Initiative takes fight against sickle cell disease to

Initiative takes fight against sickle cell disease to communities

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A non-governmental organisation, Nirvana Initiative and volunteerism, founded by a certified medical scientist accredited by the American Society for Clinical Pathology, with specialization in hematology and transfusion medicine, Modupeola Babawale, has received recognition from the YALI Network, for giving back to the community and making a meaningful difference in the lives of others by being selfless and using her resources to support her immediate community.

Speaking on her passion and Nirvana Initiative; she said “Nigeria has the highest number of individuals living with sickle cell disease, many of whom are either unaware of the condition or lack the means to manage it effectively. Through Nirvana Initiative, I work to ensure that everyone has access to vital information about sickle cell disease by conducting sensitization initiatives in strategic areas like schools, primary health care centers, and rural communities. We also provide free genotype testing to youths and intending couples. Additionally, I strive to make quality health care accessible to people living with sickle cell by partnering with hospitals to offer subsidized medical services, including wound care and routine lab tests. Recognizing that many warriors lack access to their basic routine medications, I ensure the provision of free essential medications to those in need.

On her motivation, she stated that “living with sickle cell myself, I’ve been fortunate to have access to excellent health care and a robust support system from a young age. However, I’m actually aware of my privilege and often think about those who lack these resources. This awareness compelled me to take action in my own way. Sickle cell is a complex and challenging condition, often perceived as a limiting disease. Despite my access to care, society still tends to view individuals living with it as less capable or weak. I believe that every warrior should have access to quality medical care, understanding, and support, as these are essential for improving quality of life. I also envision a society that is more accommodating and supportive of individuals with sickle cell. This belief motivated me to start the Nirvana Initiative in 2015.

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