Cystic fibrosis is a type of genetic disease that causes the mucus in the body to become thick and sticky, thus clogging the ducts in the body. As a result of this blockage, some organs, especially the lungs and digestive system, are disrupted, even damaged.
Causes of Cystic Fibrosis
Cystic fibrosis is caused by a defect or mutation in a gene, the gene that regulates the transmembrane conductance of cystic fibrosis, which alters proteins that regulate the movement of salts into and out of cells. As a result, the mucus becomes thick and sticky in the respiratory, digestive, reproductive systems, as well as increased salt in sweat.
Children need to inherit one copy of the gene from each parent to develop the disease. If children inherit only one copy, they will not develop cystic fibrosis. However, they will become carriers and be able to pass on the gene to their own children.
Symptoms of Cystic Fibrosis
The signs and symptoms of cystic fibrosis vary, depending on the severity of the disease. However, usually children with this congenital disease have higher levels of salt in their sweat. Parents can often feel the salty sweat when kissing their child. Most of the signs and symptoms of cystic fibrosis affect the respiratory and digestive systems.
Here are some respiratory symptoms that can occur as a result of cystic fibrosis:
- Prolonged cough.
- Shortness of breath or difficulty breathing.
- Inflamed nasal passages or nasal congestion.
- Recurrent sinusitis.
Coughing occurs when the body tries to clear the lungs of thick mucus, and this symptom is the most common. In addition to the above symptoms, lung infections are also prone to be experienced by people with cystic fibrosis. This infection can become more severe and potentially contagious among fellow patients with cystic fibrosis due to bacterial overgrowth.
In the digestive system, the pancreatic ducts can also be clogged by mucus. With the blockage of the pancreas, the automatic digestive enzymes produced by these organs can not reach the intestines to help the process of digestion of food. That is why patients with cystic fibrosis who have disorders of their digestive system will experience symptoms such as:
Weight loss or even growth that is inhibited due to food that is not digested properly so that patients are malnourished or malnourished.
The texture of the stool is lumpy, greasy, and has a pungent odor.
In newborns, cystic fibrosis can clog the process of early excretion of feces or meconium that generally comes out on the first or second day of birth.
The thick black stool becomes difficult to pass through the intestines because the texture changes to become denser. This condition is called meconium ileus and can only be treated through surgery. In addition to meconium ileus, babies born with cystic fibrosis are also prone to symptoms of jaundice.
The Tole Herbs Treatment
Cystic fibrosis treatment with TheTole herbs method guarantees cure in most cases of cancer, especially if the patient seeks the Tole herbal remedies and acupuncture techniques during the early stages of cystic fibrosis. Like allopathic treatments, the Tole method also relies on patient's medical history, type and stage of cancer and other characteristics like age and health of the person for treatment purposes. However, where it differs is in the use of natural, herbal methods for treatment instead of chemical drugs or painful chemotherapies or radiation.
Experts at the Tole Medical Center study each patient's medical records and under the guidance of herbal medicine expert, Dato' Master Tole devise herbal formulations tailored to each person's needs. The Tole medication has an impressive track record and statistics for patients with diseases that are hard to treat. Over recent years, it has branched out into treatment for cancer patients of all sorts and already has amazing testimonials and reports from patients benefitting from their treatment.
For cystic fibrosis patients who are skeptical about the benefits and side-effects of normal medication routes, cystic fibrosis treatment with the Tole Center's guidance can indeed be the best alternative. And because of the fact that it guarantees a cure to patients who follow its herbal remedies and are only in their early stages of cystic fibrosis, it is definitely worth checking out.
