By Lucas Akol | Partner Relations Officer
Sickle Cell anaemia is a genetic disease with a power to change the identity of the patient. Carrier or Sufferer tag defines ‘how’ and ‘how long’ patient will live. The life expectancy of persons with sickle cell anaemia is reduced substantially due to limited medical resources available for tribal population. This disease is common in tribal community thereby making it all the worse due to lack of screening, diagnosis and right treatment. Some patients, however, can remain without symptoms for years, while others do not survive infancy or early childhood.
SCOEN’s regular screening camps and treatment proved very fruitful in limiting the severity of this fatal disease. Most patients suffer pain crises, fatigue, liver/spleen related disturbances and progressive tissue and organ damage. Impaired growth and development is the painful emotional trauma that is endured by parents and children with sickle cell anaemia.
We strongly feel that there is a Need to change the outlook towards patients of Sickle Cell Anaemia in the society. Any change begins with us as an individual. There are many things which an individual can help to sickle cell patients. Changing attitude and outlook towards their requirements is just the beginning.
Within camps we distributed free sweaters and blankets to the needy. Cold weather triggers their pain and hence greater chance of sickling crisis.
During this camp we received a special appreciation as district councils who visited our camp and appreciated our work. He also offered his full support for sickle cell awareness drive and treatment.
What you can do for Sickle Cell Patients:
We provide care and support to all those affected by Sickle Cell as well as other healthcare Support which include:
Your donations bringhope, love and bring smiles on the faces of sickle cell patients.
Please write to us for comments and for volunteering for fund raising activities.
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