Sickle Cell Disease Control: Engaging the Rural Dwellers

Day 2 – Ibadan South Zone, Batake/ Idiya Community, Ido LGA.  6th October, 2015.

Sickle Cell Disease Control: Engaging the Rural Dwellers

Sickle Cell Disease Control: Engaging the Rural Dwellers

Day 5 - Ogbomoso Zone, Ikoyi Ile Community, Orire LGA. 9th October, 2015.
Day 5 – Ogbomoso Zone, Ikoyi Ile Community, Orire LGA. 9th October, 2015.

At the various locations, the SCHAF team was led by its President, Professor A.G. Falusi. She delivered a lecture titled “Sickle Cell Disease Control: Engaging the Rural Dwellers”.  The lecture which was centered on prevention as a means of controlling SCD was relayed mostly in Yoruba Language to aid the understanding of the subject matter by all participants. The pattern of inheritance and complications of SCD were also emphasized with the aid of visual illustrations to make the people understand the way the disease is acquired, the plight of individuals living with the disease and the urgent need to control it.

Emphasis on Blood Genotype differentiation from Blood Group and the eventual importance of using these facts in mulling. Their own personal informed decision eventually in later life was emphasised. They were encouraged to learn more about SCD in the papers and the media as well as spread the word far and near. Parents were also encouraged to financially support their children in knowing their Genotype in proper places. Once done right, Genotype never changes with age.

SCHAF made her intentions clear on eventually coming back to launch a KNOW YOUR GENOTYPE ‘KYG’ Club in the various communities in the near future. The government and well-meaning Nigerians were called upon to support this programme towards ensuring that free Genotype testing is provided for every student at the secondary school level in the country. Several questions raised by the participants were answered which actually enriched the participatory and interactive programme.

  1. SCHAF provided handbills and fliers to further educate the community
  2. Parent handbooks for Sickle Cell Disease in Nigeria useful for the care of individuals living with the disease were provided to some free of charge.
  3. There was free Genotype Screening for some Senior Secondary School students at the locations visited were done.

Participants in the programme included all Local Chiefs, Government officials (State and Local), Community members, Health care professionals and invited Stakeholders, Secondary School Students and the National Youth Service Corp members.

Sickle Cell Disease is a family of disease which is Sickle Cell Anaemia (Hb SS), Sickle Cell Haemoglobin C disease (Hb SC) and some others such as Sickle Cell Haemoglobin F (HbS+F) etc.
Do you know that?

  1. 4 Million Nigerians have Sickle Cell Disease, Hb SS Sickle Cell Anaemia and Hb SC Sickle Cell Haemoglobin (Hb SS + Hb SC)
  2. 40 Million Nigerians have Sickle Cell trait. (Hb AS). These people are called Sickle Cell ‘Carriers’

What is your contribution to reduce the scourge of Sickle Cell disease in Nigeria?
Give us your Opinion and important links to whoever can help these affected individuals.


  1. […] Sickle Cell Hope Alive Foundation (SCHAF) in collaboration with the Oyo State National Youth Service Corps (NYSC) engaged the 33 local governments of Oyo State from the 5th to 9th of October, 2015 in a programme tagged “Health Initiative for Rural Dwellers (HIRD)”. The programme was designed to bring health care and health information to the doorsteps of the rural people who largely are not able to access such programmes. The 33 Local Government Areas were classified into 5 zones for the programme. Read more » […]

  2. ishaq - 28th December 2015

    …this is a very laudable effort from the SCHAF team entirely, in making the lives of Nigerian’s youth better by creating awareness n encouraging them to know their genotype… may Almighty God reward and bless the whole team abundantly, especially The President and founder of the organization, Prof.Adeyinka Gladys Falusi…more blessings…!!!

  3. Pharmacist Susan Sola Ayetoro - 19th June 2016

    It is a good initiative to create awareness for everybody living both in rural and urban areas. It is important for everybody to know their genotype and implications of getting married to a carrier when you know you are also a carrier. We need to be sincere with ourselves. God bless the coordinator and the team.
    I will like to be a member of the team.

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