For patients who have cystic fibrosis, it’s important to understand that this medical condition is inherited and it causes serious damages to the digestive system and lungs. Besides, it affects those cells that produce sweat, mucus, and digestive juices, which are the fluids that are slippery and thin normally. Defective genes cause this kind of secretion to become sticky and thick so that it plugs up ducts, tubes, and passageways instead of acting as a lubricant, especially when it comes to lungs and pancreas.
Although this disease requires daily care, people with cystic fibrosis can attend work and school while having a decent quality of life. Think about certain improvements in treating and screening because they allow patients to live up to their 50s. The good news is that the screening of all newborn babies for cystic fibrosis is performed in all states so that this medical condition is easy to diagnose at the very beginning, even before any dangerous symptoms develop.
It’s important to know the symptoms and signs of cystic fibrosis, but you should understand that they may vary considerably based on its severity. Even in the same patient, symptoms may both improve and worsen, while some people may not have any symptoms until their adulthood or adolescence at all. For example, those patients who have cystic fibrosis have a high level of salt in their sweat, and other widespread symptoms usually affect their digestive and respiratory systems. Keep in mind that adult patients are more likely to develop special atypical symptoms, including diabetes, pancreatitis, infertility, and others.
When it comes to respiratory symptoms and signs, they include wheezing, exercise tolerance, breathlessness, persistent coughing, regular lung infections, sticky and thick mucus, inflamed nasal passages, etc. Don’t forget about important digestive symptoms and signs that include greasy and foul-smelling stools, severe constipation, intestinal blockage, and others.
It’s necessary for patients to know when to see their doctors. Once you notice any of the above-mentioned symptoms, you need to go to the hospital to be properly examined and diagnosed. In conclusion, there are different defects that may occur in genes, and everything depends on the severity of this health condition. People need to inherit one copy of the defected gene from every parent to develop this disease. If they have only one copy, they will be carriers.
For patients who have cystic fibrosis, it’s important to understand that this medical condition is inherited and it causes serious damages to the digestive system and lungs. Besides, it affects those cells that produce sweat, mucus, and digestive juices, which are the fluids that are slippery and thin normally.