Javier Millán González

This Group was created by NTT DATA employees, who have decided to collaborate with the Intheos Foundation. This entity works for finding effective therapies against cancer, based on the development of R+D+i. Intheos Foundation also works on creating awareness with the goal of providing comprehensive care to patients and their families. www.intheos.org

Wir tragen zur Finanzierung der Mission der "Richi Childhood Cancer Foundation" bei, damit alle krebskranken Kinder und Jugendlichen eine bessere Prognose und Lebensqualität haben können. Weitere Informationen: http://www.richifoundation.org

El objetivo principal del proyecto de investigación es evaluar la efectividad de la administración de células mesenquimales en niños con daño cerebral. Se realizará en el Hospital del Niño Jesús de Madrid, pero los niños serán de cualquier lugar de España. Se evaluará la efectividad a nivel motor, a nivel cognitivo conductual, en la reducción de las crisis epilépticas y en la mejoría de la calidad de vida.

Lucia suffers from a terribly painful rare disease, Reflex Sympathetic Dystrophy, with torsional dystonia and myoclonus (convulsive movement disorders). She has been in tremendous pain day and night for almost 10 years. The treatments that she has undergone so far have been unsuccessful, she is getting worse and worse and the disease continues to advance through her body, but we cannot give up, right now we are hoping for something new. We need your help to achieve it.

Fathers and mothers from all over Spain, aware of the seriousness of our children, we decided to fight to give them a better and hopeful future. That is why we have joined together in order to raise funds through the Duchenne Parent Project for research. Currently we have launched 22 research projects in our country aimed at finding a cure or improvement for this disease. Help us to follow, JOIN OUR CHALLENGE! desafioduchenne.org

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.

El objetivo del proyecto es reducir la tasa de abandono escolar de los alumnos con mayores dificultades de aprendizaje, provenientes de entornos socio familiares conflictivos. Además, tiene otros objetivos transversales: eliminación de la brecha de género en entornos tecnológicos, descubrimiento de vocaciones en áreas STEM, soft skills, habilidades sociales y comunicativas, uso del error como parte del proceso de aprendizaje y convertir a los jóvenes en usuarios responsables de tecnología.

At NTT DATA, we want to show our support to our Ukrainian colleagues and all the people suffering the consequences of the war in Ukraine. More than 7 Ukrainian moved inside the country. 8 million have crossed the border. They all have become refugees, mainly women and children. Our help means food, water, blankets, tarps, cash, and legal and psychological support for them. After a year, aid is still needed for them. Join us for 1€/month!

Sin investigación no hay cura. Actualmente no existen tratamientos curativos para las mastocitosis y necesitamos tu colaboración para seguir investigando. ¿Nos ayudas? La piel es el órgano que con mayor frecuencia está afectado, pero también pueden estar implicados la médula ósea, huesos, hígado, bazo, tubo digestivo. Nuestros niños y adultos sufren muchos picores, ampollas, dolores de cabeza y abdominales, diarreas, mareos, malestar general, enrojecimiento facial, osteoporosis, anafilaxias.

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?