Thalassemia-Pune

Prevention-ZERO Thalassemia

We at the Thalassemia Society are committed for Prevention and Awareness drives in and around Pune. We have set a goal to achieve ZERO Thalassemia birth of new Patients in Pune by the year 2020.

As a part of this, we are planning to cover all corporates and colleges. We have conducted major awareness campaign in Infosys, Wipro, Fiat, VW, to name a few- where we have collected more than 500 samples for screening and are in process of counselling affected people with Thalassemia Trait. We are in process of similar mass awareness campaign / screening for prevention in various communities to create awareness of the disease condition .

Mission Statement

The Thalassemia Society Pune Chapter was founded by patients, parents and friends affected by Thalassemia. The foundation provides hope, comfort and encouragement to those battling this disorder. At the heart of the organization is a strong desire to help improve the quality of life for all patients with Thalassemia. We volunteer our time to organize conferences, raise funds to educate the community, ensure patients and parents know the latest in care.The foundation maintains a strong relationship with the medical community that provides diagnosis, treatment and care.

Join Us

Make A Donation

Surendra @ +91-976-651-1371

Email Us

Important Contacts

Office Phone - +91-844-671-6162 (Open from 10am-2pm)

Blood Filters - Mrs. Naina Doshi +91-927-004-9248

Frequently Asked Questions

Disclamer: Thalassemia Society Pune Chapter is not a medical service. The following information is provided to answer questions we are frequently asked but should not be taken as medical advice. All concerns about your health should be discussed with a health professional.

What is thalassemia?
Thalassemia (say "thal-uh-SEE-mee-uh") is an inherited blood disorder that causes your body to make less hemoglobin or abnormal hemoglobin. Hemoglobin helps red blood cells spread oxygen through your body. Low levels of hemoglobin may cause anemia, an illness that makes you feel weak and tired. Severe anemia can damage organs and lead to death.

What are the types of thalassemia?
There are two main types: alpha and beta. Beta thalassemia is the most common.
Beta thalassemia
You need both alpha- and beta-globin to make hemoglobin. Beta thalassemia occurs when one or both of the two genes that make beta-globin don't work or only partly work as they should.
• If you have one damaged gene, you may have mild anemia and probably won't need treatment. This is called beta thalassemia minoror beta thalassemia trait. It happens when you get a normal gene from one parent and a thalassemia gene from the other.
• When both genes are damaged, it means you got a thalassemia gene from each parent. You may have moderate or severe anemia.
o If you have moderate anemia (beta thalassemia intermedia), you may need blood transfusions.
o People with severe anemia (called beta thalassemia major orCooley's anemia) need blood transfusions throughout life. Symptoms of anemia usually begin within a few months after birth.

Alpha thalassemia
This type occurs when one or more of the four alpha-globin genes that make hemoglobin are missing or damaged.
• If one gene is missing or damaged: Your red blood cells might be smaller than normal. You will have no symptoms and you will not need treatment. But you are a silent carrier. This means you don't have the disease but can pass the defective gene to your child.
• If two genes are missing or damaged: You will have very mild anemia that will typically not need treatment. This is called alpha thalassemia minor or alpha thalassemia trait.
• If three genes are missing: You will have mild to moderately severe anemia. This is sometimes called hemoglobin H disease. If it is severe, you may need blood transfusions.
• If all four genes are missing: This is called alpha thalassemia majoror hydrops fetalis. The fetus will be stillborn, or the child will die soon after birth.


What causes thalassemia?
A defect in one or more genes causes thalassemia.
If you, either parent, or any of your siblings have thalassemia or carry a gene for thalassemia and you're thinking about having a child, you may want to talk to a genetic counselor before you get pregnant. A genetic counselor can tell you how likely it is that your child will have the disease and how severe it might be.

How is thalassemia diagnosed?
Your doctor will do an exam and ask about your health history. Tests you may need include:
• A complete blood count (CBC).
• A gene test to see if you have the genes that cause thalassemia.
• An iron level test.
• A blood test that measures the amounts of different types of hemoglobin, to help find out which type of thalassemia you have.
If you learn that you have thalassemia, your family members should to talk to their doctors about testing.

How is it treated?
Treatment depends on how severe your condition is.
Most large medical centers have treatment centers for blood disorders. They are an excellent resource to help you and your family get the best care.
• Mild thalassemia, the most common form, does not need treatment.
• Moderate thalassemia may be treated with blood transfusions and folic acid supplements. Folic acid is a vitamin that your body needs to produce red blood cells.
• Severe thalassemia may be treated with:
o Blood transfusions.
o Folic acid.
o Medicines that are used for chemotherapy (they help your body to make normal hemoglobin).
If you have repeated blood transfusions, it's possible for your body to get too much iron. This can damage your organs, especially the liver. Make sure to avoid vitamins that contain iron, and don't take extra vitamin C, which can increase how much iron you absorb from food. If you have too much iron, your doctor may give you chelation therapy. This is a medicine that helps remove iron from your body.
Less common treatments for severe thalassemia include:
• A blood or bone marrow stem cell transplant.
• Surgery to remove the spleen.

Get a flu vaccine each year. Also talk to your doctor about getting a pneumococcal vaccine. These vaccines may protect you from severe infections, which can make anemia worse and cause severe illness in people with thalassemia.

Disclamer: Thalassemia Society Pune Chapter is not a medical service. The following information is provided to answer questions we are frequently asked but should not be taken as medical advice. All concerns about your health should be discussed with a health professional.

Upcomming Events

Stay Tuned for Upcoming Events!

For Patients & Parents

Yearly Blood test for thalassemia patients at 25 % charges at ruby hall clinic


World Thalassemia Day 2016 on 8th May Sunday

If you unable to find blood. Contact Jatin @ +91-9822592370

DEXA Scan free of cost for 12 yrs and above patient @ KEM Hospital Pune Contact Jatin @ +91-9822592370

Thalassemia patient with HCV can get free treatment Plus Free HCV viral load test and genotype test. Contact us for more details

Recent Updates

Thalassemia awarness & screening drive @ Infosys Pune

Thalassemia awarness drive with Ishanya Youth @Pune Read More

Thalassemia awarness drive @ Bhor Pune with Dr. Pendse

Frequently Asked Questions