just €0.50 a day, we provide them with one meal at school and help them continue their education, giving them a chance for a future. In small gestures, like giving €1, great miracles are born.

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!

We rescue abandoned and mistreated animals all around Spain. With your support, all of us together can make this possible! Just 1 euro a month can help us a lot to make these animals' dreams come true!

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?