Mirian Bayo

A cure for our children now exists based on gene therapy (FRF-001). It was developed in a laboratory in the United States, privately funded by parents and investors from around the world. This gene therapy will enable our children affected by FOXG1 syndrome to improve their quality of life, correct their brain malformations, and begin to reach developmental milestones like other children: walking, talking, etc. Will you help us raise funds?

In Teaming, più di 430.000 persone cambiano vite con 1 € al mese. Da oltre 13 anni sosteniamo ogni tipo di causa sociale, offrendo aiuto economico in modo totalmente gratuito e costante. Insieme abbiamo raccolto più di 70 milioni di euro e, finché le cause sociali avranno bisogno di noi, continueremo a restare al loro fianco. Con questo gruppo della Fondazione Teaming tutto questo è possibile. Vuoi unirti a noi?

Siamo un team di psicologi il cui obiettivo è dimostrare e propagare i benefici che la musica ha sul morbo di Alzheimer, dato che la memoria musicale e le emozioni sono le ultime capacità a perdersi. La nostra missione: coinvolgere, sensibilizzare, comporre e diffondere la MUSICA come strumento e l’AMORE come cammino per la gestione dei disturbi comportamentali (agitazione, aggressione...) che accompagnano la malattia. L'Alzheimer non può vincere con la musica e l'amore.

Junior tiene una enfermedad genética llamada Síndrome FoxG1. Entre sus síntomas tiene microcefalia, epilepsia, retraso motor severo, discapacidad intelectual... Junior acude a un colegio de educación especial y además necesita terapias para seguir evolucionando. Actualmente existe una cura a este síndrome basada en terapia génica y los primeros ensayos clínicos llegarán muy pronto. Por eso queremos recaudar dinero y conseguir una cura para Junior. ¿Nos ayudas?

Iria is a small girl diagnosed with Foxg1 Syndrome. This rare disease is a mutation in the Foxg1 gene that affects brain development in its earliest stage causing irreparable damage. Iria has a brain injury called Pachygyria along with dyskinetic cerebral palsy and epilepsy. Our little girl needs therapies to advance her development, so we collect funds. Can you help us ??? We keep walking! For more information: www.elsenderodeiria.com

Hi I'm Matthew, I was born giving a scare to my moms on Halloween 2021. I have an ultra-rare disease (BCAP31 gene mutation), 2 cases in Spain and few cases in the world. I have severe bilateral hearing loss, low vision, dystonic spastic tetraparesis, central hypomyelination, epilepsy crisis... Mateo is going slowly but moving forward thanks to the therapies he performs. With your small contributivo, you can help him keep moving forward and hopefully one day he can sit, walk, talk

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.