ALS patients urge the Government: “More than 213 patients have died without care with a law in force”
Patients ask that the development of the new regulations be accelerated Meeting of representatives of ALS patients with ministers Mónica ...
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He suffers from ALS and has been waiting for almost a year for an increase in dependency assistance and disability review
María del Carmen is 53 years old, lives in Las Palmas de Gran Canaria and for several years she started ...
Congress disgraces the Government for not financing the ALS law
A little over two months ago, patients with amyotrophic lateral sclerosis celebrated in the Congress of Deputies the unanimity by ...
ALS patients report that they continue without help despite the entry into force of the law
A month and a half after the Official State Gazette (BOE) published the ALS law, the text that regulated aid ...
Victims of abuse demand ‘an ELA pact’ so that sexual crimes against minors do not prescribe: “This is not about the left or the right”
The so-called Children's Law, renamed the Rhodes Law due to the sexual abuse suffered by the British pianist based in ...
Kamala Harris closes her campaign in Philadelphia with an optimistic message: “Yes, she can”
In front of a staircase symbol of resistance, Kamala Harris closed her campaign this Monday with a call for the ...
The BOE publishes the ELA law, which will come into force with its financing in the air
After years of waiting and pleading, patients with amyotrophic lateral sclerosis (ALS) finally see this Thursday how their request has ...
The terminal cancer of an Olympic champion and the heartbreaking message from his wife, sick with ALS
At the end of last year, Chris Today He went to the doctor because of the constant pain he was ...
Researcher Guadalupe Sabio and ALS patients, ABC Salud 2024 awards
The researcher Guadalupe Sabio (Badajoz 1977) was going to become a veterinarian until she discovered that her thing was the ...
The speech of Senator Juan Ramón Amores, suffering from ALS, to celebrate the law: “I will not rest until it reaches everyone who needs it”
The law that aims to improve the quality of life of people with amyotrophic lateral sclerosis (ALS) saved its last ...
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