Sickle Cell Anemia Treatment in India

Sickle Cell Anemia (SCA) is a genetic blood disorder in which red blood cells become crescent-shaped, leading to chronic anemia, pain crises, organ damage, and increased infection risk. Early diagnosis and comprehensive management can significantly improve quality of life and reduce complications.

India offers advanced hematology care, specialized centers for blood disorders, and genetic counseling for SCA patients.

Symptoms of Sickle Cell Anemia

  • Chronic fatigue and weakness

  • Episodes of severe pain (pain crises)

  • Swelling in hands and feet

  • Frequent infections

  • Delayed growth or puberty

  • Vision problems and organ complications

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Treatment Options

Curative / Long-term Management

  • Bone Marrow / Stem Cell Transplant: Only potential cure; usually for children or young adults

  • Gene Therapy (Experimental): Advanced centers offer gene-editing options in select cases

Supportive / Symptomatic Care

  • Hydroxyurea Therapy: Reduces frequency of pain crises and need for transfusions

  • Blood Transfusions: Manage severe anemia or prevent stroke

  • Pain Management: Analgesics during pain crises

  • Antibiotics and Vaccinations: Prevent infections

  • Folic Acid Supplementation: Supports red blood cell production


Sickle Cell Anemia Treatment Cost in India

Table 1: Average Sickle Cell Anemia Treatment Cost in India

Type of TreatmentMinimum Cost (INR)Maximum Cost (INR)Approx. USD Range
Bone Marrow / Stem Cell Transplant₹15,00,000₹35,00,000$18,050 – $42,150
Hydroxyurea Therapy (per month)₹5,000₹15,000$60 – $180
Blood Transfusions (per session)₹15,000₹50,000$180 – $600
Supportive Care & Medications₹1,00,000₹3,00,000$1,200 – $3,610
Genetic Counseling & Testing₹10,000₹30,000$120 – $360

Factors Affecting Cost

  1. Type of treatment – Transplant, gene therapy, or supportive care

  2. Frequency of hospital visits – Regular transfusions or outpatient therapy

  3. Hospital facilities – Advanced hematology centers may charge more

  4. Patient complications – Organ damage or infection may increase cost

  5. Follow-up care – Medications, blood tests, and monitoring


Who Should Get Sickle Cell Anemia Treatment?

  • Children and adults diagnosed with SCA

  • Patients with frequent pain crises or severe anemia

  • Individuals with organ complications or stroke risk

  • Families seeking genetic counseling for SCA

  • Patients referred by hematologists or pediatric specialists


Benefits of Timely Treatment

  • Reduces frequency and severity of pain crises

  • Prevents complications such as stroke, organ damage, and infections

  • Improves quality of life and longevity

  • Bone marrow transplant offers potential cure in select cases

  • Ongoing supportive care ensures better long-term management

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With a focus on patient safety, precision, and compassionate care, our doctors ensure that every patient receives the highest standard of treatment. From initial consultation to recovery and follow-up, you are supported by a dedicated team of specialists, nurses, and coordinators who are committed to your well-being.

Comprehensive Range of Services Under One Roof

At Avicenna Global, we make your healthcare journey smooth and stress-free by bringing together a complete spectrum of medical and support services in one place. From initial consultation and diagnosis to advanced treatment, recovery, and post-care follow-ups, everything is managed seamlessly for you

Commitment to Safety, Quality, and Innovation

At Avicenna Global, we place patient safety and quality of care at the heart of everything we do. Partnering with internationally accredited hospitals (JCI & NABH) and certified specialists, we ensure that every treatment is delivered with the highest standards of medical excellence.

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