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Thalassemia ReportsThalassemia Reports
  • Thalassemia Reports is published by MDPI from Volume 12 Issue 1 (2022). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with PAGEPress.
  • Brief Report
  • Open Access

4 December 2014

Are We Strong Enough to Assert Our Rights in Quality Healthcare?

1
Thalassaemia International Federation (TIF), Strovolos, Cyprus
2
Associazione Ligure Thalassemici Onlus, Via Alessandro Volta, 8, 16128 Genova GE, Italy

Abstract

The title of this speech is an important challenge for me, for a patient I mean, to face because it’s not easy to state today if we are really strong enough to assert our rights for a quality healthcare. At first sight, and in an optimistic vision, we could answer to this question YES, we are, but I think we need to explore better the field before to confirm that this is the right answer to the question. The first thing to assess is what we mean with the pronoun WE: the patients and parents’ community represented from TIF? The whole community that plays around thalassemia and hemoglobinopathies, meaning patients and parents and scientists? What else?

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