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AEA LAW

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Sanchez has announced $500 million to ensure care for patients with AEA and strengthen the dependency system

It is also planned to create Grade III+ with 24-hour care for patients with ALS and other complex diseases.
(Foto de ARCHIVO)

Celebración tras la aprobación de la Ley ELA durante una sesión plenaria, en el Congreso de los Diputados, a 10 de octubre de 2024, en Madrid (España). El Pleno del Congreso debate y vota el dictamen aprobado por la Comisión de Derechos Sociales y Consumo y las enmiendas mantenidas por los grupos respecto a la Proposición de Ley para mejorar la calidad de vida de personas con ELA y otras enfermedades o procesos neurológicos de alta complejidad y curso irreversible.



Matias Chiofalo / Europa Press

10 OCTUBRE 2024;ELA;ESCLEROSIS;LEY;APROBADA;CONGRESO

10/10/2024

Stock photo: Europa Press.

On Tuesday, the Council of Ministers will approve an allocation of EUR 500 million for the care of patients with Amyotrophic Lateral Sclerosis (AEA)  and the strengthening of the dependency system, as announced by the President of the Spanish Government, Pedro Sánchez, in a post on the X social network.

It isalso planned to create Grade III+ with 24-hour care for patients with AEA and other complex diseases, the refinement of which comes one year after the entry into force of the Act.

The Chief Executive compared this measure to the PP's cuts that "more than 175,000 people were expelled from the system" and stressed that "the progressive government is making progress in both financing and the quality of the dependency system."

"For a country that looks after everyone, we continue to advance rights," Sanchez reiterated in his publication.

 

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