- BY Dr. Rajeev's Clinic
Cystic fibrosis is a genetic disorder that damages your lungs, pancreases digestive tract and other organs. It's an inherited disease caused by a defective gene that can be passed from generation to generation. Cystic fibrosis affects the cells that produce mucus, sweat and digestive juices. Mucus should be thin and slippery but when you have Cystic Fibrosis it becomes thick and glue like. this blocks tubes and ducts throughout our body. this thick mucus builds up inside our body airway. This makes it hard to breathe. the mucus traps germs and leads to infections.it can also cause sever lung damage like cysts (fluid filled sacs) and fibrosis
People with CF have a genetic mutation Trusted Source in a gene called the cystic fibrosis transmembrane conductance regulator (CFTR). This gene controls the CFTR (Cystic fibrosis transmembrane conductance regulator) protein.
The protein is present in every organ trusted source that creates mucus. It is also present in other organs and tissues, including those in the: Lungs, Pancreas. Intestines, Liver, Heart, Immune system Sweat glands
SYMPTOMS OF CYSTIC FIBROSIS
Cystic Fibrosis most commonly affects the lungs, causing respiratory symptoms, such as: wheezing, Shortness of breath ,Persistent coughing which may bring up blood or mucus, Other breathing difficulties ,Trouble with bowel movements or frequent, greasy stools ,Wheezing or trouble breathing ,Frequent lung infection ( recurrent pneumonia or bronchitis ),Infertility, especially in men Trouble growing or gaining weight, Skin that tastes very salty, Recurrent sinus infections, A nagging cough.
CAUSE OF CYSTIC FIBROSIS
Cystic fibrosis is genetic. People who have CF inherit two faulty genes, one from each parent. CF is said to be recessive because you need to have two gene variants to have the condition itself. (An older name for gene variant is gene mutation.)
Your parents don’t have to have cystic fibrosis for you to have CF. In fact, many families don’t have a family history of CF. The CFTR gene contains codes for producing a protein that controls the flow of salt and water across cell membranes. In someone with CF, this gene does not function as usual, leading to low levels of salt and water outside the cells. The result is unusually thick, sticky mucus.
CYSTIC FIBROSIS COMPLICATIONS
- The lungs aren’t the only part of our body CF damages. Cystic fibrosis also affects the following organs
- Pancreas. The thick mucus caused by CF blocks ducts in your pancreas. This stops proteins that break down our food, called digestive enzymes, from reaching your intestine. As a result, our body has a hard time getting the nutrients it needs. Over time, this can also lead to diabetes.
- Liver. If the tubes that remove bile get clogged, our liver gets inflamed. This can lead to severe scarring called cirrhosis.
- Small intestine. Because it can be hard to break down high-acid foods that come from our stomach, the lining of the small intestine can wear away.
- Large intestine. The thick fluid in our stomach can make your poop large and harder to pass. This can lead to blockages. In some cases, our intestine may also start to fold in on itself like an accordion, a condition called intussusception.
- Bladder. Chronic or long-lasting coughing weakens our bladder muscles. Almost 65% of women with CF have stress incontinence. This means that you leak a little pee when you cough, sneeze, laugh, or lift something. Though it’s more common in women, men can have it, too.
- Kidneys. Some people with CF get kidney stones. These small, hard globs of minerals can cause nausea, vomiting, and pain. If you don’t treat them, you could get a kidney infection.
- Reproductive organs. Excess mucus affects fertility in men and women. Most men with CF have problems with the tubes that move sperm, called the vasa deferentia. Women with CF have very thick cervical mucus, which can make it harder for a sperm to fertilize an egg.
- Other parts of the body. CF can also lead to muscle weakness and thinning bones, or osteoporosis. Because it upsets the balance of minerals in our blood, it can also cause low blood pressure, fatigue, a fast heart rate, and a general feeling of weakness.
HOMEOPATHIC TEATMENT OF CYSTIC FIBROSIS
Homeopathy helps in getting healthy lung tissue and improvement in complaints like shortness of breath cough etc. Homeopathic treatment for cystic fibrosis helps the individual to feel better. It helps in reducing pain. Some of the homeopathic remedies for cystic fibrosis are
Thuja, Silicea, Calcarea carb, Sanguinaria can