The PP brings a motion to the Senate to guarantee the budgetary endowment of the ELA Act

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The National Confederation of Amyotrophic Lateral Sclerosis Entities (CONELA) has expressed its concern about the lack of progress in the implementation of the ALS Law, published on October 31, 2024 and in force since the following day. More than 100 days later, people affected by ALS and their families continue to lack clear answers or […] The entry CONELA calls for urgent action for the effective implementation of the ALS Law appeared first on…

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The PP has filed a motion in the Senate urging the government to "not leave the patients of the commonwealth homeless" and to guarantee, "without further delay", the necessary budget allocation to ensure the full implementation of all the advances envisaged in Law 3/2024 to improve the quality of life of people with Amyotrophic Lateral Sclerosis and other diseases or processes of high complexity and irreversible course.