Sickle Cell and Complications : Prevention Measures and Interventions
Sickle cell disease (SCD) is a genetic disorder that affects the production ofhemoglobin, a protein that carries oxygen throughout the bodyPeople with SCD are prone to experiencing frequent complications such as infections, pain, and even organ damage. Preventive measures and early intervention can help manage these complications and improve outcomes for people living with SCD.Here
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Understanding The Importance of Psychological Education for Families of Sickle Cell Patients
Sickle cell disease is like a puzzle that affects both the body and the mind. Beyond theawareness of the disease, it is important to emphasize the importance of educating patientsand their families on managing through the pain, emotions, general treatment, and care. Whena family faces the challenges of sickle cell disease, the journey can be
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Empowering Sickle Cell Patients and their Families
Advocacy and support groups create a win-win situation by playing a critical role in educating and empowering sickle cell patients and their families. These groups provide a safe place for people with sickle cell disease (SCD) to connect with each other, exchange ideas, support one another, and advocate for better care and treatment for themselves.
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Etiology, Epidemiology and History of Sickle Cell anaemia
Sickle cell anaemia is a part of a group of diseases referred to as sickle cell disease or SCD for short. These are diseases that affect the haemoglobin in the body, the molecule within red blood cells that are responsible for the delivery of oxygen.
Read MoreWhy You Should Care about Sickle Cell anaemia
Globally, more than 100 million people carry the sickle cell trait. The concentration of trait holders is very high in places like Africa, the Caribbean, South America and within Black communities worldwide. It is a big part of many people’s lives, and there isn’t any simple solution to the disease. Even if you are not
Read MoreOrigins of Sickle Cell anaemia
Where did Sickle Cell anaemia originate, and when and how did it come about? Sickle Cell disease originated in Africa, where it is still prevalent today. Information from the gene leads us to know that SCD originated from 5 mutations, 4 of which came from the continent of Africa. These mutations led to the genes
Read MoreWhat is Sickle Cell Anemia?
What is Sickle Cell anaemia? (brief overview) Sickle Cell anaemia falls under a group of disorders referred to as Sickle Cell Disease. It is a hereditary disease that affects the red blood cells in your body. This causes the body to have an insufficient amount of red blood cells to oxygenate the body. People of
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