MBBS, MD, DM (Clinical Haematology)
Principal Director & Chief Hematology at Fortis Hospital
Principal Director & Chief Hematology at Fortis Hospital
MBBS, MD, DM (Clinical Haematology)
$12,000–24,000 USD for a matched sibling donor; higher for unrelated donors.
Yes, many private insurers and government schemes offer partial or full coverage.
Yes, through a successful bone marrow transplant in suitable candidates.
Typically every 2 to 4 weeks.
Absolutely. With experts like Dr. Bhargava and modern hospital facilities, outcomes are excellent.
Thalassemia is a genetic blood disorder that affects the production of healthy hemoglobin and red blood cells. Managing this condition often involves long-term treatment, with some cases requiring advanced procedures like bone marrow transplants. In India, treatment costs can vary based on the chosen approach —ranging from $12–36 USD per blood transfusion to $12,000–24,000 USD for a bone marrow transplant. This guide outlines the treatment options, their associated costs, and why many patients place their trust in Dr. Rahul Bhargava, one of India’s most experienced hematologists.
Thalassemia is a hereditary blood disorder that affects the body’s ability to produce enough healthy hemoglobin—the protein in red blood cells responsible for carrying oxygen. As a result, individuals with thalassemia experience chronic anemia, which can lead to fatigue, weakness, and complications affecting various organs if not managed properly.
This condition is caused by mutations in the genes responsible for hemoglobin production and is usually inherited from both parents. The severity of thalassemia depends on the type and number of genetic mutations involved.
There are three main types:
This is the most severe and life-threatening form of thalassemia. It usually becomes apparent within the first two years of a child’s life. Individuals with thalassemia major require regular blood transfusions—sometimes as often as every two to four weeks—to maintain healthy hemoglobin levels. Without treatment, it can lead to severe anemia, growth delays, bone deformities, and organ complications.
A less severe form of the disease, thalassemia intermedia presents with milder symptoms that may not appear until later in childhood or adolescence. Patients might require occasional blood transfusions, particularly during periods of stress, illness, or surgery. Regular monitoring and supportive therapies like iron chelation are often part of the care plan.
This is the mildest form and usually does not cause any health issues. Most people with thalassemia minor are carriers of the genetic trait and do not require treatment. However, they can pass the gene to their children. It’s important for carriers to undergo genetic counseling, especially when planning to start a family.
Understanding the type and severity of thalassemia is essential for planning the appropriate course of treatment and long-term management. Early diagnosis, made possible through genetic testing and regular screening, allows for timely medical intervention and significantly better outcomes. for planning the appropriate course of treatment. Early diagnosis, made possible through genetic testing and blood work, allows for timely intervention and a better quality of life.
Treating thalassemia involves ongoing medical care and, in some cases, curative treatment. Below are the main approaches and their typical costs in India.
This is the foundation of treatment for patients with thalassemia major.
Frequent transfusions can lead to iron buildup in the body, which can damage organs. Iron chelation helps remove this excess iron.
Chelation is essential to avoid complications like liver and heart damage.
A bone marrow transplant is currently the only known cure for thalassemia.
The success rate improves with early intervention, especially in younger children without other health complications.
In addition to treatment, patients may also need to cover:
Dr. Rahul Bhargava, Head of Hematology and Bone Marrow Transplant at Fortis Memorial Research Institute, Gurugram, is one of India’s leading experts in thalassemia treatment.
Patients under Dr. Bhargava’s care receive individualized plans, access to cutting-edge therapies, and compassionate support through every step of the journey.
The long-term outlook for thalassemia patients has improved significantly over the past decade, especially with advances in diagnosis, treatment, and supportive care. Many individuals with thalassemia can live active, fulfilling lives when the condition is properly managed.
Other factors that influence outcomes include the patient’s age, overall health, iron levels, and the presence of any complications. With continuous improvements in transplant techniques, supportive care, and medications, the survival and cure rates are higher than ever.
India has emerged as a global hub for affordable, high-quality thalassemia treatment. Every year, hundreds of patients from countries like the UAE, Iraq, Nigeria, Bangladesh, and Nepal travel to India to receive specialized care.
Key reasons why international patients prefer India include:
Living with thalassemia presents challenges, but with the right medical care, it’s manageable—and even curable. India offers one of the most cost-effective and comprehensive care options globally, with expert specialists like Dr. Rahul Bhargava leading the way.
Whether you’re seeking routine care or a curative transplant, Dr. Bhargava and his team at Fortis Memorial Research Institute, Gurugram, provide world-class support every step of the way.
To book a consultation or get a tailored treatment estimate, contact Dr. Rahul Bhargava today.