Your help is important to continue researching |
ALS
40.500+
Approximately People with ALS in America
Jennie Illas Rincon
President of the Association
Danny Salinas
Coordinator of the Association
Committed to helping understand
mitigate the impact
of the disease.
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If you have recently been diagnosed with the disease, you are a family member or caregiver, learn more about the disease, we can help you!
Have you been recently Diagnosed?
We know how difficult it is to receive an ALS diagnosis. Do not hesitate to request information.
Services for the ALS community
Educate yourself and implement strategies to improve the quality of life of people with this disease.
Online Education in ELA
We develop non-formal, virtual education programs aimed at people with ALS, family members and caregivers, organizing courses and conferences to strengthen the technical and emotional capabilities of patients and caregivers.
Partnerships and Cooperation
We establish agreements with national and international organizations, generating joint projects with foundations or related associations, to maximize resources and capabilities in order to meet our objectives.
Research and Development
We promote cross-referenced and peer-reviewed bibliographic research in the different areas involved in ALS, such as nutrition, physiotherapy, respiratory care, psycho-emotional care, and electrostimulation for comprehensive patient management.