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Thalassemia treatment in Turkey has shown notable success over the years. The condition, commonly known as Mediterranean anemia, is a genetic blood disorder affecting hemoglobin production in red blood cells, crucial for oxygen transport in the body. There is no permanent cure for thalassemia; however, the approaches employed in Turkey contribute significantly to managing the disease and alleviating its symptoms, ultimately enhancing the patient's overall quality of life.
Why do people choose Turkey for thalassemia treatment?
Turkish clinics are trusted by both local residents and international patients for thalassemia treatment. The high prevalence of thalassemia cases in Turkey contributes to the success of treatments provided by these clinics.
Thalassemia is widespread in Turkey, leading to a significant number of cases. However, clinics in the country have effectively treated these cases, achieving notable success rates.
International patients opt for thalassemia treatment in Turkey for various reasons. These include cost-effectiveness, increased chances of finding a donor, top-notch medical care, easy access to renowned doctors, minimal waiting times, and more.
Given these benefits, choosing Turkey for thalassemia treatment is a logical decision. The treatment cost of thalassemia in Turkey is 50-60% lower than in other countries, while the success rate remains impressively high.
Thousands of thalassemia patients treated with bone marrow transplant in Turkey

Image credit: Metro Hospital
Bone marrow transplant is the sole cure for thalassemia worldwide. Numerous patients with thalassemia in Turkey have undergone successful treatment through this method.
A-Medical recommends and facilitates bone marrow transplants in JCI accredited clinics. This method has demonstrated remarkable success, benefiting thousands of thalassemia patients.
How bone marrow transplantation works for thalassemia
Blood cells form in the bone marrow from stem cells. Individuals with thalassemia generate insufficient functional red blood cells, leading to reduced oxygen intake by the body.
The primary and most effective remedy for thalassemia is a bone marrow transplant. Once the donor's bone marrow is introduced into your body, it triggers the production of healthier blood cells in your own marrow.
Despite being a beneficial treatment, bone marrow transplantation carries potential life-threatening complications and is typically reserved for individuals with severe illnesses.
In allogeneic transplantation, one replaces their own bone marrow stem cells with those from a donor. The donor is typically a close genetic match, like a sibling or parent, although it can also be an unfamiliar individual.
Effect of treatment and risks
The most effective treatment for thalassemia today is bone marrow transplantation, especially when performed in childhood, yielding the best results.
Success in treating thalassemia through bone marrow transplantation hinges on donor compatibility, with a survival rate ranging from 66% to 99% when the donor is a sibling.
Following bone marrow transplantation, individuals find relief from thalassemia symptoms, leading to an enhanced quality of life.
However, this treatment method carries risks, including:
- Drop in blood pressure
- Headache
- Nausea
- Pain
- Shortness of breath
- Chills
- Fever
Furthermore, bone marrow transplantation may lead to complications such as:
- Graft-versus-host disease, where donor cells attack the recipient's body
- Graft failure, when transplanted cells fail to produce new cells
- Bleeding in the lungs, brain, and other body parts
- Cataracts, causing clouding in the eye lens
- Damage to vital organs
- Early menopause
- Anemia, a deficiency in red blood cell production
- Infections
- Nausea, diarrhea, or vomiting
- Mucositis, inflammation, and soreness in the mouth, throat, and stomach
Who is a candidate for the procedure in Turkey?
Eligibility for thalassemia treatment in Turkey through bone marrow transplantation is assessed individually, based on several key medical and genetic factors. The most critical considerations include the patient’s age and the availability of an HLA-identical family donor. Early intervention significantly improves success rates, so undergoing the transplant before the development of complications such as liver enlargement, liver fibrosis, or iron overload is strongly recommended.
At A-Medical, we specialize in organizing and coordinating thalassemia treatment in Turkey, ensuring a smooth, transparent, and stress-free process for every patient.
To begin your thalassemia treatment journey with A-Medical:
- Step 1: Contact us and share your latest medical reports. Our team will forward them to an experienced Turkish hematologist for expert evaluation.
- Step 2: A compatible donor is typically a sibling or close family member.
- Step 3: If no suitable donor is found within the family, we will facilitate an application to the Turkey Donor Bank or the World Donor Registry to identify a match.
If you meet the eligibility criteria or would like more information about your options, contact A-Medical via WhatsApp for personalized guidance and professional support throughout the entire treatment process.
What happens if I don't have a donor?
If you require thalassemia treatment in Turkey but don’t have a matching donor, A-Medical will guide you through every step of the process to help find one. Our team collaborates directly with both the Turkish Donor Bank and the World Donor Registry to locate a compatible match as quickly as possible.
Here’s what to do if you don’t have a donor:
📞 Contact us on WhatsApp to speak with our medical coordination team.
📋 Share your recent medical reports that include information about your current condition, diagnosis, and any relevant lab results.
🏥 A-Medical will prepare and submit your donor application to official donor banks in Turkey on your behalf, ensuring that the process is handled efficiently and in compliance with all medical and ethical standards.
Even without a family donor, patients still have a strong chance of receiving successful thalassemia treatment in Turkey through A-Medical’s global donor network and expert guidance.
Thalassemia treatment cost in Turkey
Thalassemia treatment in Turkey costs $60,000, exclusively for patients with sibling or parental donors.
If you lack a donor for thalassemia treatment, you can seek assistance from A-Medical. We guide you in finding a suitable donor, ensuring a smooth process.
For those without a donor, the cost of thalassemia treatment with bone marrow transplantation in Turkey is $75,000. This covers the search for a suitable donor from TürkKök, Turkey's donor bank. In cases where a local match is unavailable, A-Medical reaches out to European and American donor banks. The treatment cost, with donors from these banks, is $85,000.
The thalassemia treatment package in Turkey through A-Medical includes hotel accommodation for 60-90 days after the surgery.
Best clinics for thalassemia treatment in turkey

Memorial Clinic

Memorial Clinic is one of the leading centers for thalassemia treatment in Turkey, offering advanced hematology and bone marrow transplantation services. The hospital’s Prof. Betül Tavil, a highly respected pediatric hematologist, is recognized for her extensive experience in treating thalassemia patients with modern transplant techniques. The clinic is also known for its JCI accreditation, world-class infrastructure, and strong focus on international patient care.
Medstar Antalya Clinic

Medstar Antalya Clinic provides comprehensive diagnostic and treatment programs for thalassemia patients, including bone marrow transplantation and post-transplant follow-up care. The clinic’s Assoc. Dr. Burak Deveci leads the hematology and oncology department, specializing in pediatric and adult thalassemia cases. With its modern facilities, experienced transplant team, and personalized approach, Medstar Antalya has become one of the most trusted centers for thalassemia treatment in Turkey.
A-Medical works closely with both Memorial Clinic and Medstar Antalya Clinic, helping patients access these top-performing hospitals quickly and efficiently. Through A-Medical, you can benefit from faster application responses, discounted treatment packages, and full logistical support throughout your thalassemia treatment journey in Turkey.




