Your Blood Health, Our Expertise
08:30-16:00
This is an overview of the services we provide to you
Diagnosis and treatment of anaemias, clotting disorders, and platelet abnormalities.
Specialised care for leukaemias, lymphomas, myelomas, and other haematologic malignancies.
We coordinate and manage bone marrow transplants with pre- and post-transplant support.
Diagnosis and management of inherited and acquired immune system disorders.
Safe, evidence-based transfusion services tailored to each patient’s needs.
Efficient treatment for iron-deficiency anaemia under monitored clinical conditions.
Conditions include anemia (especially iron deficiency), hemophilia, von Willebrand disease, platelet disorders, autoimmune hemolytic anemias, thrombocytopenia, sickle cell disease, hemoglobinopathies, and others
Chemo, radiation, targeted therapy, immunotherapy, and sometimes stem cell transplant.
When oral iron is ineffective or there’s intolerance. It’s used in cases like confirmed iron-deficiency anemia where rapid restoration is desired.
Small risks include allergic reactions or anaphylaxis, and possible skin pigmentation changes at infusion sites
Symptoms vary by disorder but may include fatigue, shortness of breath (red cell issues), fever/infections (white cell issues), easy bruising, heavy bleeding, or skin rash (platelet/clotting issues)
HSCT replaces diseased or damaged blood-forming stem cells, most often destroyed by chemotherapy or radiation with healthy ones from the patient’s body (autologous) or a donor (allogeneic)
After harvesting, conditioning (chemo/radiation) kills diseased marrow, followed by infusion of stem cells; engraftment (new blood cell production) usually begins around 12–15 days post-transplant
Donated blood is screened for infections (HIV, hepatitis, syphilis), typed for ABO and Rh, and sometimes CMV, especially for immunocompromised recipients. Leukodepletion is commonly used to reduce CMV risk