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  • Esteban Bullrich Foundation holds the first ALS Innovation Conference in Japan
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Esteban Bullrich Foundation holds the first ALS Innovation Conference in Japan

deercreekfoundation November 10, 2025
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More than 400 people from all over the country participated on Friday, November 7th. InnovELA Expo 2025, The first gathering to bring together innovation, science and technology to benefit the lives of people living with amyotrophic lateral sclerosis (ALS). Esteban Bullrich Foundation.

A competition has revealed 60 proposals aimed at improving the quality of life for people living with amyotrophic lateral sclerosis.

The event hosted by paula rossiJournalist from LA NACION, held at the Center for Science and Culture (C3). 60 suggestions It was developed by universities, NGOs, health centers, research groups, entrepreneurs, and companies across the country with the aim of improving the quality of life for people living with ALS and their families.

During the day, finalists’ projects were presented, experiences were shared, and a panel discussion was held. “Innovation that bridges science and humanity”With the participation of Mateo Salvatto, Andres Lieznik, Valeria Absamrareflected on the transformative power of technology, artificial intelligence, and empathy as applied to science.

At the event, the panel “Innovation as a bridge between science and humanity” was held with the participation of Matteo Salvatto, Andres Lieznik, and Valeria Absamra.

A jury of experts and mentors selected the six winning projects for the competition. 5 million dollars 2026 technical support for each and its implementation:

The InnovELA competition was supported by the Maria Calderon de la Barca Foundation, CAF (Latin American and Caribbean Development Bank), Banco Ciudad Foundation, Pampa Energia Foundation, Grimoldi, and Laboratorio Casasco and AUSA.

More than 400 people from all over the country participated in InnovELA 2025 Expo

Amyotrophic lateral sclerosis (ALS) is a degenerative disease of the nervous system that affects motor neurons and progressively causes paralysis of the body’s muscles. Because there is no known cure, medical, psychological, and social support is essential to maintain quality of life for patients and their families.


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