Why do people with cystic fibrosis find it hard to digest there food?

Cystic fibrosis (CF) is a genetic disorder that affects the mucus and sweat glands. The thick mucus clogs the airways, leading to chronic lung infections and respiratory problems. It also affects the function of the pancreas, an organ that helps digest food.

In CF, the pancreas does not produce enough pancreatic enzymes, which are necessary for breaking down proteins, fats, and carbohydrates in food. Without these enzymes, the food is not properly digested and absorbed, leading to malabsorption.

Symptoms of malabsorption in CF can include:

- Diarrhoea

- Steatorrhea (fatty stools)

- Bloating

- Gas

- Abdominal pain

- Weight loss

- Vitamin and mineral deficiencies

To manage malabsorption, people with CF need to take pancreatic enzyme supplements with their meals. These supplements help break down the food and allow the body to absorb the nutrients. They also need to follow a healthy diet and take vitamins and minerals supplements to prevent deficiencies.

With proper treatment and management, people with CF can live a relatively normal life and achieve good nutrition.