En esta serie mensual entrevistamos a pacientes, familiares, científicos, investigadores y líderes hispanos en el mundo de las enfermedades raras, para que nos compartan sus historias, alegrías, desafíos y aprendizajes. Acompáñanos a compartir estas historias, desde la odisea del diagnóstico (¡hablando un idioma diferente!) a los conceptos erróneos en nuestra comunidad. Hablaremos de la diversidad... more
Publishes | Monthly | Episodes | 12 | Founded | 8 months ago |
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Language | Spanish | Number of Listeners | Categories | Health & FitnessMedicine |
Hoy tenemos el gusto de compartir con el premiado cineasta Ernesto Quintero. Nacido en Los Ángeles, California, hijo de padres mexicanos, quienes lo formaron a él y a sus hermanos en un entorno familiar cristiano, inculcando la importancia de la unió... more
Alfredo Gonzalez-Sulser es jefe del laboratorio de investigación preclínica en la Universidad de Edimburgo en Escocia. Su grupo se dedica a investigar la epilepsia y enfermedades del neurodesarrollo en modelos animales. La especialidad del laboratori... more
Analy Navarro, originaria de Guatemala, es la creadora de la fundación BA Hero y autora de cuentos infantiles. Además, ha sido donante de hígado en vida para su hija Julia, a quien le dio una segunda oportunidad de vida. En una entrevista conmovedora... more
Gio (Venezolano), y Kate (Ucraniana), son una pareja que actualmente reside en Canadá. more
Andrés Jiménez Gómez es el director médico del programa de discapacidades del neurodesarrollo del hospital de niños Joe Dimaggio en Hollywood, Florida. Originalmente de Colombia, Andrés ha trabajado en el área de neurología infantil y pediatría en Oh... more
Ana Mingorance es original de Tenerife, España, pero su trabajo la ha llevado al mundo entero en búsqueda de tratamientos para enfermedades raras. Ana, quien recibió su doctorado en neurociencia de la Universidad de Barcelona, nos comparte su experie... more
En este episodio tenemos el placer de compartir las experiencias de Julieta Bonvin Sallago. Esta Argentina radicada en los Estados Unidos hoy trabaja en el hospital Connecticut Children’s. Además, es paciente de Glucogénesis tipo 1A, una enfermedad r... more
En este episodio tenemos el placer de conversar en vivo con Carlos Martinez Villela. Carlos es original de México y su trabajo y pasión es ser defensor de pacientes con enfermedades raras. Tiene experiencia en proyectos de investigación clínica y tra... more
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Gracias Debbie y Vicky por su trabajo para compartir estas importantes historias. Este podcast es un regalo para la comunidad hispana.
Gracias por darnos este podcast con información tan importante.
Apple Podcasts | #189 | Argentina/Health & Fitness/Medicine |
Listeners, engagement and demographics and more for this podcast.
Listeners per Episode | Gender Skew | Engagement Score | |||
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Primary Location | Social Media Reach |
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Mas Que Raras launched 8 months ago and published 12 episodes to date. You can find more information about this podcast including rankings, audience demographics and engagement in our podcast database.
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