Rome, November 20 – (Adnkronos) – “Tonight’s promise is a commitment. Aisla is real, she is present in the family, in the hospital, in the Nemo centers, in research. Tonight the promise is to continue with greater strength and greater responsibility and also with love to protect people with disabilities, providing support and assistance where necessary, providing increasingly simple paths for families and above all a wider dialogue within institutions so that no one can be left alone”. That’s how Fulvia Massimelli, national president of the Italian Amyotrophic Lateral Sclerosis Association, spoke at the event ‘La Promise 2025’, a live marathon where music, entertainment and life stories intertwine to support research on Amyotrophic Lateral Sclerosis (ALS), at the Adnkronos agency headquarters in 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.
