Literature DB >> 12010452

The impact of chronic disease on the family.

G Goldstein1, G Kenet.   

Abstract

Haemophilia is a chronic disease, affecting patients and their families. The impact of such a disease upon each family is dependent upon family type and characteristics and adjustment to it varies with time, in concordance with the family's lifecycle. In the National Hemophilia Center in Israel we lead a special support system and conduct group therapy from the very early stage of haemophilia diagnosis throughout the lifetime of patients. The general definitions of a family's lifecycle, the effect of the disease and the required adjustment to it are described in this paper. We refer to special difficulties associated with haemophilia as a chronic, genetic disease and describe ways to cope, discussing the support systems that have been established in our centre.

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Year:  2002        PMID: 12010452     DOI: 10.1046/j.1365-2516.2002.00642.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  6 in total

1.  Understanding of genetic inheritance among Xhosa-speaking caretakers of children with hemophilia.

Authors:  Gabriele Solomon; Jacquie Greenberg; Merle Futter; Lauraine Vivian; Claire Penn
Journal:  J Genet Couns       Date:  2012-03-10       Impact factor: 2.537

2.  "It was a lot Tougher than I Thought It would be". A Qualitative Study on the Changing Nature of Being a Hemophilia Carrier.

Authors:  Charlotte von der Lippe; Jan C Frich; Anna Harris; Kari Nyheim Solbrække
Journal:  J Genet Couns       Date:  2017-05-26       Impact factor: 2.537

Review 3.  Hemophilia Care in the Pediatric Age.

Authors:  Marta Bertamino; Francesca Riccardi; Laura Banov; Johanna Svahn; Angelo Claudio Molinari
Journal:  J Clin Med       Date:  2017-05-19       Impact factor: 4.241

Review 4.  The experiences and attitudes of hemophilia carriers around pregnancy: A qualitative systematic review.

Authors:  Marieke C Punt; Tanja H Aalders; Kitty W M Bloemenkamp; Mariette H E Driessens; Kathelijn Fischer; Marlies H Schrijvers; Karin P M van Galen
Journal:  J Thromb Haemost       Date:  2020-05-12       Impact factor: 5.824

5.  Health care professionals dealing with hemophilia: insights from the international qualitative study of the HERO initiative.

Authors:  Silvia Potì; Laura Palareti; Frederica Rmy Cassis; Sonia Brondi
Journal:  J Multidiscip Healthc       Date:  2019-05-09

6.  Parental experiences of having a child with CLN3 disease (juvenile Batten disease) and how these experiences relate to family resilience.

Authors:  Mattias Krantz; Emma Malm; Niklas Darin; Kalliopi Sofou; Antri Savvidou; Colin Reilly; Petra Boström
Journal:  Child Care Health Dev       Date:  2022-03-04       Impact factor: 2.943

  6 in total

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