The Causes Of Cystic Fibrosis And The Effects It Has On The Child And Parents

In infants symptoms include coughing, wheezing, excess mucus in the lungs, shortness of breath, extremely salty skin and decelerated growth. With infants it is very common for them to develop pneumonia infections because of all the bacteria that resides in the lungs. With treatment, most patients with cystic fibrosis live into their 20’s and 30’s, some individuals with milder cases can live longer. Death is most often due to end-stage lung disease.Thus far no cure for the disease has been found. Although, research on gene therapy is promising. Treatment is generally aimed at alleviating symptoms, preventing infections, and slowing the progress of the disorder. (Egan’s 10th Ed,

Cystic Fibrosis is a genetic disease which is progressive and limits breathing ability. The lungs and other organs are affected by a thick buildup of mucus. This mucus traps bacteria which leads lung damage, infections, and respiratory failure. The digestive enzymes being released is prevented, affecting the breakdown of food and nutrients being absorbed. ?More than 30,000 children and adults in the United States have Cystic Fibrosis. 70,000 people worldwide.? (Diagnosed With Cystic Fibrosis, Cystic Fibrosis Foundation) Someone who has Cystic Fibrosis have a defective gene from each parent which produces faulty protein. The CFTR gene is the gene that is mutated causing this. The channel that transports chloride in and out of cells is created by instructions that are created by CFTR gene. The regulation of chloride ions and water are prevented creating the thick mucus formed on the passageways of lungs, pancreas, and other organs. Cystic Fibrosis doesn?t cause learning problems are mobility of the person. Babies with this still develop and grow up normally. The average life expectancy is close to 40 years, and has been increasing in the last fifty years thanks to improved care. ?Chronic coughing, recurring chest colds, wheezing, shortness of breath, frequent sinus infections, and allergies that last all year, are the most common symptoms of Cystic Fibrosis.? (Cystic Fibrosis Symptoms) Since this disease is progressive

What is Cystic Fibrosis? How does it affect people living with it? Cystic Fibrosis, also known as CF, is a life-threatening hereditary disease. It is inherited by a faulty cystic fibrosis transmembrane conductor (CFTR) gene from each parent (Kowalczyk, 2014, p. 74). This faulty gene makes a defective protein that does not work well and causes the body to produce sticky, thick mucus and very salty sweat("About CF: Causes, Signs & Symptoms of Cystic Fibrosis,"

To begin, cystic fibrosis is a genetic disease that causes persistent lung infections and limits the ability to breathe over time. It is an inherited disorder both parents have to be a carrier of the gene. Some people say if a both parents have the gene then their is a 50% chance that the mother will have a baby with the disorder. It affect the

     Today, there is no cure for Cystic Fibrosis, but if the disease is found in an individual early enough, the patient can be recovered. About 85 to 90% of patients will have problems absorbing nutrients from their intestines. And because enzymes are lost when diagnosed, enzyme supplements are required to prevent bad nutrition and malnutrition. There are two main body parts that can be cared for the treatment of Cystic Fibrosis: The lungs and the chest. Lung problems can also be treated, but not cured. Antibiotics and other drugs may loosen the thick mucus in the lungs, but if it fails, a transplant lung may help to extend life. But about four hundred people die each year while waiting for a lung transplant. Also Chest physical therapy is a technique done by vigorous claps on the back and chest to loosen the thick mucus from the lungs. The average lifespan of an individual with CF is about thirty years.

Five year old Ellis Miles undergoes numerous treatments each day to counteract the symptoms that accompany cystic fibrosis including physiotherapy, pills containing digestive enzymes, and a treatment which breaks up the mucus in her lungs. Cystic Fibrosis has numerous life threatening symptoms and while there is no cure, there are several treatments that a typical patient undergoes each day to combat these symptoms. The most prominent symptom associated with Cystic Fibrosis is a thick mucus that clogs up tubes that carry out crucial roles in the human body. This mucus especially affects the respiratory tract. Mucus builds up in the respiratory tract making it difficult for individuals with cystic fibrosis to have a frequent cough that produces a thick

Cystic fibrosis is an inherited disorder that affects many functions of the body: breathing, digestion, and reproduction. The lifelong illness usually gets more severe with age and can affect both males and female equally. The symptoms and severity of cystic fibrosis differ from person to person. Most patients have both respiratory and digestive problems, while others only have respiratory problems. Intelligence is not affected in people with CF.

The main goal of any treatment for someone who has cystic fibrosis is to prevent and/or control lung infections, loosen and remove the mucus build up in the lungs, prevent and treat intestinal blockage and ensuring proper and adequate nutrition. If the treatment includes medications, antibiotics would be used to treat and/or prevent lung infections. To help get the mucus up and out of the lungs, mucus-thinning drugs will be used to improve lung function. By relaxing the muscles around the bronchial tubes, bronchodilators can help keep the airway open. Lastly are oral pancreas enzymes which help the digestive tract absorb nutrients. Non-medication treatments include chest physical therapy which helps the thick mucus loosen and in turn makes it easier to cough up. There is also something available called pulmonary rehabilitation which is something that can help improve lung function in an outpatient setting and this may include exercise training, nutritional education, breathing techniques to conserve energy and counseling and/or support groups. There are also several surgical procedures that can improve quality of life for patients with cystic fibrosis. These in removal of any nasal polys to help breathing, oxygen therapy to help prevent pulmonary hypertension or high blood pressure in the lungs, endoscopy and lavage treatments to

Cystic fibrosis generally affects mainly the lungs, pancreas, liver, intestines, sinuses, and the sex organs. People who have cystic fibrosis can have a variety of symptoms. Some people may only go through a few of them. Though, other people may go though more symptoms that later on can become very severe. One of the earliest symptom of cystic fibrosis that can be noticed beforehand is that the skin of a baby will have a salty taste when kissed. The rest of the symptoms happen later overtime as they start growing up. They affect the respiratory, digestive and reproductive system. One of the signs of cystic fibrosis in the respiratory system is the thick, sticky mucus that blocks the airways. Which causes bacteria to start growing and other infections too. This can also lead to frequent coughing, wheezing noises, and lung infections. Other problems may occur like sinusitis, bronchitis, and pneumonia, these can cause serious damage to the lungs. Cystic fibrosis affects the digestive system in many ways

The signs and symptoms of Cystic Fibrosis are going to involve the respiratory, gastrointestinal, reproductive and occasionally sweat glands. Usually we will see symptoms as early as birth as well as later in life. The very firsts signs of CF are noticed by parents on a new born child, when the child does not pass his stool(meconium) as well as a salty sweat in the forehead when kissed. (Health, 2013) Some relative sign and symptoms of the respiratory system include: cough, thick sputum, lung infections and sinus infections. The digestive system symptoms are a result of mucus blocking ducts and tubes. Constipation, stomach pain, Diarrhea, foul-smelling, greasy stools and poor weight gain are some of the main sings of CF. In the reproductive system females will have a hard time conceiving due to mucus in the cervix whereas males are considered infertile because they are born without a vas deferens tube. Other common signs and symptoms mostly seen with patient who have CF are salty sweat, fatigue, weakness, increased heart rate and decreased blood pressure.

Cystic Fibrosis, a very serious inherited genetic disease, is also known as CF and sixty-five roses. This disease affects one in every 3,000 live births. It may first appear in a newborn, but can appear all the way up until a young adult. However, ten percent of most cases are apparent at birth. CF affects the lungs and causes a build-up of abnormally thick mucus which leads to chest infections, and CF also affects the reproductive system. Doctors do not know what causes the mucus to thicken. CF’s infections usually lead to death in childhood and early adulthood. Most people infected with CF had a life span into their teens long ago. Now, due to advanced technology, the life span is in the fifties or older.

The symptoms that infants or kids may have if they have cystic fibrosis is nasal polyps, prolonged jaundice, severe malnutrition, and meconium ileus (bowel obstruction). The symptoms that are found in infants, children and adults are production of bulky foul smelling stools, chronic respiratory infections, constant coughing, nasal polyps, and persistent coughing yellow and green sputum. Other symptoms are coughing blood, recurrent: pneumonias, wheezing episodes. There are a bunch more symptoms these are just what most

Cystic Fibrosis, a genetic disease that is often considered progressive, affects a person's ability to breathe by causing frequent lung infections. A thick buildup of mucus in several organs such as the lungs and pancreas are caused by a defective gene in those with cystic fibrosis. This gene is inherited by either parent who carried the gene. In some cases, the buildup of mucus can cause respiratory failure or prevent the release of digestive enzymes that allows the body to break down food and absorb vital nutrients. Common symptoms to look for in people with cystic fibrosis are chronic coughing, frequent sinus infections, shortness of breath, salty tasting skin etc.

Cystic Fibrosis is a genetic life threatening disease that causes severe damage to the lungs and digestive system and slowly limits your breathing. What happens with CF is there is a large buildup of mucus in the lungs, pancreas, liver, intestines, sinuses, and sex organs. The mucus is usually made of sweat and digestive juices that are meant to act as lubricant but end up clogging up and blocking tubes, ducts and passageways. With the buildup of mucus it makes it easier for certain bacteria’s to grow, which make it easier for infections to start and spread, especially through the lungs. This in time can cause lung damage. When certain tubes get blocked it makes it to where your intestines cant fully absorb different nutrients

Envision needing to breathe through a straw consistently, for whatever remains of your life. This is the means by which people consistently feel while living with Cystic Fibrosis. Cystic Fibrosis is a deep rooted, genetic infection that influences numerous real organs. Sticky bodily fluid obstructs the aviation route in the lungs and in addition pathways leading to the digestive framework in the pancreas. This destructive illness has been examined for a considerable length of time with a strong desire for a cure. Advancements in technological innovations will clear the way for a better comprehension of Cystic Fibrosis, and, in addition, a significant improvement in lifestyle for patients.