Affiliation:
1. Medical writer , Haemnet , UK .
2. Director of Research , Haemnet , UK
Abstract
Abstract
Women who have the gene variant for haemophilia are labelled solely as ‘carriers’ unless they have a factor VIII activity of ≤40%. This term, which describes an individual who can pass on a disorder but are themselves unaffected, reflects a legacy that extends from the 18th century to the present day. There is strong evidence that women labelled as carriers experience heavy periods, joint damage, pain and impaired quality of life. The label ‘carrier’ does not recognise this burden and is associated with guilt, stigma and difficulty accessing care. People living with a long-term disorder should now be described using person-first terminology and it is common to see the term ‘people with haemophilia’. The term ‘carrier’ should be limited to its application in genetics and not used as a catch-all label for women with haemophilia.
Reference33 articles.
1. Otto JC. An account of an hemorrhagic disposition existing in certain families. The Medical Repository and Review of American Publications on Medicine, Surgery and the Auxiliary Branches of Science 1803; 6:1–4.
2. Hay J. Account of a remarkable hæmorrhagic disposition, existing in many individuals of the same family. New Engl J Med 1813; 2: 221–5. doi: 10.1056/NEJM181307010020302.
3. Watson T. Lecture XV: Hæmorrhage. In Lecture on the Principles and Practice of Physic. The fourth edition, revised and enlarged. London: John W. Parker and Son, I857. Vol. 1, 254–255. Available from https://books.google.co.uk/books/about/Lectures_on_the_Principles_and_Practice.html?id=5jxAAAAAYAAJ&redir_esc=y (accessed 29 September 2021).
4. Bemiss JH. Haemophilia. New Orleans Medical and Surgical Journal 1884; September: 165–178.
5. Rushton AR. Leopold: the “bleeder prince” and public knowledge about hemophilia in Victorian Britain. J Hist Med Allied Sci 2012; 67: 457–90. doi: 10.1093/jhmas/jrr029.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献