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Als, a Reality of Dramatic Numbers and Rights All Too Often Denied
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Dear Director, I write to you not only as a citizen, but as a sister of a man who fights every day against the Amiotrophic Lateral Sclerosis (SLA). I do so on behalf of a group of patients and family members who, together with the lawyer Fabio Trapuzzano of Lamezia Terme (Cz), have signed a heartfelt appeal addressed to the Ministry of Health and the Conference of the Regions. ALS is not only a diagnosis; it is a reality made of dramatic numbers…
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