Literature DB >> 10672092

Family members' experience of familial amyloidotic polyneuropathy disease--an infernal struggle and a fact of life.

E Jonsén1, E Athlin, O B Suhr.   

Abstract

Familial amyloidotic polyneuropathy is a fatal, hereditary, systemic, progressive amyloidosis. No previous qualitative study of the family members' experience of the disease has been published. The purpose of this phenomenological study was to understand the lived experience of family members whose nearest and dearest suffered from familial amyloidotic polyneuropathy. In-depth interviews were conducted with six family members. The analysis of the data was inspired by Colaizzi's method. Two major theme categories, difficult to accept and forced to accept, emerged from the interviews. Implications for nursing practice, such as genetic counselling and support, are discussed.

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Year:  2000        PMID: 10672092     DOI: 10.1046/j.1365-2648.2000.01291.x

Source DB:  PubMed          Journal:  J Adv Nurs        ISSN: 0309-2402            Impact factor:   3.187


  3 in total

1.  Death anxiety and symbolic immortality in relatives at risk for familial amyloid polyneuropathy type I (FAP I, ATTR V30M).

Authors:  Paula I Santos; Eurico Figueiredo; Inês Gomes; Jorge Sequeiros
Journal:  J Genet Couns       Date:  2010-08-03       Impact factor: 2.537

2.  Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy.

Authors:  Lorenza Magliano; Laura Obici; Claudia Sforzini; Anna Mazzeo; Massimo Russo; Francesco Cappelli; Silvia Fenu; Marco Luigetti; Matteo Tagliapietra; Chiara Gemelli; Luca Leonardi; Stefano Tozza; Luca Guglielmo Pradotto; Giulia Citarelli; Alessandro Mauro; Fiore Manganelli; Giovanni Antonini; Marina Grandis; Gian Maria Fabrizi; Mario Sabatelli; Davide Pareyson; Federico Perfetto; Giampaolo Merlini; Giuseppe Vita
Journal:  Orphanet J Rare Dis       Date:  2021-04-07       Impact factor: 4.123

3.  Health-related quality of life in hereditary transthyretin amyloidosis polyneuropathy: a prospective, observational study.

Authors:  Mónica Inês; Teresa Coelho; Isabel Conceição; Lara Ferreira; Mamede de Carvalho; João Costa
Journal:  Orphanet J Rare Dis       Date:  2020-03-06       Impact factor: 4.123

  3 in total

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