0
The quality of life for a person with hemophilia has grown by leaps and bounds throughout the past 50 or so years. Severe hemophiliacs for example that were born in the 30s often died before the age of 20 and would have many deformed joints preventing them from enjoying many things.
As treatments improved, bleeding disorders became a chronic condition and life expectancy became almost the same as the rest of the population. Because the treatment was only given when the individual already had a bleeding episode, joint damage and deformities were common and the patients had to spend a good deal of time in the hospital.
In the late 80s and early 90s, as treatment became even better and the extensive joint damage was lessoning, diseases contaminated the blood supply. The diagnosis of hemophilia was complicated with several other issues that had the capacity of greatly diminishing their quality of life at he same time lowering the life expectancies never-mind the hemophilia.
Children born from the mid 90s to present have seen a new horizon. The treatments for this group of hemophiliacs has become safe by all estimations, free of disease and corrects the bleeding problem quickly. Other than having infusions of IV push (which they can do in their own home in about 15-20 minutes) these individuals would not have any identifier as being different from anyone else. Their quality of life still depends on many factors, but hemophilia is not one of the major players.
Still curious? Ask our experts.
Chat with our AI personalities
Blake
Ezra
Judy
Add your answer:
Earn +20 pts
How many people get hemophilia a year?
You have to be born with hemophilia, it is not something people can "catch".
What is the life expectancy of people with hemophilia?
The life expectancy of individuals with hemophilia has significantly improved over the years with advancements in medical care. With appropriate treatment and management, people with hemophilia can have a near-normal life expectancy. However, life expectancy may still be slightly reduced compared to the general population due to the risk of complications from bleeding episodes.
How long is a life span if you have hemophilia?
About 41
Can you develop hemophilia later in life?
Yes, it is possible to develop hemophilia later in life, although it is rare. Acquired hemophilia can occur in adults due to certain medical conditions or medications that interfere with the body's ability to clot blood.
Explain why hemophilia is a serious disorder?
Hemophilia is a serious disorder because it impairs the blood's ability to clot properly, leading to excessive bleeding from even minor injuries. This can result in internal bleeding, joint damage, and life-threatening bleeding episodes. Without proper management and treatment, hemophilia can greatly impact a person's quality of life and lead to serious complications.
When does hemophilia occurs?
Hemophilia is a genetic disorder that is present from birth. It is caused by mutations in the genes responsible for producing clotting factors, leading to difficulties in blood clotting and excessive bleeding. Symptoms can appear early in childhood but sometimes may not be apparent until later in life.
Can people with hemophilia live on their own?
Yes of course, people with hemophilia live with it there whole lives so they learn to be very cautious.
What kinds of people have more of a chance of getting hemophilia?
Hemophilia is an X-linked genetic disorder, so it is more common in males. People with a family history of hemophilia are also at a greater risk of inheriting the disorder.
What is an inherited abnormality that causes a deficiency of a specific clotting factor resulting in a reduced ablitity to clot blood?
Hemophilia is a bleeding disorder that slows down the blood clotting process. People who have hemophilia often have longer bleeding after an injury or surgery. People who have severe hemophilia have spontaneous bleeding into the joints and muscles. Hemophilia occurs more commonly in males than in females.The two most common types of hemophilia are hemophilia A (also known as classic hemophilia) and hemophilia B (also known as Christmas disease). People who have hemophilia A have low levels of a blood clotting factor called factor eight (FVIII). People who have hemophilia B have low levels of factor nine (FIX).The two types of hemophilia are caused by permanent gene changes (mutations) in different genes.
What percent of peoplehave hemophilia?
Hemophilia affects approximately 1 in 10,000 people. The percentage is then approximately 0.01%.
Are people with Hemophilia prevented of getting Malaria?
No, hemophilia does not confer an advantage against malaria. People with sickle-cell anemia do have an immunity, of sorts.
What is the age range for hemophilia?
People with hemophilia usually live until they bleed nonstop. Sure if they are in a car accident and have a major artery severed. These days adult hemophiliacs are dealing with issues that most elderly people do. Liver disease is probably the deadliest part of having hemophilia if you received blood product in the 80's. Aside from that, we manage our bleeding disorder and live long prosperous lives. Stepping in front of buses and riding a motorcycles without a helmet are just as stupid for us to do as anyone else.
