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Understanding Cystic Fibrosis

Aug 11, 2008
This type of problem that many individuals suffer from is generally inherited from each of the child's parents. The parents can both be a carrier of CF and not actually suffer from the disease themselves. When both the mother and the father is a carrier of the gene that causes CF, it will also mean that it can be transferred to the baby and causing them to be born with this disease.

When an individual suffers from having Cystic Fibrosis or CF, it will make their body produce thick mucus, which can cause the lungs to become clogged. They will also experience problems in the digestive system. The thick mucus produced can clog up the passageways in the reproductive organs, pancreas, stomach, liver, and the intestines as well. Because of this, it will generally make it much more difficult for individuals to digest their food properly, or be able to receive all of the vitamins and nutrients that their body needs to be able to stay healthy.

The thick mucus that is produced also makes a perfect spot for bacteria to grow, and this can cause the patient to endure the problem of infections. Depending on each individual person, cases of CF can be either mild or severe. Another problem with CF is the special protein that our body's need in making normal mucus is defective. This ultimately will cause the problems that individuals will experience in having CF.

Researchers are constantly at work to try to find a cure for this disease, and for better treatments. Until this happens, it is very important for parents to stress to their children who suffer from having this disease, the importance of taking care of their health as best they can.

Cystic Fibrosis symptoms

The symptoms of Cystic Fibrosis are not always something that can be seen when a baby is first born. Symptoms can sometimes take a while before they will develop in some individuals. One symptom a baby may experience that will alert doctors to suspect CF would be if a baby were to experience several lung infections, or if the baby coughs more than normal. Another red flag for this disorder would be bulky bowel movements that are unusually large. The baby may also have problems in being able to gain the normal amount of weight that is expected. To find out for sure if a baby has CF, the physician will do a simple and painless test that involves collecting a small amount of sweat, then testing it to determine how much salt it contains. Children that have Cystic Fibrosis have larger amounts of salt in their sweat than other children without the disorder.

Although there are no known cures for cystic fibrosis, the problem can be treated in a controlled manner through physiotherapy, nutrition, exercise. for example, the physiotherapy would involve a process of clearing the lungs. for nutrition, it is recommended the sufferer takes something that helps to make food easy to digest.
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