IPF

Idiopathic Pulmonary Fibrosis (IPF) is a lung disease where the tissue connecting air sacs in the lungs becomes thickened and scarred over time, making it harder to breathe and for oxygen to pass into the bloodstream. "Idiopathic" means the exact cause is unknown. The scarring develops gradually, leading to symptoms like shortness of breath and a persistent cough. While there’s no cure, treatments can help manage symptoms and slow progression. IPF mostly affects older adults and requires medical monitoring to maintain quality of life.