Lives unaffected by cystic fibrosis

Life with CF

Cystic fibrosis is a genetic condition, which currently has no cure. With this in mind the focus of ongoing research is dedicated to improving the quality of life for people living with cystic fibrosis as well as advancing treatments to reduce symptoms and the affect they have on the body. 

While the details vary dramatically from person to person, living with cystic fibrosis (CF) is all about the routine. This routine can consist of one or two nebulisers every morning and every night with physio sessions in between plus up to 40 tablets per day including antibiotics some containing enzymes that aid in food metabolism.

On top of this there is the constant need to incorporate exercise into each day to keep the lungs active, making sure you eat enough nutrients and healthy fats to maintain a healthy body weight and avoid malnutrition.

Due to recent advancements in medical research there is now the option to treat people with CF from home and increase their quality of life.

For everyone with CF it is important to keep well rested and keep on top of things. Of course it’s harder for some than it is others, but vigilance is always key. If they let their guard down and don’t keep to their routine, people living with CF will find themselves in hospital. Hospitalisations can consist of at least two weeks and include procedures such as intense physiotherapy and strong antibiotics administered through an IV drip. People with CF can be admitted into hospital up to six times per year.

Outside of hospital there are specialist and CF specific clinics where people with CF visit regularly to be tested and monitor their health.

This information is just the basic outline of living with CF – there is far more to this disease and things only get more complicated when you introduce the complexities of family and professional life. CF is a full-time job. To learn more, visit our dedicated resource on CF Co-morbidities, the ‘CF Donut’.