Pilar Giraldo

Desde hace más de 30 años trabajamos para mejorar la vida de las personas con enfermedades lisosomales y hematológicas raras y la de sus familias. Investigamos para avanzar en su diagnóstico y tratamiento, promovemos el asesoramiento genético y formamos a profesionales. En las enfermedades raras, cada paciente importa y cada avance cuenta. Tu ayuda nos permite seguir investigando, acompañando y buscando respuestas.

Lysosomal Acid Lipase Deficiency (LAL-D) is a rare, serious, and incurable disease. At LAL-D PO, we fight every day to change this. Our goals: - Early diagnosis - Access to proper care - Scientific research to reach our biggest dream: a cure With just €1/month, you can help us move forward. Join our Teaming group and be part of the change. Together we can make it!

At Teaming, more than 430,000 people Change Lives with €1 a month. For more than 13 years we have been helping all kinds of social causes to get constant financial help completely free of charge. Together we have raised more than 70 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?