How hemophilia affects your life?

How hemophilia affects your life?

Hemophilia can result in: Bleeding within joints that can lead to chronic joint disease and pain. Bleeding in the head and sometimes in the brain which can cause long term problems, such as seizures and paralysis. Death can occur if the bleeding cannot be stopped or if it occurs in a vital organ such as the brain.

What limitations does a person with hemophilia have?

Severe limitations in range of motion, chronic pain, and crippling disability are the ultimate outcomes for many patients who experience chronic hemophilic arthropathy. Hematomas, another complication of hemophilia, generally do not arise spontaneously.

How does hemophilia affect the body and joints?

Advertisement. Hemophilia causes bleeding and bruising. This can lead to internal bleeding and painful swelling of the joints. Septic arthritis occurs more frequently in people with hemophilia.

Can a person with hemophilia have a fulfilling life?

About 25 percent of young people with severe hemophilia — those between the ages of 6 and 18 — have below-normal motor skills, academic performance, and emotional and behavioral problems. With appropriate education and treatment, people with hemophilia can have fulfilling and productive lives, however.

How many people die each year from hemophilia?

About 70 percent of those with hemophilia have the severe form. The most important life-threatening complications of the disease are bleeding in the skull and hemorrhages in soft tissue around airways or other internal organs. About 10 percent of those with severe hemophilia have bleeding in the skull, and 30 percent with the condition die.

How does a person with hemophilia stop bleeding?

About 15-20 percent of people with hemophilia develop an antibody (called an inhibitor) that stops the clotting factors from being able to clot the blood and stop bleeding.

What is the life expectancy of someone with hemophilia?

Life expectancy in hemophilia varies, depending on whether patients receive appropriate treatment. Many patients still die before adulthood due to inadequate treatment. With proper treatment, life expectancy is only about 10 years less than healthy men.

What are the risk factors of hemophilia?

However, recent evidence suggests that hemophilia patients can suffer from atherosclerosis, or plaques in the arteries, at a similar rate as the general population. Furthermore, risk factors that contribute to cardiovascular disease, such as hypertension, or high blood pressure, are frequently present in men with severe hemophilia.

What is the current treatment for hemophilia?

The current, most-used treatment for hemophilia A is factor replacement therapy. This is done by infusing (giving medication into a vein) a FVIII product into the affected person.

What are the effects of hemophilia?

Hemophilia mainly affects joints and muscles causing spontaneous bleeding after an injury or cut. Person with hemophilia can experience extended bleeding along with bruising leading to inflamed joints. Digestive problems and abdominal bleeding are the common concerns in people with hemophilia.