- How does thalassemia minor affect the body?
- Can I take iron if I have thalassemia minor?
- Can minor thalassemia drink alcohol?
- Is thalassemia minor contagious?
- How do you know if you have thalassemia minor?
- What should I do if I have thalassemia minor?
- Can a thalassemia minor donate blood?
- Should I marry a thalassemia minor girl?
- What should be avoided in thalassemia minor?
- Does thalassemia minor affect fertility?
- Can thalassemia minor be cured?
- Is thalassemia minor normal?
- What should a thalassemia minor eat?
- Does exercise help thalassemia?
- Does thalassemia affect the liver?
- How do you treat thalassemia minor naturally?
- Is thalassemia minor a disability?
- How long do thalassemia patients live?
How does thalassemia minor affect the body?
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..
Can I take iron if I have thalassemia minor?
Thalassemia trait will not impair your work, diet or exercise. Trait carriers should not take iron supplements unless a special blood test (serum iron or serum ferritin) shows that you are iron deficient. Carriers can give blood providing they are not anemic (do not have a lower hemoglobin than usual).
Can minor thalassemia drink alcohol?
Patients with thalassaemia should be discouraged from consuming alcohol, as it can facilitate the oxidative damage of iron and aggravates the effect of HBV and HCV on liver tissue.
Is thalassemia minor contagious?
People who are carriers of a thalassemia gene show no thalassemia symptoms and might not know they’re carriers. If both parents are carriers, they can pass the disease to their kids. Thalassemias are not contagious.
How do you know if you have thalassemia minor?
People who have thalassemia trait (also called thalassemia minor) carry the genetic trait for thalassemia but do not usually experience any health problems except perhaps a mild anemia. A person may have either alpha thalassemia trait or beta thalassemia trait, depending upon which form of beta protein is lacking.
What should I do if I have thalassemia minor?
People with thalassemia minor or trait usually do not need blood transfusions because they either do not have anemia or have only a mild anemia. Many times people with thalassemia are prescribed a supplemental B vitamin, known as folic acid, to help treat anemia. Folic acid can help red blood cells develop.
Can a thalassemia minor donate blood?
A:An anaemic patient should defer blood donation till he is asymptomatic. An individual with thalassaemia trait having a haemoglobin value of more than 12.0 g/dl can donate blood, as can all other healthy family members.
Should I marry a thalassemia minor girl?
Can she conceive? A:A person, who is going to marry thalassemia minor, should check his/her thalassemia status before marriage to avoid the birth of thalassemia major. If both are thalassemia minor, there is 25% chances of thalassemia major in offspring, 25% chances of normal offspring and 50% chances of minor.
What should be avoided in thalassemia minor?
Thalassemia patients should avoid pork, liver, oysters, beans, beef, peanut butter and tofu from their diet. They should also avoid consumption of prunes and prune juice, watermelon, spinach, leafy green veggies, dates, broccoli, raisins and peas.
Does thalassemia minor affect fertility?
Barriers to fertility in women and men with thalassemia The iron overload associated with thalassemia can affect the development of both male and female sex organs, which can in turn affect the reproductive capabilities of a person with thalassemia. A person with thalassemia may experience delayed puberty.
Can thalassemia minor be cured?
Blood transfusions and chelation do not cure beta thalassemia. A stem cell transplant can cure it, but it is a serious procedure with many risks and won’t benefit everyone with the condition. Doctors and scientist are working on developing gene therapies and other treatments to help people with beta thalassemia.
Is thalassemia minor normal?
Persons with thalassemia minor have (at most) mild anemia (slight lowering of the hemoglobin level in the blood). This situation can very closely resemble that with mild iron-deficiency anemia. However, persons with thalassemia minor have a normal blood iron level (unless they are iron deficient for other reasons).
What should a thalassemia minor eat?
Nutrition & 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.
Does exercise help thalassemia?
Exercise is part of an overall healthy lifestyle and helps lead to better health outcomes. Although some people with thalassemia may have trouble participating in vigorous forms of exercise, many people with thalassemia can participate in moderate physical activities including biking, running, and walking.
Does thalassemia affect the liver?
Current HBsAg positivity in thalassaemia major ranges from <1% to >20% and Hepatitis B infection remains a significant cause of chronic liver disease and hepatocellular carcinoma in patients with thalassaemia in many regions of the developing world.
How do you treat thalassemia minor naturally?
You can help manage your thalassemia by following your treatment plan and adopting healthy-living habits.Avoid excess iron. Unless your doctor recommends it, don’t take vitamins or other supplements that contain iron.Eat a healthy diet. Healthy eating can help you feel better and boost your energy. … Avoid infections.
Is thalassemia minor a disability?
The RPWD Act 2016 has recognised persons with blood disorders (Thalassemia, Hemophilia and Sickle Cell Disease) as ‘persons with disabilities’ under the Act. Those with 40% and above disability will be given a Disability Certificate.
How long do thalassemia patients live?
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.