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A toddler playing in the fountain at a park in Santa Fe, New Mexico—Photo LD Lewis. In August, we live through the Dog Days of Summer. It's hot and often humid, and those ...
Can you hear that sigh of relief from parents worldwide? Yes! September marks the return of students to school, a global phenomenon. Preparations for the ACT and SATs begin earnestly for ...
October is the busiest month for events, with 5% more happening than in May, the second most eventful month. Sailing enthusiasts will be glued to the finals of this year's Am...
Bleeding Disorders Awareness Month, formerly Hemophilia Awareness Month, focuses on the genetic blood disease that prevents blood from clotting usually. Due to its prevalence in monarchies, Hemophilia earned the nickname "Royal Disease."
Queen Victoria of England (1837-1901) was a carrier of the hemophilia gene. Her eighth child Leopold suffered from frequent bleeding, which was reported in the British Medical Journal in 1868.
Hemophilia has been known for thousands of years. The Talmud, a collection of Jewish rabbinical writings from the second century of the Common Era, notes exempts male babies from circumcision if two brothers had already died from the procedure.
By the 1990s, the safety and efficacy of factor concentrate improved.
In 1992, the first recombinant factor VIII product received approval from the Food and Drug Administration (FDA).
In 1997, factor IX products captured FDA approval. Additional synthetic drugs, including desmopressin acetate (DDAVP), which treat mild-to-moderate Hemophilia A and Von Willebrand disease, also were introduced.
By the mid-1990s, prophylactic (a preventative treatment regimen) therapy in children with hemophilia became more common. Since the advent of prophylaxis, children could look forward to a life of less pain due to chronic bleeding.
Today, hemophiliac children attain long, healthy, and active lives.
This event first occurred in 1986.
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