Spouses & Partners
Spouses/Partners
Hemophilia, von Willebrand Disease and other bleeding disorders are chronic conditions that impact the entire family, spouses and partners included.
Are you a partner to someone with a bleeding disorder? Would you like an opportunity to network with others in similar relationships to your own? Would you like support from others who know what it’s like to love someone with a bleeding disorder? Could you benefit from efforts to raise awareness about the realities of living and loving in the face of a bleeding disorder? If you answered “YES”, please join us.
How to Connect with other Partners and Spouses in the community:
- Join the Partners and Spouses Private Group on HFA’s Online Community – a place to learn and support one another
- Participate in Partners and Spouses National Webinars (HFA Calendar of Events)
- Encourage other spouses and partners to join the network and spread the support!
Join HFA’s network for Spouses and Partners in the bleeding disorders community!
Stories of People with Bleeding Disorders
For more information contact hfaprograms@hemophiliafed.org.