Precious Endwell Sickle Cell Foundation
Supporting and representing people affected by sickle cell disorder
Who We Are
The Precious Endwell Foundation is a non-governmental and non –profit making organization dedicated to the sensitization, proper care and control of sickle cell disorder in Nigeria.
Our mission is to create better awareness and help improve the quality of life, and long-term outlook for individuals living with sickle cell disease through education, awareness and advocacy.
We are established to raise awareness and to help others with the disease with peer mentorship, education, advocacy, and other areas of support.
What We Do
01.
— Advocacy
We educate other Advocates, patients and families on the importance of understanding and managing the effects of Sickle Cell Disease
02.
— We Build Networks
We are proud to partner with a wide range of organizations to help provide a better quality of life for sickle cell patients. When we work together, we can increase our impact and service offerings.
03.
— Find Sponsors
We rely on your kind donations to keep doing the work we do. Every donation allows us to reach more people, run more activities, and improve the lives of those living with sickle cell.
04.
— We Educate
Promote Awareness in schools, churches etc., to sensitize people especially students on the importance of identifying and managing Sickle Cell Disease and those living with it.
05.
— We Provide Care
We organize or inspire community support for people living with sickle cell thereby bringing hope to the African child
06.
— We Counsel
We educate in issues surrounding compatibility so people carefully weight their decisions rightly
Impact Stories
Adam Osaro | Living with Sickle Cell is not a death sentence
Nigeria is believed to be the most sickle cell endemic country in sub-Saharan Africa with between 2% and 3% of the total population affected. I am really happy at the initiative Precious Endwell Sickle Cell Foundation is doing to sensitize the public
A Brighter Future — For Nigeria’s Children
Sickle cell disease had a significant negative effect on the quality of my life when growing up but through this foundation I am learning to live with it and help others look beyond the pain.
Partners
