“Tonight’s promise is a commitment. Aisla is Concretely, this disease is present in families, in hospitals, in Nemo centers, in research. Tonight the promise is to continue with greater power and greater responsibility and also with love to protect people with disabilities, provide support and assistance where necessary, provide increasingly simple paths for families and above all greater dialogue within institutions so that no one can be left alone.” That’s Fulvia Massimelli, national president of the Italian Amyotrophic Lateral Sclerosis Associationspoke at the event ‘2025 Promise’live marathon bringing together music, entertainment and life stories to support research on amyotrophic lateral sclerosis (ALS), at headquarters
Adnkronos Agency on Piazza Mastai in Rome.
“The Aisla community is a special community, consisting of people who are very fragile but very brave. This community is aware that currently there is still no medicine that can cure this disease, but they have to live and try to live as best they can.
