Giugno 2012 - Volume XXXI - numero 6

Medico e Bambino


Articolo speciale

Nostro figlio ha una malattia metabolica rara

Riccardo Rubessa1, Flavio Bertoglio2, Franca Parizzi3, Francesca Furlan4,5, Francesca Santus5, Francesca Nichelli6, Rossella Parini5, Giuseppe Masera7

1Presidente dell’Associazione per la tutela del bambino con malattie metaboliche (ABM); 2Presidente dell’Associazione Italiana Mucopolisaccaridosi e Malattie Affini (AIMPS); 3Pediatra, Consiglio Direttivo della Società Italiana di Pedagogia Medica (SIPeM); 4Responsabile del Progetto, 5Medici referenti dell’ABM e dell’AIMPS, 6Psicologa, 7Professore di Pediatria,
Clinica Pediatrica dell’Università di Milano-Bicocca, Ospedale San Gerardo di Monza

Indirizzo per corrispondenza: g.masera@hsgerardo.org

Our child suffers from a rare metabolic disease

Key words: Narrative medicine, Metabolic disorders, Therapeutic alliance, Resilience

Genetic metabolic disorders are multiorgan complex diseases, with only partially effective treatment available. Two families associations (Associazione per la tutela del bambino con malattie metaboliche “ABM” and Associazione Italiana Mucopolisaccaridosi “AIMPS”) collected 8 narratives that were later analyzed by the health workers involved in this project. In this paper the personal experience of parents is reported, from the critical time of diagnosis, through the acceptance and processing of information related to the disease, to the need of explaining the disease to the child and the other children in the family. Practical matters are also approached, like the difficult contact with the Regional Health Service and the major need of care of these special children, requiring the attention of one of the parents who often abandons her/his job. This kind of experience is behind the current medical practice and allows the doctors to better understand which are the unmet needs of the parents/families in order to improve the standard care and the quality of life of the patients/families.

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R. Rubessa, F. Bertoglio, F. Parizzi, F. Furlan, F. Santus, F. Nichelli, R. Parini, G. Masera Nostro figlio ha una malattia metabolica rara. Medico e Bambino 2012;31(6):371 https://www.medicoebambino.com/?id=1206_371.pdf


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