La Fundación Isabel Gemio hace visibles las Enfermedades Raras

6 de octubre de 2015

La presidenta de la Fundación Isabel Gemio en Semana.

Desde el origen de la Fundación en 2008, Isabel Gemio ha dedicado toda su energía a la recaudación de fondos para fomentar la investigación sobre las distrofias musculares y otras enfermedades raras. A pesar de reconocer que no es fácil conseguir dinero, la periodista se muestra optimista y destaca que gracias a la ayuda de todos y a través de la investigación se conseguirá algún día que estas patologías dejen de ser incurables.

Podéis leer el artículo en: Reportaje Isabel Gemio 3947

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