+266 2231 0522 info@haemophilia.org.ls P.O. Box 1419, Maseru 100, Lesotho
LETS SCREEN AND DIAGNOSE HAEMOPHILIA
Treatment for all

Better bleeding disorder care for Lesotho

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.

Awareness Advocacy Outreach Capacity building
HAL logo Treatment, dignity and community care Connecting people to information, support and advocacy.
2004 Serving the bleeding disorders community
WFH Part of a global care movement
HAL community group
Who we are

A stronger community, a better future

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.

  • We advocate for safe and effective treatment access.
  • We support early diagnosis and better public awareness.
  • We work with health facilities, families and communities.
  • We strengthen capacity through training and partnerships.
More About Us
Core focus areas

Built around care, access and dignity

The site has been structured around the main journeys visitors need: learning, finding help, understanding HAL’s work and connecting with the organisation.

01

Education & Awareness

Simple information for patients, families, schools, communities and healthcare workers.

02

Treatment Advocacy

Clear advocacy for diagnosis, treatment access and specialised care for bleeding disorders.

03

Rural Outreach

Support for communities that face distance, cost and awareness barriers to proper care.

04

Partnerships

Collaboration with government, public and private sector partners, health teams and donors.

1000+ Patients & families supported
30+ Health facilities reached
50+ Awareness & outreach activities
20+ Partners & supporters