HAL is a non-profit organisation supporting people with haemophilia and related inherited bleeding disorders in Lesotho. The association works with families, healthcare providers, public institutions and partners to improve awareness, diagnosis, treatment access and long-term care.
Who we serve
HAL supports people with haemophilia, von Willebrand disease, platelet function disorders, other rare bleeding conditions, family members and caregivers. The organisation also engages schools, health facilities and communities so that suspected cases can be identified earlier and referred for care.
Our approach
- Raise awareness about bleeding disorder symptoms and care needs.
- Advocate for equitable access to diagnosis and treatment.
- Train and support healthcare workers, teachers and community leaders.
- Build partnerships with national, regional and global stakeholders.
- Empower members and families through education and peer support.
Members
Members are central to HAL’s work. Their lived experience guides advocacy, outreach, education and service improvement. This page can later include membership registration details, benefits and downloadable forms.