Cystic Fibrosis Facts – 1,000 New Cases Annually
Cystic Fibrosis is a very common, inherited lung disease that causes extreme damage to your lungs, heart, pancreas and other internal organs. The damage caused by cystic fibrosis makes it impossible for a person to breathe. Cystic Fibrosis is genetic and most of the time occurs in the child through his or her grandparents.
However, this does not indicate that all children with cystic fibrosis will develop this chronic lung disease. Cystic Fibrosis (Cushing’s Syndrome) is a chronic lung disease that is characterized by excessive mucus production. Cystic fibrosis (CFS) is also called chronic fibrotic pulmonary fibroids (CFL).
It is one of the most common chronic respiratory diseases in the world. It causes dumping syndrome and can cause death if not treated. Cystic fibrosis syndrome may develop if a child has excess mucus inside the lower lungs and cannot drain off to the bathroom.
In fact, if a person has CFS, he or she may develop some of the following symptoms
- Experiencing extreme fatigue after physical or mental activities
- Feeling unrefreshed after a night’s sleep
- Reduced concentration
- Memory loss
- Dizziness that worsens with moving from lying down or sitting to standing
- Multi-joint pain without redness or swelling
- Frequent headaches
- Muscle or joint pain
- Tender and swollen lymph nodes in your neck and armpits
- Sore throat
Fatty bowel syndrome (FBS) is another common condition that occurs in people with cystic fibrosis
Fatty bowel syndrome is caused by excessive fat deposits inside the abdomen. Bowel movements are blocked by fat. Children with FBS may develop their fistula, which is a tunnel leading from the intestines into the bladder and rectum. Children with FBS may also suffer from dehydration, kidney stones, and malnutrition because of the lack of absorption of essential nutrients.
Leaky genes are another interesting cause of cystic fibrosis. This type of inherited abnormality results from a faulty gene that produces a molecule called amyloid protein. The amyloid protein is made from amino acids, and some amino acids, called “proteins”, link together in long chains.
Each chain has a definite sequence of letters, and these sequences are used to indicate what amino acid or letters are needed for a particular function in the human body. If one of these chains is missing, a person can inherit a defective gene from one of his or her parents.
This will most likely result in cystic fibrosis, although it may also result in other respiratory signs and symptoms, such as emphysema, asthma, chronic bronchitis, and sinusitis. The cystic fibrosis gene may also cause a few other types of genetic abnormalities, such as polycystic kidney disease and juvenile-onset diabetes.
The main symptoms of cystic fibrosis are the thick, sticky mucus inside the lungs.
The thick, sticky mucus makes breathing very difficult, causing breathing to become continuously laboured. In the past, doctors could only detect cystic fibrosis through the results of liver biopsy. However, with the advent of new medical technology, specialists are now able to diagnose cystic fibrosis by examining the inside of the lungs.
Through a lung biopsy, doctors are able to determine if a person has a distal intestinal obstruction syndrome or DIOS. A distal intestinal obstruction syndrome can cause swelling in the liver, which is noticeable through a distinct smell, as well as increased mucus production, breathing difficulty, and diarrhoea.
Furthermore, when a person has a DIOS, doctors can determine if the thick, sticky mucus is caused by an intestinal obstruction, or if the obstruction itself is causing the mucus to be thick and sticky. Due to the relatively new methods of diagnosing this disease, there are currently over 1,000 new cases being diagnosed every year.
This is due to more people being able to identify this disease and take control of it themselves, rather than turning to their doctors. Cystic Fibrosis is not a life-threatening disease, although it is important for patients to understand that should they develop symptoms, they should seek immediate medical attention.
Symptoms can include severe stomach pains, vomiting, fever, chronic diarrhoea, as well as lethargy, muscle fatigue, and chronic coughing. If you think you might have any of the symptoms of cystic fibrosis, it is important to talk to your doctor right away.
Your physician can perform a physical examination to determine if you have any of the symptoms listed above. If you do, there are many treatment options available, including medicines and surgical procedures. The severity of your symptoms will determine the course of treatment that is most effective.
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