Cystic Fibrosis (CF) is the most common, genetically acquired, life-shortening chronic illness affecting young Australians today. Understand the risks, the effects and how to best live your life.
Mercedes Krasznai's insight:
An interesting fact about Cystic fibrosis is that it is the most common life threatening genetic condition in Australia. Right now, more than one million Australians carry this gene and one in every 25 people carry it around unknowingly. Fortunately it is not contagious, only genetic. However, most people dont know they have it and pass it on to their children.
Some signs and symptoms of Cystic Fibrosis would be difficulty breathing, coughing, lung infections, large of amounts of mucus, failure to grow or gain weight, extreme difficulty digesting food, wheezing, and breathlessness. However, these symptoms may vary with each person, and the severity of the disease. New born babies are now screened for cystic fibrosis and diagnosed earlier to prevent it from getting worse. People with cystic fibrosis also may have higher level of salt than most people, so when parents kiss their children and taste salt, there is a chance of them having cystic fibrosis.
Cystic fibrosis is a genetic disorder that cannot be prevented. However, people who have cystic fibrosis can help prevent more serious health problems such as lung infections by: Keeping immunizations current.
Mercedes Krasznai's insight:
Since Cystic fibrosis is a genetic disease, it cannot be prevented. Some people who are dealing with it however, have the ability to lower the risk of making it a serious problem in the future. The first thing they can do is get vaccinations to keep their immune system and help stabilize the symptoms. People should also avoid smoking and secondhand smoke because the harsh chemicals can build up inside the respiratory system and start damaging it. Eating nutritious, high-calorie food would be wise to maintain growth and absorption of nutrients. People could go for nutritional and respiratory therapy as well and can use the airway clearance technique to move the thick mucus from the lungs. Over the years however, treatments have improved greatly over the years.
CF is caused by a mutation in the gene for the proteincystic fibrosis transmembrane conductance regulator (CFTR). This protein is required to regulate the components of sweat, digestive fluids, and mucus. CFTR regulates the movement of chloride and sodium ions across epithelial membranes, such as the alveolar epithelia located in the lungs. Although most people without CF have two working copies of the CFTR gene, only one is needed to prevent cystic fibrosis due to the disorder's recessive nature. CF develops when neither gene works normally (as a result of mutation) and therefore has autosomalrecessive inheritance.
Cystic fibrosis is a genetic disorder that appears in some humans. It mostly affects the lungs and also the pancreas, liver, and intestine. They are like little scars or cysts that are formed by an unnatural transport of chloride and sodium across an epithelium. There many symptoms but the most common one is difficulty breathing which results from frequent lung infections. Other symptoms include; sinus infections, poor growth, and infertility. Cystic fibrosis is caused by the mutation in the genes for the protein cystic fibrosis, which is required to regulate sweat, digestive fluids, and mucus. This thick, abnormal mucus clogs the lungs and creates a breeding ground for bacteria, leading to life-long lung infections.
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