Sickle-cell thalassemia is a genetic disorder that affects the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. It is a combination of sickle-cell anemia and thalassemia, both of which are inherited blood disorders.
Sickle-cell thalassemia can cause a variety of symptoms, including anemia, jaundice, pain, and organ damage. However, not everyone with sickle-cell thalassemia experiences acute crises, which are episodes of severe pain and other symptoms that can require hospitalization.
If you have sickle-cell thalassemia without crises, it is still important to manage your condition and monitor your health. Here are some tips:
It is also important to avoid any potential triggers that could cause a crisis, such as extreme temperatures, high altitudes, and stress. If you do experience any symptoms, it is important to seek medical attention right away.
In conclusion, if you have sickle-cell thalassemia without crises, it is still important to take care of your health and manage your condition. By staying hydrated, eating a healthy diet, getting regular check-ups, and avoiding triggers, you can help prevent complications and live a healthy life.
Sickle-cell thalassemia is a genetic disease that affects the production of hemoglobin, a protein found in red blood cells. This condition causes the red blood cells to become misshapen, leading to a range of health issues, including pain crises, anemia, and organ damage. While patients with sickle-cell thalassem...
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