To call upon government officials and local policy makers to promote better control and prevention of hemophilia as well as provision of better treatment and care.
Theme: “Equitable access for all: recognizing all bleeding disorders”.
Emphasizes treatment for all and envisions a society in which every person with hereditary bleeding disorders has access to care, regardless of their bleeding status, sex, age, or location.
History:
In 1803, Dr. John Conrad Otto of Philadelphia began researching "bleeders", eventually concluding that the disease was transmitted from mothers to sons.
In 1937, hemophilia was classified as a type A or B genetic disorder.
World Haemophilia Day was first observed on 17 April 1989 by the World Federation of Haemophilia (WFH) to honor the birthday of WFH founder Frank Schnabel.
Significance:
Bringing together individuals, organizations and health care professionals to raise awareness of hemophilia and its impact on the lives of those affected.
It provides an opportunity to educate the public about the condition, its symptoms and available treatments.
It serves as a platform to advocate for better diagnosis, accessible care, and prevention strategies for individuals with bleeding disorders.
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