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Sunday, April 17, 2016

World Hemophilia Day - April 17


Supported by the World Federation of Hemophilia (WFH), hemophilia awareness day was first established in 1989.

The date of 17th April was chosen to honor Frank Schnabel the founder of WFH, whose birthday falls on the same date

Hemophilia is a condition in which bleeding is prolonged.

Hemophilia is a condition present from birth and is normally inherited; you can't 'catch' hemophilia or pass it onto others.

 In some rare instances, hemophilia may develop later in life (typically affecting people in the 50+ age group)

The incidence of hemophilia is quite low. Statistics on the incidence of hemophilia vary however, its estimated that in the United States 1 in every 5,000 -10,000 people are born with it.
 
When a person without hemophilia bleeds, normal levels of clotting factor, a protein in the blood, causes the blood to clot and stops the bleeding. However, hemophiliacs (people with hemophilia) have lower levels of clotting factor in the the blood and bleeding continues for much longer periods.

There are two types of hemophilia.

Each type is linked to a low level of a certain clotting factor.

Hemophilia A is the more common type and is linked to low levels of clotting factor VIII (8).

Hemophilia B is more rare and is associated with low levels of clotting factor IX (9).

 Hemophilia is diagnosed by taking a blood sample and testing the levels of clotting factor VIII & IX.

Each type of hemophilia causes prolonged bleeding which is the main symptom of hemophilia.

Bleeding can range from mild to severe. Bleeding is often internal, although people can bleed outside the body too.

Other symptoms include spontaneous bleeding, bleeding into the muscles or joints, bleeding for a prolonged period after having surgery, having a cut or dental work, and big bruises.

In very mild cases, bleeding may be for a shorter duration and only arise after injury or surgery.

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