References
- 1. Evatt BL. The natural evolution of haemophilia care: developing and sustaining comprehensive care globally. Haemophilia 2006; 12: 13-21. doi: 10.1111/j.1365-2516.2006.01256.x
- 2. Pollard D, Moore J. What is the impact on quality of life of living with severe haemophilia. J Haem Pract 2016; 3(1). doi: 10.17225/jhp00068
- 3. Alavian S, Norton C, Othman S. Living with mild haemophilia and care following a bleed - a qualitative study. J Haem Pract 2016; 3(1). doi: 10.17225/jhp00063
- 4. Rambod M, Sharif F, Molazem Z, Khair K. Pain: the voiceless scream in every haemophilia patient’s life. J Haem Pract 2016; 3(1). doi: 10.17225/jhp00061
- 5. Broyles LM, Binswanger IA, Jenkins JA, Finnel DS, Faseru B, Cavaiola A, Pugatch M, Gordon AJ. Confronting inadvertent stigma and pejorative language in addiction scholarship: a recognition and response. Substance Abuse 2014; 35:3: 217-221. doi: 10.1080/08897077.2014.930372
- 6. Monsivais, D. Decreasing the stigma burden of chronic pain. Journal of American Association of Nurse Practitioners 2013; 25: 551-556.10.1111/1745-7599.12010
- 7. Riley RR, Witkop M, Hellman E, Akins S. Assessment and management of pain in haemophilia patients. Haemophilia 2011; 17(6): 839-45. doi: 10.1111/j.1365-2516.2011.02567.x.2516.2011.02567.x.