Awarded/Presented
Tags
Bleeding Disorders Conference
Psychosocial Issues
Researchers
Michelle Witkop, Sarah Hawk, Angela Lambing, Chris Guelcher, Randall Curtis, Neil Frick, Laureen Kelley, Michelle Rice, David Cooper

Objective:

To assess impact of hemophilia on relationships and employment during the transition to adulthood in young adult (YA) patients with hemophilia (PWH).

Methods:

Analysis of US YA-PWH respondents (aged 18-30 years) in the HERO study.

Summary:

Of 189 US adult PWH HERO respondents, 66 were aged 18-30 years (median: 26). Most lived in large cities (52%) or suburban areas (29%); 73% reported household income of <$60,000/year. Some (32%) were married or in long-term relationships; 20% lived alone. Negative impact on relationships was reported by 32%; 62% predicted an impact in the future, 62% cited difficulty understanding issues, and 52% worry about supporting a family. Only 9% had children; 77% wanted to have children. Only 45% received genetic counseling from the HTC; of those, 60% felt it was helpful. Most were very/quite satisfied with support of partners/spouses (95%), family (92%), and friends (86%). Negative reactions telling friends were reported by 41%; 59% reported most/all of their friends knew about their hemophilia. Most (78%) were employed with 57% reporting office work. One fifth (20%) reported being disabled, and 14% received disability benefits. The majority (74%) reported negative impact on employment; 39% reported moderate/very large impact. Many (43%) reported current treatment allows them to work in most situations, 37% selected a job based on their needs, 29% were helped to obtain a job, 24% had to leave a job, 20% were not hired, and 18% lost a job due to hemophilia. Only 36% received advice from the HTC on work/employment, mostly on what to do if a bleed occurs at work (71%), suitable jobs (67%), when (63%) and what (33%) to tell an employer, and workplace precautions (46%). Fifty-eight percent found the advice helpful. Only 37% reported most/all of their colleagues know about their hemophilia; 38% reported a select few or 1-2 and 26% none. Most were very/quite satisfied with the support of colleagues at work/school (82%). Most YA-PWH (62%) were members of an organization or online (48%) or other (35%) support group.

Conclusions:

During the transition to independent adults, YA-PWH are likely planning for family and careers. Many reported negative impacts on relationships and employment, highlighting a need for career counseling. YA-PWH are supported by friends and colleagues, but this may be a limited group. HTCs are an underutilized resource for addressing these issues, with perhaps online peer-support networks playing a larger role during this transition to adulthood and independence.