Aplastic Anaemia: When the Bone Marrow Stops Working
When Blood Production Fails
Aplastic anaemia is a life-threatening condition where the bone marrow stops making enough red blood cells, white blood cells, and platelets — leading to anaemia, infections, and uncontrolled bleeding simultaneously.
Causes in the Nigerian Context
- Autoimmune — in most cases, the immune system attacks stem cells in the bone marrow
- Medications and chemicals — chloramphenicol (widely used in Nigeria) is a notorious drug cause. Benzene exposure (from petroleum products) is also recognised
- Viral infections — hepatitis B, hepatitis C, and HIV (all highly prevalent in Nigeria) can trigger aplastic anaemia
Recognising the Symptoms
- Fatigue and breathlessness (from anaemia)
- Frequent or severe infections (from low white cell count)
- Easy bruising, prolonged bleeding, nosebleeds (from low platelets)
- Fever without obvious infection
Treatment and Support
Aplastic anaemia requires haematologist management: immunosuppressive therapy or bone marrow transplant for severe cases. Early referral to a tertiary centre with haematology services is essential. FXMed can support investigation of the underlying cause (viral serology, medication review, toxin exposure assessment) and nutritional support during recovery.
Ready to Take Action?
FXMed's Immune Support Programme is designed for busy Nigerians who want real answers — not generic advice.
About the Author
FXMed Team
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