Genotype awareness drive targets students at Trinity University

Genotype awareness drive targets students at Trinity University

 

 

Genotype

 

 

By correspondent

 

Lagos, Feb. 18, 2026. The Gail Sickle Initiative, in partnership with Trinity University, Sabo, hosted ‘Sickle Cell Alma Awareness Wednesday’ to educate students on genotype compatibility before marriage.

 

The News Agency of Nigeria (NAN) reports the programme, with the theme ‘A holistic perspective on genotype compatibility’, held on Wednesday at Trinity University’s City Campus, Sabo Yaba, Lagos.

 

Convener, Oluwafemi Ajayi, said the initiative aimed to give back to society by promoting sickle cell awareness.

 

Ajayi stressed the need for genotype compatibility before marriage to prevent avoidable health and emotional challenges for families.

 

“Love should not blind you. Knowing your genotype with a partner is vital. Obedience to medical advice ensures healthier families and stronger societal contributions,” she said.

 

She urged persons living with sickle cell to build self-esteem and embrace their uniqueness.

 

“Never compare yourself with others. Despite challenges, you can contribute meaningfully to society,” Ajayi added.

 

Earlier, Prof. Clement Kolawole, Vice-Chancellor, TU said, advocacy for genotype compatibility must be prioritised nationwide to reduce sickle cell prevalence and end stigma.

 

Kolawole, represented by Dr. Isaac Fadeyi, Associate Professor of Mass Communication added that, “Informed choices, compassion, and sustained awareness will protect future generations and reshape Nigeria’s narrative.”

 

Dr Annette Akinsete, National Director of the Sickle Cell Foundation Nigeria, called for sustained advocacy to dispel myths linking sickle cell to spiritual beliefs such as ‘Ogbanje’.

 

“Education empowers families to make informed health decisions and correct harmful misconceptions,” Akinsete said.

 

She urged laboratories to ensure accurate genotype testing, backed by government regulation and legislative support for free treatment.

 

“Legislative backing can reduce the heavy burden on patients and families,” she added.

 

Dr Benjamin Adegunle of LUTH highlighted long-term impacts of sickle cell, urging adherence to evidence-based medical advice.

 

“Medical advice, inspired by God, must guide decisions to prevent sickle cell births,” Adegunle said.

 

Dr Ante Bassey of Isolo General Hospital warned that stigma could trigger depression, isolation and suicidal thoughts among patients.

 

“Awareness must extend to churches, mosques and communities to discourage discrimination,” Bassey said.

 

Caregiver, Mrs Abiola Alade, shared experiences raising two children with sickle cell, citing financial strain and emotional stress.

 

“Genotype compatibility must guide marriage decisions to prevent such hardships,” she said.

 

A Nursing Science student, Mr Daniel Oluwole, said the programme deepened his understanding of genotype testing.

 

“I now understand the importance of testing to avoid passing sickle cell to children,” he said.