At the Foundation, we focus on four areas to provide support to the entire ALS community:
We are committed to providing assistance, counseling, and creating spaces for patients and their families to interact.
RegisterWe facilitate the participation of Argentine patients in research on treatments developed in other countries and promote local research.
See projects
We are dedicated to training healthcare professionals and students
to achieve early diagnosis of ALS and to provide proper care for
patients and their families.
Our goal is to enhance the knowledge and skills required to
address this disease comprehensively so that we can offer more
effective support to those in need.
Our goal is to increase awareness and share information about ALS
through media campaigns and social networks, as well as to
participate in and host events.
We aim to provide important information in a manner accessible to
patients, family members, and friends and to actively involve the
community in understanding and supporting those with ALS.
Registry of people with ALS in Argentina
RegistrELA is our registration platform for people with Amyotrophic Lateral Sclerosis in Argentina.