Ley de Fibrosis Quística: una lucha colectiva

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Tras la aprobación en el Senado de la Ley de Fibrosis Quística, nos comunicamos con Carlos Monteverde, integrante de la Red Argentina de Instituciones de Fibrosis Quistica y padre de Sabrina Monteverde, una joven de 22 años con fibrosis quística que se viralizó tras filmar un video pidiendo para que su obra social le cubra el tratamiento.

Episode metadata supplied by the publisher feed · Published Jul 28, 2020

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Ley de Fibrosis Quística: una lucha colectiva

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