Literature DB >> 19955225

"All at sea": the experience of living with cystic fibrosis.

Melanie Jessup1, Camillus Parkinson.   

Abstract

In this qualitative study the researchers explored living with cystic fibrosis (CF)-a chronic, life-threatening, life-limiting disease that demands a relentless regime of daily treatment. The unique challenges and issue for care that CF presents were considered. Utilizing a phenomenological perspective, data drawn from unstructured interviews included narratives and drawings contributed by children, adolescents, young adults, and parents-eight families representing nine young people with CF. In line with van Manen's approach, four existentials were used to consider a lifeworld in which notions of time, body, space, and relationship are indelibly altered. From original fright, through ongoing dynamics of fear, fight, flight, form, familiarity, and philosophy, people with CF pursue a future that is threatened and continually redefined. As a result of enhanced understanding, care can be delivered from an empathetic bearing toward those for whom it is not so much a bothersome routine, but a life-and-death imperative.

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Year:  2009        PMID: 19955225     DOI: 10.1177/1049732309354277

Source DB:  PubMed          Journal:  Qual Health Res        ISSN: 1049-7323


  9 in total

1.  Hoping to live a "normal" life whilst living with unpredictable health and fear of death: impact of cystic fibrosis on young adults.

Authors:  Lorraine Higham; Shenaz Ahmed; Mushtaq Ahmed
Journal:  J Genet Couns       Date:  2012-12-14       Impact factor: 2.537

2.  "Basically, You Had Cancer and Now You Don't": Exploring the Meaning of Being a "Cancer Survivor" Among Adolescents and Young Adult Cancer Survivors.

Authors:  Katie Darabos; Jennifer S Ford
Journal:  J Adolesc Young Adult Oncol       Date:  2020-04-02       Impact factor: 2.223

3.  It's About Time: The Temporal Burden of Lower Urinary Tract Symptoms Among Women.

Authors:  Beverly Rosa Williams; Keith Vargo; Diane K Newman; D Yvette Lacoursiere; Elizabeth R Mueller; John Connett; Lisa Kane Low; Aimee S James; Ariana L Smith; Kathryn H Schmitz; Kathryn L Burgio
Journal:  Urol Nurs       Date:  2020 Nov-Dec

4.  Family-centred care in cystic fibrosis: a pilot study in North Queensland, Australia.

Authors:  Wendy Smyth; Gail Abernethy; Melanie Jessup; Tonia Douglas; Linda Shields
Journal:  Nurs Open       Date:  2017-05-11

5.  The lived experience of adults with cystic fibrosis: what they would tell their younger selves about the gut.

Authors:  L Cave; L J Milnes
Journal:  J Hum Nutr Diet       Date:  2019-11-25       Impact factor: 3.089

6.  A meta-ethnographic study of fathers' experiences of caring for a child with a life-limiting illness.

Authors:  Gianina-Ioana Postavaru; Helen Swaby; Rabbi Swaby
Journal:  Palliat Med       Date:  2020-12-18       Impact factor: 4.762

7.  "The Stakes Are Higher"- Patient and Caregiver Perspectives on Cystic Fibrosis Research and Personalized Medicine.

Authors:  Terese Knoppers; Marie Cosquer; Julie Hagan; Minh Thu Nguyen; Bartha Maria Knoppers
Journal:  Front Med (Lausanne)       Date:  2022-03-23

8.  Impact of pulmonary exacerbations and lung function on generic health-related quality of life in patients with cystic fibrosis.

Authors:  Caitlyn T Solem; Montserrat Vera-Llonch; Sizhu Liu; Marc Botteman; Brenda Castiglione
Journal:  Health Qual Life Outcomes       Date:  2016-04-21       Impact factor: 3.186

9.  Associations between adherence, depressive symptoms and health-related quality of life in young adults with cystic fibrosis.

Authors:  K B Knudsen; T Pressler; L H Mortensen; M Jarden; M Skov; A L Quittner; T Katzenstein; K A Boisen
Journal:  Springerplus       Date:  2016-07-29
  9 in total

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