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MUST Sickle Cell Disease Program and COBRA Agency Sickle Cell Services present the THIRD Annual Low country Sickle Cell Disease Symposium Ac UT e Ca r e M a nag even t i n Si ck LE Cell Di seas e
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To fill out sickle cell disease, you must follow these steps: 1. Consult a medical professional for a diagnosis 2. Understand the symptoms and complications associated with sickle cell disease 3. Stay informed about available treatment options 4. Follow a healthy lifestyle including a balanced diet and regular exercise 5. Take prescribed medications as directed 6. Monitor and manage pain and other symptoms 7. Attend regular check-ups with your healthcare provider 8. Stay educated and connected with support groups and resources for sickle cell disease patients

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Sickle cell disease primarily affects individuals of African, Caribbean, Middle Eastern, Eastern Mediterranean, and Asian descent. However, it can occur in anyone regardless of race or ethnicity. Individuals who have a family history of sickle cell disease or carry the sickle cell gene are at risk. It is important for pregnant women to get tested for sickle cell disease as it can be passed on to their children. People who exhibit symptoms such as anemia, frequent pain episodes, or complications related to sickle cell disease may need medical attention.
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Sickle cell disease is a genetic blood disorder that affects the red blood cells.
Healthcare professionals and organizations are required to report cases of sickle cell disease to public health agencies.
Sickle cell disease cases are typically reported through electronic medical records or directly to public health agencies.
The purpose of reporting sickle cell disease is to track and monitor the prevalence of the disease in a population.
Information such as patient demographics, medical history, and laboratory test results must be reported on cases of sickle cell disease.
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