Living with haemophilia and von Willebrand's: A descriptive qualitative study
| Autor: | David R. Ellard, Jacqueline Stapley, Julie H. Barlow |
|---|---|
| Rok vydání: | 2007 |
| Předmět: |
Adult
Male congenital hereditary and neonatal diseases and abnormalities medicine.medical_specialty Comorbidity Hemophilia A Haemophilia Interviews as Topic Social support hemic and lymphatic diseases Health care Humans Medicine Family Psychiatry Qualitative Research Aged Aged 80 and over business.industry Social Support General Medicine Middle Aged medicine.disease Family life von Willebrand Diseases Anxiety Female Thematic analysis medicine.symptom business Prejudice Qualitative research |
| Zdroj: | Patient Education and Counseling. 68:235-242 |
| ISSN: | 0738-3991 |
| DOI: | 10.1016/j.pec.2007.06.006 |
| Popis: | Objective The aim of this qualitative descriptive study was to describe the experience of living with bleeding disorders and to identify the associated salient issues from the perspectives of people living with haemophilia or von Willebrand's Disease (vWD). Methods Nine members of The Haemophilia Society took part in a semi-structured interview. The interviews were tape recorded and transcribed and the results subjected to thematic content analysis. Results Participants described the physical aspects of their condition, such as bleeding into joints, the implications of bleeds and development of co-morbid conditions (e.g. arthritis). Many felt that their bleeding disorder had impacted on their education, work, social activities and family life. Anxiety and depression were associated with daily management of symptoms, the unpredictable nature of bleeding disorders and concerns about the future. All participants had encountered a degree of stigmatisation related to their condition and felt that there was a public misconception about bleeding disorders. Many had experienced discrimination in educational and work settings. Some participants expressed a preference for seeking treatment from specialist services. Conclusion Living with haemophilia and vWD poses a number of daily and longer-term challenges not only for individuals, but also for their families. Further investigation of ways to support such individuals is warranted. Practice implications Greater awareness and understanding of the issues faced by people living with haemophilia and vWD is needed for the general public, employers, and healthcare staff, particularly those working in Accident and Emergency Departments. |
| Databáze: | OpenAIRE |
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