Measures Of Sickle Cell Anemia Prevention

By Coleen Torres


This type of sickle cell disease is one in which the patient body produces sickle-shaped red blood cell. There are no known scientifically proven ways of sickle cell anemia prevention besides measures precautions that have proven to increase and improve length and quality of the lives of the patients of this type of sickle cell disease.

This measures range from regular body checkups according to the recommended time frame of between 3-6 months, drink sufficient fluids to avoid dehydration and avoiding smoking or staying in smoky areas. Patients should be re relaxed and should also avoid crowded places and strenuous activities besides having thorough and timely eye examinations.

Childhood and adulthood vaccinations against common andor opportunistic ailments should be adhered to strictly for patients as it should be for each and everyone. Childhood procedure for immunization for example the vaccine against pneumonia, influenza and meningitis amongst others ought to also be administered fully and the required time and age. Pneumococcal and meningococcal vaccines are vaccines against pneumonia and meningitis administered to children respectively.

Patients should undergo an annual skin test for tuberculosis. Prolyphalytic antibiotics should be administered to prevent common but serious and opportunistic ailments found in juveniles and patients of these anemic diseases. These drugs are like the penicillin which is administered to anemic patients between 2 months and 5 years of age.

Diet and nutritional measures are also very important in preventing occurrences of this disease. Patients ought to avoid dehydration by taking in enough fluids each and every day. Patients should also adhere to a strict dietary and supplement procedures. Foods rich in minerals, vitamins, proteins, fats and calories should be their choice of ingestion. Examples of such foods are soybeans, fruits like watermelons, meat, poultry, bananas and plantains among others.

Childhood and adult patients are prone to stress related diseases like depression as a result of stigmatization, poor medical service and facilities among others. High cost of treatment is also a cause of stress related diseases that can be reduced by communal health care for this patients and proper hospitalization and medication. Patients and their care takers should make sure that they acquire stress free environments and support them both physically and emotionally in their day to day lives.

Additionally dealing with this long term disease can be achieved by meditation, breathing exercises, embracing positive thinking in order to acquire copying skill and reduce pain that is experienced by these patients. Today online platforms are available to all for research and connecting with support groups. Beside that one could rely on his her parents for support and also acquire professional help which is cheaper and more convenient.

In conclusion sickle cell anemia patients can live a normal and quality life by adhering to strict nutrition methods, avoiding stress and strenuous activities, having positive support from members of the community and like everyone else in the community they should have lifelong goals and ambitions besides engaging themselves in humorous social activities in their each and every days lives.




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