The Hajar association, a Moroccan non-profit, is actively working to support children suffering from primary immunodeficiencies (PID), a group of rare genetic disorders that impair the immune system. As of May 2026, the organization continues to raise awareness and provide assistance to affected families.
Primary immunodeficiencies are often underdiagnosed in Morocco, leading to delayed treatment. The Hajar association focuses on early detection, access to specialized care, and financial aid for medical expenses. They also organize educational campaigns for healthcare professionals and the public.
According to the association's recent reports, they have helped dozens of children receive immunoglobulin therapy and bone marrow transplants, which are critical for managing these conditions. The group collaborates with hospitals and international experts to improve outcomes.
Despite challenges, the Hajar association remains committed to its mission, advocating for better healthcare policies and support for rare disease patients in Morocco.
