Pablo Almendral Jimena

Soy Martín y nací con una condición genética muy poco frecuente, mutación del gen CASK que afecta mi desarrollo neurológico: tengo dificultades motoras, visuales, del habla y deglución. Por ello asistimos a terapias semanalmente: 2h Rehabilitación, 2h Logopedia, 2,5h T.Ocupacional, 2h Terapia Visual y 3/4 semanas/año intensivos de fisioterapia en Alicante. Cada sesión me ayuda a moverme mejor, comunicarme más y ganar autonomía. ❤️ Gracias por acompañarme en este camino y por creer en mí.

At Teaming, more than 400,000 people Change Lives with €1 a month. For more than 10 years we have been helping all kinds of social causes to get financial help completely free of charge and constantly. Together we have raised more than 60 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?

Help Pablito Move Forward Pablito is a brave 3-year-old with cerebral palsy, epilepsy, low vision, and severe neurological challenges. He needs intensive therapies and a pediatric exoskeleton to improve his quality of life.With €1 a month, you can help change his future. Join our Teaming group and be part of this wave of hope for Pablito. Thank you for your support.

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