Thalassemia in Bangladesh: Awareness, Prevention & Care
Thalassemia is one of the most significant yet preventable public health challenges in Bangladesh. Classified as a hereditary blood disorder, it affects the body’s ability to produce healthy hemoglobin, leading to chronic anemia and life-threatening complications if left unmanaged.
Prevent Thalassemia: Protect Your Future Family
A preventable genetic disorder. One simple test can make a lifelong difference.
What is Thalassemia?
Thalassemia is a hereditary blood disorder common in Bangladesh. It prevents the body from making enough healthy hemoglobin.
- The Carrier: Looks and feels healthy, but carries the gene.
- The Patient: Suffers from severe anemia, requiring lifelong blood transfusions.
The Reality in Bangladesh
- 1 in 10 people in Bangladesh is a carrier.
- 7,000+ children are born with the disease every year.
- 100% of these cases could have been prevented with a simple blood test.
Are You a Carrier?
Most carriers have no symptoms. You won’t know unless you test
If both partners are carriers, for each pregnancy there is:
- 25% chance of an affected child
- 50% chance of a carrier child
- 25% chance of a non-carrier child
Early identification allows couples to seek appropriate medical guidance.
Who Should Get Tested?
1.Before Marriage: Every young adult should know their status.
2.Planning a Family: Couples who haven’t been screened.
3.Family History: If a relative has Thalassemia or is a carrier.
The “Safe Marriage” Rule
- Carrier + Non-Carrier:
- Non-Carrier + Non-Carrier:
- Carrier + Carrier: High Risk. Seek Genetic Counseling immediately.
Our Diagnostic Services
We provide high-precision screening to give you peace of mind.
- Complete Blood Count (CBC): Initial screening for anemia markers.
- Hb Electrophoresis: The gold standard test to confirm carrier status.
- Expert Counseling: Guidance on how to interpret your results.
Contact us today to book your screening and secure the health of your future generations.
