Search

A recent study conducted by the University of Milano Bicocca in Italy examined the psychosocial impact of haemophilia on patients and caregivers. The study found that adult patients with haemophilia reported significant impairments in various psychosocial aspects, including work, family relationships, and social interactions. Caregivers generally reported better scores in all aspects of the survey. The study also highlighted the importance of genetic counseling and psychological support for patients and caregivers, as many respondents reported a lack of awareness and support in these areas. Overall, the study provides updated insights into the psychosocial challenges faced by individuals with haemophilia and their caregivers in the context of evolving treatment strategies. [Extracted from the article]