Idiopathic pulmonary fibrosis (IPF) is a progressive and often fatal lung disease, which makes it difficult to breathe. Unfortunately, there is no cure for IPF at present, and the life expectancy of people with IPF can vary widely depending on various factors.
On average, people diagnosed with IPF typically survive for 3-5 years after diagnosis. However, some individuals may live longer with the disease, while others may experience a more rapid progression of the disease and have a shorter lifespan. Other factors that can affect life expectancy include age, overall health, and the severity of the disease at the time of diagnosis.
It is important to note that IPF is a complex disease and that each person’s experience with the condition is unique. Therefore, it is essential to work closely with healthcare professionals to manage symptoms and develop a treatment plan that is tailored to an individual’s specific needs.
