Education & Awareness
Simple information for patients, families, schools, communities and healthcare workers.
HAL works with families, health workers, partners and communities to improve awareness, diagnosis, treatment access and support for people living with haemophilia and related inherited bleeding disorders.
Treatment, dignity and community care
Connecting people to information, support and advocacy.
Learn about haemophilia, Von Willebrand disease, inhibitors, prophylaxis and other bleeding conditions.
Explore disorders →See HAL’s work in awareness, advocacy, outreach and capacity building across Lesotho.
View programmes →Meet the leaders, advisory members and volunteers supporting HAL’s mission.
Meet the team →Contact HAL for guidance, referrals, awareness information and partnership opportunities.
Contact us →
The Haemophilia Association of Lesotho is a non-profit organisation dedicated to improving the quality of life for people with bleeding disorders in Lesotho through education, advocacy, partnerships and community support.
The site has been structured around the main journeys visitors need: learning, finding help, understanding HAL’s work and connecting with the organisation.
Simple information for patients, families, schools, communities and healthcare workers.
Clear advocacy for diagnosis, treatment access and specialised care for bleeding disorders.
Support for communities that face distance, cost and awareness barriers to proper care.
Collaboration with government, public and private sector partners, health teams and donors.
Keep track of HAL events, awareness programmes, camps, trainings and partnership activities.
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