Gene therapies are innovative medical treatments that aim to correct or replace faulty genes responsible for diseases. By introducing healthy copies of genes into a patient's cells, these therapies can potentially cure genetic disorders, such as cystic fibrosis or hemophilia. This approach focuses on addressing the root cause of the disease rather than just alleviating symptoms. One of the exciting aspects of gene therapy is its ability to use various techniques, such as CRISPR, to edit genes precisely. Researchers are continually exploring new ways to enhance these therapies, making them safer and more effective for patients. As technology advances, gene therapies hold great promise for treating a wide range of conditions.