“I can love just like you,
I can dance just like you,
I can run just like you,
and more importantly – I can work just like you.
Yet, all I wish is if I could make red blood – just like you.”

Partth Thakur

“I can love just like you, I can dance just like you, I can run just like you and more importantly, I can work just like you. Yet, all I wish is if I could make red blood - just like you.”

Curious about Thalassemia? Discover essential insights!

  • Thalassemia is an inherited condition, passed from parents to children, just like other physical characteristics such as eye color or nose shape.
  • Thalassemia cannot be acquired or caught through other means.
  • Some individuals are healthy “carriers” of thalassemia, often unaware of their status.
  • When both parents are carriers, there is a 25% chance that their baby will be born with thalassemia in every pregnancy.
  • Such couples are referred to as a “couple at risk” due to the 25% risk of the baby being born with thalassemia each time they have a child.
Thalassemia is a condition which affects the production of red blood cells. Children who are born with Thalassemia cannot make enough healthy red blood cells, so without medical treatment most would get weaker and would fail to develop and grow normally. People with thalassaemia major will need special medical care throughout their lives. The main treatments are :

Blood Transfusions – regular blood transfusions treat and prevent anaemia; in most cases these are needed around twice a month.

Chelation Therapy – treatment with medicine to remove the excess iron from the body that builds up as a result of having regular blood transfusions.
Thalassemia is a condition which affects the production of red blood cells. Children who are born with Thalassemia cannot make enough healthy red blood cells, so without medical treatment most would get weaker and would fail to develop and grow normally. People with thalassaemia major will need special medical care throughout their lives. The main treatments are :

Blood Transfusions – regular blood transfusions treat and prevent anaemia; in most cases these are needed around twice a month.

Chelation Therapy – treatment with medicine to remove the excess iron from the body that builds up as a result of having regular blood transfusions.

Thalassemia is a Preventable Disaster.

Thalassemia is not just a long medical word. It’s a serious inherited blood disorder in which the body fails to produce enough healthy red blood cells. For someone born with Thalassemia Major, this means they need regular blood transfusions to survive, often every two to three weeks, starting from early childhood.

But blood alone isn’t enough.

Those frequent transfusions cause excess iron to build up in the body, which can damage the heart, liver, and other organs. That’s why patients also need daily medication called chelation therapy to remove the excess iron and keep their bodies safe.

Now here’s the tougher part: while all of this sounds routine on paper, it’s not so easy in real life. Access to safe blood, reliable chelation medicines, trained specialists, and regular monitoring is a challenge for many families, especially those from lower-income backgrounds. And unfortunately, without consistent care, complications pile up quickly.

Thalassemia is manageable and even curable in some* cases; when there is proper awareness, timely support, and access to care. That’s what we’re here to fight for.

So What Does Treatment Really Look Like?

Treating Thalassemia is not a one-time thing. It’s a lifelong journey, and it’s different for every warrior.

It usually involves:

  1. Regular Blood Transfusions: Most Thalassemia Major patients need transfusions every 2 to 3 weeks. These help maintain healthy hemoglobin levels and give the body the energy it needs. But it also means constant visits to hospitals and a steady supply of safe, screened blood, which isn’t always guaranteed, especially in smaller towns.
  1. Chelation Therapy: Too many transfusions can cause excess iron to build up in the body. That’s where chelation therapy steps in. It’s a daily medication that helps remove this extra iron, protecting the heart, liver, and other organs. Skipping chelation? Not an option — but sadly, many families can’t afford it or don’t even know how vital it is.
  1. Monitoring & Specialist Care: Thalassemia affects more than just blood. It can impact growth, immunity, bones, and even mental health. That’s why regular tests, doctor consultations, and hormone monitoring are so important — especially during teenage years and early adulthood.
  2. Bone Marrow Transplant (BMT): This is currently the only known cure for Thalassemia. A successful BMT replaces the faulty blood-making system with healthy stem cells from a matching donor. However, the procedure is expensive, not always accessible, and requires finding a suitable match, which is not always easy.
At The Wishing Factory, we work to make this whole journey less lonely and more supported — by raising awareness, providing treatment support, and simply being there through it all.

Know About #TheThalaTest

The Thala Test is a simple blood test that checks whether a person is a carrier of Thalassemia. Being a carrier does not mean you are sick or will ever need treatment. Most carriers live completely normal lives and often never know they carry the gene unless they get tested.

But here’s the important part: if both partners are carriers, there is a high chance that their child could be born with Thalassemia Major, a lifelong condition that requires regular blood transfusions and constant medical care. One small test, done at the right time, can prevent a lifetime of struggle for a child.
When should it be done?
Ideally, the Thala Test should be done before marriage or before planning a family. This is when the information is most useful and empowering. It allows couples to make informed, responsible choices for their future, without panic or pressure.
Who should get tested?
The short answer: everyone.
Thalassemia does not belong to any one community, caste, religion, or income group. Anyone can be a carrier. That’s why we strongly believe that all individuals planning marriage or a family should get tested, regardless of background. Awareness should be universal, not selective.
What does the testing process look like?
The process is simple and straightforward. Both partners undergo a basic blood test called an HPLC test. It’s quick, affordable, and widely available.
If only one partner is a carrier, there is no risk of having a child with Thalassemia Major. If both partners are carriers, the next step is to consult a qualified doctor or genetic counsellor. They can guide the couple through safe and informed family planning options. Knowledge here does not limit choices, it opens them up.
Why we talk about the Thala Test so openly?
At The Wishing Factory, we’ve seen what life with Thalassemia looks like, not just in hospitals, but in homes, schools, and everyday routines. We believe prevention through awareness is one of the most powerful tools we have.
The Thala Test is not about fear. It’s about responsibility, compassion, and giving the next generation a healthier start. One test. One decision. A lifetime of impact.

The Thala Test is not about fear. It’s about responsibility, compassion, and giving the next generation a healthier start. One test. One decision. A lifetime of impact.

Help the warriors survive and get special medical care throughout their lives.

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