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Fight Sickle Cell Disease in Angola. Support the Cure2Children Foundation

Cure2Children was invited to Luanda, by Dr Luis Bernardino, co-founder and former director of the David Bernardino Hospital, the only Children's hospital in Angola. We got connected to Luis over a year ago at a meeting organized by the Mediterranean Institute of Hematology in Rome.
 
The scope of our trip was to explore the possibility of setting-up a bone marrow transplant service in Luanda, the capital city of Angola, that would focus on curing children with sickle-cell disease. 20% of the population is a carrier and 1.5% of new-borns are born with the disease. David Bernardino Hospital follows over a thousand cases and has a very busy clinic, but doesn’t yet have the capacity and knowledge of how to offer a cure, locally, and affordably.
 
We then met with the Ministry of Health, Hon. Jose Vieira Dias Van-Dunem, and Vice Minister Hon. Carlos Alberto Masseca to seek their cooperation in our mission to help children suffering from sickle-cell disease in Angola
 
Sickle-Cell Disease (SCD):
 
Sickle-cell disease is a group of disorders that affects hemoglobin, the molecule in red blood cells that delivers oxygen to cells throughout the body. People with this disorder have atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape.
 
Signs and symptoms of sickle-cell disease usually begin in early childhood. Characteristic features of this disorder include a low number of red blood cells (anemia), repeated infections, and periodic episodes of pain. The severity of symptoms varies from person to person. Some people have mild symptoms, while others are frequently hospitalized for more serious complications.
 
The signs and symptoms of sickle cell disease are caused by the sickling of red blood cells. When red blood cells sickle, they break down prematurely, which can lead to anemia. Anemia can cause shortness of breath, fatigue, and delayed growth and development in children. The rapid breakdown of red blood cells may also cause yellowing of the eyes and skin, which are signs of jaundice. Painful episodes can occur when sickled red blood cells, which are stiff and inflexible, get stuck in small blood vessels. These episodes deprive tissues and organs of oxygen-rich blood and can lead to organ damage, especially in the lungs, kidneys, spleen, and brain. A particularly serious complication of sickle cell disease is high blood pressure in the blood vessels that supply the lungs (pulmonary hypertension). Pulmonary hypertension occurs in about one-third of adults with sickle cell disease and can lead to heart failure.
 
On August 26, we visited Girasol Hospital, a very nice and well-equipped hospital run by Dr Antonio Filipe, a well-known cardiologist. Developing a transplant program seems part of their strategic objectives.

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Posted by: Cure2Children