Hemophilia A is a genetic disorder that affects the blood's ability to clot. It is caused by a deficiency of a protein called factor VIII, which is essential for blood coagulation. People with this condition may experience prolonged bleeding after injuries, surgeries, or even spontaneous bleeding episodes. This can lead to serious health complications if not managed properly. Treatment for Hemophilia A often involves regular infusions of factor VIII to help prevent bleeding episodes. Patients may also receive medications to enhance clotting. With proper care and management, individuals with this condition can lead active and fulfilling lives.