

Tackling sickle cell and hepatitis in Nigeria
Media firm celebrates Sickle cell people

Genotype testing helps avoid genetic diseases in children, says expert



NGOs raise alarm over rising sickle cell cases


Sickle Cell: 250 million people affected globally, says Nigerian Orthopaedic Association




Sickle Cell: NBA to sponsor mandatory Genotype Bill in Ekiti


20 per cent of Nigerian children living with sickle cell — NDHS Report


People living with Sickle Cell need empathy, not sympathy — Obasanjo

Sickle cell: Association presents Bill to Kebbi House of Assembly

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Sickle Cell: Medical centre performs Stem Cell transplant for two
By Gabriel Enogholase – Benin A Benin based Medical Hospital, CELLTEK HEALTH MEDICAL CENTRE, has successfully performed the stem cell transplant of two sickle cell children ages 4 and 6 years by using their mothers’ (hyplo transplant) that are half matched with their hemoglobin. Medical Director of the centre, Prof. Godwin Bazuaye who disclosed this […]

Avoid self-pity, consultant tells sickle cell patients
At a time when over 40% of youths are unemployed, getting gainful employment for youths with disabilities becomes much more difficult.

Avoid self-pity, consultant tells sickle cell patients
At a time when over 40% of youths are unemployed, getting gainful employment for youths with disabilities becomes much more difficult.

The debt the black race owes the sickle cell disease patient
As we celebrate this year’s World Sickle Cell Day, Nigerians need to take a pause and appreciate what the disease means to us as nation, in particular and to the Black race, in general. I wonder how many Nigerians are aware that the country is the epicenter of the disease worldwide with the highest prevalence figures. While there are about 300,000 babies born with the disease in the world every year, about half of these are born in Nigeria! Indeed, it is estimated that 2% of all Nigerian newborns are affected by the disease, and about 30% carry the trait.

Sickle Cell: NGO advocates premarital screening
The Sickle Cell Hope Alive Foundation (SCHAF) says voluntary premarital genetic screening remains key to reducing the high incidence of Sickle Cell Disease (SCD) in Nigeria.

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