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Noah Higón during his participation in the first day of the International Congress of Rare Diseases that this year has been held in an 'online' format

My voice will never stop fighting; nothing is impossible

The testimonies of Noah Higón, diagnosed with seven rare diseases, and Sonia Torres, mother of a child affected by one of these pathologies, have opened the 13th International Conference on Rare Diseases, organised by D’GENES and UCAM, an event that until Thursday brings together 900 participants from 20 countries online

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Moment of the meeting in which it was decided to launch the investigation (File photo)

UCAM opens up to crowdfunding a pioneering research to cure multiple sclerosis

The project, included in the Precipita platform of the Spanish Foundation for Science and Technology (FECYT), which belongs to the Ministry of Science and Innovation, is directed by the UCAM researchers Juan Carlos Izpisúa, Professor of Developmental Biology; José Meca, neurologist and Head of Unit at the Hospital Virgen de la Arrixaca and Estrella Núñez, vice-chancellor for Research

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