THALASSEMIA

What is Thalassaemia? — Understanding the Blood Disorder and How You Can Help

Thalassaemia is a genetic blood disorder that stops the body from producing enough hemoglobin, the protein in red blood cells that carries oxygen throughout the body. Without enough hemoglobin, organs and tissues do not get the oxygen they need, which can lead to severe anemia, fatigue, and serious health problems.

Children with thalassaemia often need regular blood transfusions throughout their lives to survive. Along with transfusions, they also require treatment to remove excess iron that builds up from repeated blood transfusions.

Types of Thalassaemia

Thalassaemia comes in two main types: Alpha Thalassaemia and Beta Thalassaemia. Each type affects the body differently and requires careful care.

Alpha Thalassaemia

Alpha thalassaemia happens when the body produces too few alpha globin chains.

Hemoglobin H Disease: Causes anemia and red blood cell destruction.
Hemoglobin H-Constant Spring Disease: A more severe form with significant red blood cell breakdown.
Alpha Thalassaemia Major: The most serious type, where the fetus produces no alpha globins and cannot survive without intervention.

Early diagnosis is essential, especially for expecting mothers, to manage risks and provide proper care.

Beta Thalassaemia

Beta thalassaemia is common in Pakistan, affecting about 6% of the population. In this type, red blood cells are fragile and cannot make enough healthy hemoglobin.

Symptoms of Beta Thalassaemia Major include
Pale skin and fatigue
Poor appetite and irritability
Delayed growth
Enlarged spleen or liver

Without regular treatment, patients cannot survive. Blood transfusions are required every month, sometimes even more often. Over time, repeated transfusions cause iron buildup in the body, which is treated using iron chelation therapy.

How Thalassaemia is Treated

While there is no simple cure, several treatments help patients lead healthier lives:

Blood Transfusions: Provide the red blood cells patients need to stay healthy.
Iron Chelation Therapy: Removes excess iron caused by repeated transfusions.
Splenectomy (Removal of the Spleen): Reduces red blood cell destruction in certain cases.
Bone Marrow or Stem Cell Transplant: Can be a life-saving solution for some patients if a compatible donor is available.

Regular care, proper nutrition, and medical supervision are essential to help patients live longer and healthier lives.

Living with Thalassaemia

Thalassaemia patients not only need medical treatment but also emotional support. Families, doctors, and organizations like Alizaib Foundation play a vital role in helping patients cope with the daily challenges of this condition. Every donation and act of support directly impacts these lives, providing the treatment, care, and hope that patients desperately need.

Prevention and Awareness

While thalassaemia is an inherited condition, taking preventive steps can save countless lives. Premarital and prenatal genetic screening can help identify carriers, and educating families about managing and preventing the disease ensures better outcomes. Community awareness campaigns encourage voluntary blood donation and support for patients, creating a stronger network of care throughout the country.

How You Can Help

You can make a real difference today. Every blood donation can be life-saving for a child with thalassaemia, sponsoring a patient helps cover the cost of transfusions and treatment, and volunteering or spreading awareness inspires others to take action. At Alizaib Foundation, your contribution ensures that every patient receives free, safe, and timely care. Together, we can restore health, give hope, and build a thalassaemia-free Pakistan. Join our mission today and save a life.

We are a non-profit organization committed to building a healthier, thalassaemia-free Pakistan. Through continuous blood donation drives, patient support programs, and nationwide awareness campaigns, we work every day to save lives and spread hope. Together, we can ensure that no child suffers because of thalassaemia.

 
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