4 natural treatments for cystic fibrosis ;
If I told you that there is a disease that some 12 million Americans currently have the gene for and that this same disease affects more than 30,000 children and young adults in the US, you might like to know about it, right? Of course it does, and that’s why you need to know about cystic fibrosis.
Cystic fibrosis (CF) is an inherited disorder that disrupts the normal functions of Epithelial cells , the cells that line the passageways of many of our most important organs – including the lungs and the respiratory system, liver, kidneys, skin, and reproductive system. People with CF have a particular defective gene that affects epithelial cell functions causing a buildup of sticky mucus inside the body experience, often leads to lung damage and chronic cough . This defect in turn affects how patients with CF breath and filter the air, food is digested and absorbed nutrients in the digestive tract. ( 1 )
Because epithelial cells have many important functions within the lungs, sweat glands and skin digestive system , CF symptoms can occur throughout the body and become serious. CF is a serious illness, chronic that needs to be managed appropriately throughout the patient’s life.
According to the Cystic Fibrosis Foundation, currently CF is considered however certain incurable interventions, dietary supplements digestive enzymes habits and style life can help control symptoms. ( 2 ) Fortunately, in recent decades the methods of treatment of cystic fibrosis have come a long way. Most people with cystic fibrosis now live in their 20s and 30s – and some even longer, until 40 or 50 years. Research shows early diagnosis of cystic fibrosis can help prevent complications and developmental issues, helping to improve the quality of life of patients.
Natural ways to help control cystic fibrosis
1. Early diagnosis and care
CF is most often diagnosed in unborn babies, newborns or young children through genetic testing. Doctors can now test for CF during pregnancy, which is especially common in children who are at high risk. In newborns or children, a “stress test” is now the most common to make a diagnosis of cystic fibrosis, which was conducted by analyzing a sample of skin sweat chloride levels for medium. Apart from a sweat test, chest x-rays, blood tests, tests of nutritional status, bacterial tests and lung function tests to measure breathing you can also be performed. ( 3 )
Early diagnosis of cystic fibrosis can help control symptoms and complications before they become worse, as dehydration and diarrhea , which may contribute to weight loss. doctors can help clear the lungs of mucus, helping to prevent infections, and get the patient started with a diet that will prevent nutrient deficiencies. Digestive enzymes and supplements can also help with healthy development and weight gain.
2. Dietary intervention to prevent deficiencies
Young patients with CF who begin a diet with nutrient-rich foods, supplements and digestive enzymes are more likely to have a strong metabolism, normal weight gain and prevent deadly infections. Diet plays an important role in the management of cystic fibrosis for lung infections and diseases progressing more slowly among children who are growing well and get enough vitamins, minerals, probiotics and antioxidants .
Many physicians / nutritionists who work with patients with CF recommend high fat, high calorie diet to reduce the risk of  malnutrition 19459024 , despite enzymes are often needed to promote absorption of fat and fat-soluble vitamins. Junk food and processed foods could be high in calories and fat (especially trans fats or omega-6 fatty acids found in refined vegetable oils, such as safflower, sunflower, corn, sesame), but you are generally not useful to decrease inflammation and prevent damage to the lungs, therefore, are not recommended for people with CF
Some of the beneficial nutrients that people with cystic fibrosis have more likely to be low include: ( 4 )
- vitamin K
- vitamin D
- vitamin E
- some people with CF might also need to add more salt to their diets to prevent [fatty[19459031dehydration]
- Omega-3 acids may be beneficial to reduce inflammation (found in fish caught in the wild, such as Alaskan salmon, sardines and halibut)
- pancreatic enzymes are also usually given to help digest food and the best calorie
- high quality multivitamins and antioxidants can help prevent inflammation, susceptibility to infections and lung damage
- probiotics [19459011supplements] are also useful for improving digestive functions
eat anti-inflammatory fats, including monounsaturated fats, such as oil extra virgin olive, avocado and virgin coconut oil , it is a good way to increase your calorie intake. Nuts and seeds such as almonds, chia seeds, flax seeds, walnuts and hemp seeds are also good choices for this purpose, as are meat more fat naturally as beef grass-red and lamb . unrefined carbohydrates can help provide dense calories and energy, especially when combined with fat, but it’s better than eating raw type, low glycemic index, such as grains, vegetables and fruits ancient starch.
3. Help with adequate lung function and breathing
treatments with cystic fibrosis today are mainly aimed at improving the quality of life and helps support nutrient intake / absorption, and improved respiratory and lung capacities. The use of medication treatments no pulmonary therapy to maintain lung function is very common and can be life-saving. Devices such as bronchodilator can help relax the muscles of the airways of the lungs, help expectorate mucus and prevent inflammation worse.
The use of certain inhalants and bronchodilators can help restore breathing and keep infections away, and can be used in devices called oscillatory positive expiratory pressure , which increase the flow air to the lungs through the use of vibrations that help break the mucus. ( 5 6 ) Research shows that approximately 50 percent of CF patients have some degree of bronchial lability (asthma) a bronchodilator can improve to increase the clearance breast secretions. Bronchodilators are sometimes used in combination with other therapies, such as anti-mucus physical therapy, medication and saline solutions or to expel phlegm and provide even more relief.
4. Physical therapy and exercise
Other natural methods to help CF patients breathe more easily include breathing exercises therapy physical and cupping therapy . These techniques do not require medication or antibiotics and help dislodge mucus chest, respiratory tract and elsewhere, limiting respiration and decreased quality of life.
Over the years, they have mixed opinions about whether physical therapy can be effective in reducing the symptoms of cystic fibrosis. A meta-analysis published in American Journal of Respiratory and Critical Care Medicine studied several different main approaches to eliminate bronchial secretions in the treatment of patients with cystic fibrosis. These approaches include positive expiratory pressure mask, forced expiration technique, exercise, autogenous drainage, and “standard physiotherapy” through vibrations, drainage and percussion. Them found that physical therapy worked very well in most patients, especially when used in combination with other approaches, such as gentle exercise, adequate.
More than 65 relevant trials eight review articles were included in the meta-analysis comparing independent techniques, and found that the standard physical therapy resulted in a significantly greater sputum expectoration than no treatment or other treatment alone. Physical therapy in combination with suitable for the patient exercise was associated with a statistically significant increase in the quality of life and lower increase CF symptoms. ( 7 )
Facts about cystic fibrosis
- CF affects more than 30,000 children and young adults in the US ( 8 )
- This disease is more common among Caucasians, while Asian Americans are the least likely to have CF. In the USA. about one of every 3,600 Caucasian children born with CF (compared with one in 17,000 African Americans and only one in 90,000 Asian Americans)
- The gene defected responsible for causing CF is in “chromosome No. 7 “of a person’s DNA. two copies of a CF gene (one inherited from each parent) are needed someone to develop CF. When two CF carriers have a child, there is a one in four chance that the child will have CF
- CF can also be performed on people who do not develop the disease if they inherit only one CF gene. The carrier matrix can then transmit the disease to their children, and estimates show that about 12 million Americans are currently carriers of cystic fibrosis.
- 85 percent of people with CF are diagnosed in childhood. Today, early detection, even during pregnancy, is helping doctors to control the disease as soon as possible.
how cystic fibrosis develops
CF affects how certain proteins function in the epithelial cells of the mucous glands. Most people think of epithelial cells in terms of skin – as they do, in fact, helps us to perspire so we can regulate our body temperature. But these important cells also have the responsibility to control the way chloride (part of natural salts) passes through cell membranes in other parts of the body as well. Epithelial cells balance the ratio of salt to water, forming the important fluids, digestive juices and mucus that help break down food and prevent viruses or infections. ( 9 )
With CF, thick mucus begins to accumulate and can begin to block the airways in the lungs, contributing to recurrent infections because germs are more likely of being trapped inside the body. Besides this mucus damage the lungs and reduced immunity, is also able to affect the digestive system, especially pancreas, kidneys, intestines and liver. Mucus may start slowing the production of important digestive enzymes and “juice” which normally are secreted by the pancreas, which leads to problems properly absorb nutrients in the intestines and weight loss sometimes unhealthy.
The symptoms of cystic fibrosis
People with cystic fibrosis suffer from symptoms including: ( 10 )
- nasal congestion, lung damage, chronic cough and  asthma-like symptoms ; cough that produces thick, heavy, mucus discolored
- sinusitis and repeated lung infections (such as bronchitis and pneumonia which it is a major cause of a shorter life)
- difficulty breathing or wheezing, even when at rest
- nutrient deficiencies, especially of fat-soluble vitamins (vitamins a, D, e and K)
- developmental problems in infants and children
- weight loss sometimes dangerous unintended
- diarrhea, dehydration and electrolyte imbalance
- oily, bulky stools (caused by undigested fat and protein accumulates in the stool)
- digestive problems such as intestinal gas, swollen belly , chronic diarrhea and abdominal pain
- salt “merengue” on the skin (caused from epithelial cells will not be able to balance salt and water)
- fatigue chronic
- long -term complications and diseases that can develop from CF include: sinusitis , bronchiectasis , pancreatitis , bowel obstructions, nasal obstruction, collapsed lungs ( pneumothorax ), rectal prolapse , gallstones, diabetes and low density bone
Because many cases of cystic fibrosis are diagnosed in infants or very young children, developmental problems and life-threatening infections are some of the biggest concerns. Many babies born with CF do not gain weight as expected because the mucus prevents pancreatic digestive juices from entering the intestines and breakdown of fats and proteins properly. The lungs are particularly susceptible to recurrent, such as bronchitis or pneumonia, sometimes infections, babies or small children are not able to fight.
The causes of cystic fibrosis
Cystic fibrosis is a hereditary disease caused by a defective gene that directs the way the body produces a type known as CFTR (CFTR) protein. CFTR is found in the epithelial cells of the body, which are more abundant in the lungs, digestive tract, sweat glands and the genitourinary system (the system of organs of the reproductive organs and urinary system).
CFTR proteins help epithelial cells regulate levels of to chloride in the salt (sodium chloride), so that when not working normally, the consistency of the mucus and other fluid levels is altered in a dangerous way. The delicate balance of salt and water needed to maintain a thin layer of mucus within the organs moves, and as a result, a thicker than normal strongly coats the inside of the lungs and passages mucus is formed.
mucus in the lungs has the important function of trapping and helping to kill germs, such as bacteria, viruses and fungi. In individuals without cystic fibrosis, I mucus is normally thin and similar fluids, which allows easily rubs the respiratory system, carrying with it the germs and waste, which are then removed from the lungs. However, when someone has CF, “sticky” mucus remains lodged in the ducts of the lungs, unable to eliminate potentially dangerous germs.
CF causes the most damage to the lungs, but also impairs the normal digestion. In the pancreas and intestines, thick mucus can block how important enzymes function, changing the way food is digested and absorbed nutrients. Many people with CF have difficulty eating and digest food normally, especially children who are likely to slow development, nutrient deficiencies and low weight gain. Even if cystic fibrosis does not change the intake of appetite and food from someone, you can still block some nutrients are absorbed.
Future Care for cystic fibrosis
Rather than simply treating the symptoms of CF, new approaches are seeking to target the underlying genetic causes. ( 11 ) Several new treatments are being developed for CF that offer great hope for the future.
A treatment that has already been used successfully in more than 100 patients with CF in the US is an inhaled aerosol containing normal copies of defective CF gene, which can correct the defective copy in the lungs and improve how mucus becomes. A similar approach is therapy repair protein, which also addresses how the defective CFTR protein functions and reduces the accumulation of sticky mucus in the digestive tract and airways.
Cystic Fibrosis Takeaways
- Cystic fibrosis affects more than 30,000 children and young adults in the US
- When two CF carriers have a child, there is a one in four chance that the child will have CF CF can also be performed on people who do not develop the disease if they inherit only one CF gene. The carrier matrix can then transmit the disease to their children, and estimates show that about 12 million Americans are carriers currently CF
- Most people with cystic fibrosis now live in their 20s and 30s – . And some even longer, in their 40s or 50s. Research shows early diagnosis of cystic fibrosis can help prevent complications and developmental issues, helping to improve the quality of life of patients.
- The best ways to manage naturally cystic fibrosis include diagnosis and early care, dietary intervention to prevent deficiencies, help with lung proper function and breathing, and physical therapy and exercise
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