Sickle Cell in Africa
Medicines and hospital admissions are essentially the lifeline to children and young people living with this genetic blood disorder - Sickle cell anaemia.
Unfortunately, many families in Africa are not able to afford the costs of these drugs and hospitalization, thus many children become overwhelmed by minor infections that cause more organ damage or terminate their lives.
We would like to appeal to you to help us to raise funds to purchase these essential drugs and equipment that will essentially be prolonging and saving lives of children and young people.
Young people are labeled ‘Sicklers’ which is demeaning and leads to low self-esteem and suicidal thoughts. These are just a few the difficulties children, young people and their families have to face day by day.
Our ambition is to ensure that children, young people and their parents/carers have a voice and governments of affected countries make a positive change in their lives.