Understanding Bleeding Disorders

About Bleeding Disorders

Bleeding disorders disrupt the blood clotting process, leading to prolonged bleeding and potential complications. From hemophilia to von Willebrand disease and rare clotting factor deficiencies, these conditions impact individuals worldwide, highlighting the need for awareness and support.

What is Hemophilia?

Hemophilia, an inherited bleeding disorder, results in deficient clotting factor levels, leading to prolonged bleeding. Hemophilia A and B, along with von Willebrand disease, represent the most prevalent forms, each with its unique challenges and management approaches.

Who is Affected by Hemophilia?

Hemophilia transcends race and ethnicity, affecting individuals irrespective of background. While severe forms primarily impact males, carriers and rare genetic occurrences can lead to symptomatic presentations in females. Early diagnosis is critical, with most cases identified in infancy or early childhood.

Understanding the Severity

Classified as severe, moderate, or mild, hemophilia's severity correlates with factor VIII or IX levels in the blood. Severe cases, characterized by less than 1% of normal clotting factor levels, often lead to frequent and spontaneous bleeds, posing significant health risks without proper management.

Causes of Bleeding

Bleeding episodes in hemophilia are often triggered by minor trauma or occur spontaneously, especially in joints with a history of bleeding. Brain hemorrhages, a severe complication, underscore the importance of prompt recognition and intervention to prevent life-threatening outcomes.


As we commemorate World Hemophilia Day, let us stand in solidarity with the global bleeding disorders community, advocating for equitable access to care and support. Together, we can break barriers, raise awareness, and pave the way for a future where everyone, regardless of their bleeding disorder, can thrive.


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