Question: How Long Do Thalassemia Patients Live?

How does thalassemia affect your life?

Thalassemia (thal-uh-SEE-me-uh) is an inherited blood disorder that causes your body to have less hemoglobin than normal.

Hemoglobin enables red blood cells to carry oxygen.

Thalassemia can cause anemia, leaving you fatigued.

If you have mild thalassemia, you might not need treatment..

Does thalassemia affect immune system?

Because of this, people with thalassemia are said to be “immunocompromised,” which means that some of the body’s defenses against infection aren’t working. When you are immunocompromised, it is easier for you to get infections and you sometimes need extra protection, like flu shots and other vaccines.

Can thalassemia minor get married?

If anyone is a carrier and gets married to a person with normal genotype, there is a 50% chance / possibility of having an offspring with thalassaemia carrier status. However, no thalassaemia major birth (baby with thalassaemia) would happen.

Can thalassemia drink coffee?

Coffee, tea and spices like oregano can decrease absorption of iron. Thalassemia patients can have tea and coffee in abundance. Milk, cheese, yogurt and other dairy products can decrease absorption of iron the body.

Is thalassemia considered a disability?

Only those with fairly low income and assets are eligible for SSI, even if they meet the medical eligibility criteria. With regard to medical eligibility, the SSA considers beta thalassemia an inherently disabling disease.

Is thalassemia sexually transmitted?

Blood-borne pathogens or a drop in blood supply could potentially affect a thalassemia patient. HIV (Human Immuno-deficiency Virus) is a blood-borne pathogen and a sexually-transmitted disease. From 1978 to 1985, there was a peak in contamination of the blood supply with HIV.

What is the best treatment for thalassemia?

Standard TreatmentsBlood Transfusions. Transfusions of red blood cells are the main treatment for people who have moderate or severe thalassemias. … Iron Chelation Therapy. The hemoglobin in red blood cells is an iron-rich protein. … Folic Acid Supplements. … Blood and Marrow Stem Cell Transplant. … Possible Future Treatments.

How long is the life of thalassemia patients?

A person with the thalassemia trait has a normal life expectancy. However, heart complications arising from beta thalassemia major can make this condition fatal before the age of 30 years.

Can thalassemia be cured?

A stem cell transplant is the only treatment that can cure thalassemia. But only a small number of people who have severe thalassemias are able to find a good donor match and have the risky procedure. For more information, go to the Health Topics Blood and Marrow Stem Cell Transplant article.

Is thalassemia a serious disease?

Alpha Thalassemia Major is a very serious disease in which severe anemia begins even before birth. Pregnant women carrying affected fetuses are themselves at risk for serious pregnancy and delivery complications. Another type of Alpha Thalassemia is Hemoglobin H disease.

What should we eat in thalassemia?

Nutrition & Thalassemia Nutritional deficiencies are common in thalassemia. It is recommended that patients going through blood transfusion should opt for a low iron diet. Avoiding iron-fortified foods like cereal, red meat, green leafy vegetables & Vitamin C-rich foods is the best option for thalassemic patients.

Is milk good for thalassemia?

Calcium. Many factors in thalassaemia promote calcium depletion. A diet containing adequate calcium (e.g. milk, cheese, dairy products and kale) is always recommended.