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Thalassemia मुक्त महाराष्ट्र

Since 2021, Wamanrao Oak Raktakendra has been working towards the mission - Thalassemia मुक्त महाराष्ट्र.

Thalassemia can be managed in three ways — CARE, CURE, and CURB. At WOBB, the major focus has been on the CURB approach, with the belief that prevention and awareness can protect future generations from genetic blood disorders like Thalassemia and Sickle Cell Disease.

The initiative primarily creates awareness among young individuals between 15 to 35 years of age about the importance of premarital testing and timely screening.

Through awareness drives, counselling sessions, and collaborations with gynaecologists, paediatricians, pathologists, WOBB continues to encourage responsible and informed healthcare decisions.

A major contribution to this mission has come from Dr. Ulhas Vaidya, whose support has been instrumental in strengthening the initiative. The testing and validation of more than 10,500 collected samples were successfully carried out at his pathology laboratory, providing a strong diagnostic foundation to the project.

With continuous community participation and healthcare collaboration, WOBB remains committed to building awareness and working steadily towards Thalassemia मुक्त महाराष्ट्र

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Join the movement & Spread awareness

What is Thalassemia and
Sickle Cell Anaemia

Thalassemia and Sickle Cell Disease are inherited blood disorders passed from parents to children. In Maharashtra, nearly 2 out of every 100 people may carry the Thalassemia trait, while around 6 out of every 100 may carry the Sickle Cell trait.

Many remain unaware of their carrier status, which increases the risk of children being born with Thalassemia Major. Early screening and awareness can help prevent these disorders in future generations.

Our Impact & Mission at a Glance

97
Thalassemia Awareness Camps
10500
Screening & Testings
400
Thalassemia Minor Detections
200
Sickle Cell Carriers Identified

How can you Help

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Get Screened Early

Take a simple Thalassemia and Sickle Cell screening test and know your carrier status.

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Stop the Stigma

Encourage open conversations around premarital screening and help remove the fear and social stigma associated with genetic testing.

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Spread Awareness

Educate family, friends, and communities about prevention, early detection, and informed healthcare decisions. Participate in awareness camps, community initiatives, and screening programs to help build a Thalassemia-Free Maharashtra.

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Donate Blood Regularly

Children with Thalassemia Major often require blood every 3–4 weeks to survive. Your blood donation can give them hope and a healthier life.

Frequently Asked Questions (FAQs)

Thalassemia Major is a serious condition where a child requires regular blood transfusions throughout life. Thalassemia Minor and Thalassemia Trait are generally the same — the person is a carrier and usually healthy, but can pass the gene to their children.

Yes. Both terms refer to a person who carries the Thalassemia gene but usually does not suffer from major health problems. However, screening is important before marriage and pregnancy.

Common early signs may include weakness, pale skin, tiredness, slow growth, low hemoglobin levels, and frequent fatigue. In many carriers, there may be no visible symptoms.

Yes. With proper medical guidance, genetic counseling, and timely prenatal testing, healthy pregnancy outcomes are possible even if both partners are carriers.

Early screening helps individuals know their carrier status and make informed healthcare decisions. Awareness and timely testing can help prevent future generations from being affected by Thalassemia Major.
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