Carlota Díaz Caneja Llamas

Guzmán is a boy with a rare disease: Hyper-IgM syndrome, an immunodeficiency that weakens his immune system. On 25/09/2024 he received a bone marrow transplant in Barcelona. With this teaming we help to cover transfers and stays for medical follow-up and support research into rare diseases, especially Hyper-IgM syndrome. Your euro adds up!

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.

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??

Ajudamos mais de milhares de causas sociais a tornar os seus projetos possíveis todos os dias. Desde que lançámos o Teaming, já angariámos mais de 60 milhões de euros para as causas, totalmente livres de comissões. Criámos este Grupo Teaming para ajudar a Fundação Teaming a continuar a ajudar os outros com esta plataforma. Entre outros apoios, graças aos Teamers deste Grupo,o Teaming é totalmente gratuito. O nosso sonho: sermos autossustentáveis graças a este Grupo.