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Mattarella, no disease is ever so rare that it doesn't deserve treatment - Last hour

2024-02-29T09:14:09.678Z

Highlights: Mattarella, no disease is ever so rare that it doesn't deserve treatment - Last hour. In Italy there are more than two million people affected by diseases of this nature. World Rare Diseases Day draws attention to this particularly difficult condition. It is     necessary to increase investments in research and encourage a multidisciplinary approach in order to identify effective and rapid diagnostic and treatment paths. The approval of the "National Rare Diseases Plan 2023-2026", which took place last May, represents a step forward towards those who ask for concrete solutions.


"Every disease evokes conditions of fragility, sometimes of isolation, particularly in the case of rare diseases, which present difficulties in diagnosis and therapeutic approach, as well as significant burdensome care and management of patients, even... (ANSA)


"Every disease evokes conditions of fragility, sometimes of isolation, particularly in the case of rare diseases, which present difficulties in diagnosis and therapeutic approaches, as well as significant burdensomeness in the treatment and management of patients, also due to insufficient investments in the sector of pharmaceutical research and experimentation. In Italy there are more than two million people affected by diseases of this nature.


    World Rare Diseases Day draws attention to this particularly difficult condition. Continuous progress in personalized medicine, genomic and biomedical technologies offer new treatment possibilities for various pathologies, opening up the path to more targeted and effective therapies and making the future of many people affected by rare diseases increasingly encouraging, provided that the community is able to take responsibility for the right to health of these citizens. It is


    necessary to increase investments in research and encourage a multidisciplinary approach in order to identify effective and rapid diagnostic and treatment paths.

The approval of the "National Rare Diseases Plan 2023-2026", which took place last May, represents a step forward towards those who ask for concrete solutions to improve the quality of their lives, because no disease is ever too rare to deserve an effective treatment".


    And ' the message of the President of the Republic, SergioMattarella, on the occasion of World Rare Diseases Day.


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Source: ansa

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