*SICKLE-CELL DISEASE AND STEM CELLS TREATMENT*

Sickle-cell disease (SCD) is a group of blood disorders typically inherited from a person's parents.

The most common type is known as sickle-cell anaemia (SCA). It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. This leads to a rigid, sickle-like shape under certain circumstances.

Problems in sickle cell disease typically begin around 5 to 6 months of age. A number of health problems may develop, such as attacks of pain ("sickle-cell crisis"), anemia, swelling in the hands and feet, bacterial infections, and stroke.

*When treated with stem cells, patients have reported revitalized hemoglobin levels and a longer lifespan because stc30 will build health cells in the blood.*

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