One of the major genetic diseases in the region of Africa is the sickle cell disease also known as SCD. World Health Organisation has been supervising and take appropriate measures for sickle cell disease prevention since the last decade. From primary prevention to ongoing support, WHO has been working in this part of the world in order to improve the quality of life of people living there.
A genetic blood disorder that impacts the red blood cells count and the haemoglobin is known to be sickle cell disease. Individuals who are diagnosed with it have to bear a very drastic change in their life and everything changes for them whether its their education, work, daily or social life.
It is an extremely widespread illness in major parts of Africa as well as in Middle Eastern region. In those countries, where SCD is widespread and poses a great threat to the human health, some sort of control and public health programmes are in operation. Unfortunately, those areas where systematic screening is not under progress the diagnosis of this disease is usually done when the most severe complications start to occur.
A blood test is done in order to identify SCD which is a very simple and easy process. It becomes possible to treat a patient effectively if the diagnosis is done during the early stages. If the major cause of this particular infection is prevented and the patient undergoes proper counselling, then this illness can be eliminated completely. It is a very sad thing that children who are affected by this severe illness do not even reach the age of five.
With regards to finish cure, there is no such thing for SCD. Still, if preventive measures are taken after and medication is carried out, one can stay healthy. With the assistance of legitimate prescriptions, great admission of sustenance and liquids, great well being might be kept up for a more extended time period. Blood transfusion and surgery gets vital in situations where the sickness advances.
Prevention can be possible if the screening is essentially done in high risk countries. The ideal time to identify the disease is during prenatal screening or at time of birth. If counselling is done and people are made aware of such screening, its most likely that the number of children who are born with this illness could be reduced to a great extent.
The programmes for SCD screening can be too expensive sometimes, this is the reason why not many countries run this programme very often. There is dire need for such techniques that would make the screening and diagnostic process much less complicated and affordable at the same time. At the moment, not many governments can afford to run the prevention programme as it is too expensive.
In order to generate new information and carry out research regarding SCD, a specialized approach must be taken by the authorities like WHO in order to ensure proper preventive measures are being taken by the high risk countries. Its really important that the community members get familiar with the risks and the preventive measures that can be taken with regards to SCD.
A genetic blood disorder that impacts the red blood cells count and the haemoglobin is known to be sickle cell disease. Individuals who are diagnosed with it have to bear a very drastic change in their life and everything changes for them whether its their education, work, daily or social life.
It is an extremely widespread illness in major parts of Africa as well as in Middle Eastern region. In those countries, where SCD is widespread and poses a great threat to the human health, some sort of control and public health programmes are in operation. Unfortunately, those areas where systematic screening is not under progress the diagnosis of this disease is usually done when the most severe complications start to occur.
A blood test is done in order to identify SCD which is a very simple and easy process. It becomes possible to treat a patient effectively if the diagnosis is done during the early stages. If the major cause of this particular infection is prevented and the patient undergoes proper counselling, then this illness can be eliminated completely. It is a very sad thing that children who are affected by this severe illness do not even reach the age of five.
With regards to finish cure, there is no such thing for SCD. Still, if preventive measures are taken after and medication is carried out, one can stay healthy. With the assistance of legitimate prescriptions, great admission of sustenance and liquids, great well being might be kept up for a more extended time period. Blood transfusion and surgery gets vital in situations where the sickness advances.
Prevention can be possible if the screening is essentially done in high risk countries. The ideal time to identify the disease is during prenatal screening or at time of birth. If counselling is done and people are made aware of such screening, its most likely that the number of children who are born with this illness could be reduced to a great extent.
The programmes for SCD screening can be too expensive sometimes, this is the reason why not many countries run this programme very often. There is dire need for such techniques that would make the screening and diagnostic process much less complicated and affordable at the same time. At the moment, not many governments can afford to run the prevention programme as it is too expensive.
In order to generate new information and carry out research regarding SCD, a specialized approach must be taken by the authorities like WHO in order to ensure proper preventive measures are being taken by the high risk countries. Its really important that the community members get familiar with the risks and the preventive measures that can be taken with regards to SCD.
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You can visit www.sicklesafety.com for more helpful information about Sickle Cell Disease Prevention And Cure.
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