CF impacts the cells in the body that make sweat, digestive fluids and mucus. Normalmente, these are very slippery and then systems that keep the body working smoothly. Contudo, if you have CF, they become thick and glue. Causing these funds to black tubes and ducts within the body.
People with CF have chronic and persistent lung infections that make it difficult to breathe over time.
Ao longo do tempo, mucus accumulates inside your airways; This makes breathing a struggle. The mucous traps germs and leads to infection. IT can also cause severe lung damage like a cyst (fluid-filled sacs) and fibrosis (scar tissue). That is how CF got its name.
Symptoms of CF
People with CF have several symptoms, Including;
- Very Salty -tasting skin
- Non-stop coughing, at times generating phlegm
- Frequent lung infections including bronchitis and pneumonia
- Poor growth or weight gain in spite of a healthy appetite
- Wheezing or shortness of breath
- Frequent greasy, or bulky stools, difficulty with bowel movement
- Male infertility
What Causes Cystic Fibrosis?
It is not contagious; It is produced by a deviation (change) within a single gene described as the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR,) This controls the flow of salt and fluids in and out of your cells. If the CFTR gene does not work as it should, glutinous mucus mounts up throughout your body.
To get CF, you have to receive a mutated copy of the gene from both your parents.
If you only inherit one copy, you will not exhibit any symptoms, But you will be a carrier for the disease. That indicates there’s a possibility you could pass it on to your child one day.
Sobre 10 million Americans are CF carriers. Every time two CF carriers have a baby, existe um 25% (1 e 4) chance that their baby will be born with Cystic Fibrosis. There is a 50% chance the child will be a carrier but not have CF. There is a 25% chance that the child will not carrier CF gene or have CF.
Which Portions of the body does CF affect?
The lung is not the only part of the body that is affected by CF. CF also impacts the Liver, pâncreas, small intestines, large intestine,
and kidneys, Bexiga e Reprodutivos órgãos.
As pessoas com fibrose cística têm o maior risco de infecção pulmão em desenvolvimento por causa do muco pegajoso construir, cria um ambiente em que os germes podem prosperar e crescer. infecções pulmonares são causadas principalmente por bactérias e tendem a ser um problema muito sério.
- Fígado: Se os tubos que a bile de transporte tornam-se conectado, seu fígado se inflamam, e cicatrizes graves ou cirrose ocorre.
- pâncreas: O muco espesso causada por intermédio de condutas de bloco CF no pâncreas. Isso interrompe enzimas digestivas (proteínas que quebram sua comida) de alcançar seu intestino; como um resultado, seu corpo tem um tempo difícil absorver os nutrientes de que necessita. Com o tempo isso também pode levar a diabetes.
Intestino delgado- Desde quebrar alimentos ricos em ácidos que vêm do estômago é difícil, a mucosa do intestino delgado pode começar a corroer.
- Intestino grosso: Thincscreations (líquidos) no estômago pode fazer fezes muito grossa. Isso pode provocar bloqueios, Em alguns casos, o intestino pode também começar a dobrar sobre si mesma como um acordeão em desordem chamada intussuscepção.
- Bexiga: Chronic coughing weakens the bladder muscles, Almost 65 of omen with CF suffer from stress incontinence” This means that you leak urine when you sneeze, tosse, laugh or try to lift something, Although this is more common in women, it can occur in men.
- Rins: Some people with CF get kidneys stones. These small, hard mineral deposits can generate nausea, vómitos, e dor. If ignored, they can lead to a kidney infection.
- Reproductive organs: surplus mucus affects fertility in both men and women. Most men with CF have problems with the tubes that transport their sperm, or what;s called the vasa differentia. Women with CF have very thick cervical mucus, which can make it harder for sperm to fertilize an egg.
- Other parts of the body: Cystic Fibrosis can also lead to thinning of the bones or osteoporosis ) e fraqueza muscular. Since CF upsets the balance of minerals in the blood, it can also produce lower blood pressure, fadiga, a fast heart rate and overall feeling of weakness.
Treatments for Cystic Fibrosis:
The type of severity of CF symptoms can differ based on the person. So it’s important to have a treatment plan that contains elements that are unique to each’s situation.
People with CG should work closely with their medical providers and families to create personalized treatment plans.
Look to the CF Foundation, which accredits more than 120 care centers that are staffed by dedicated experts in CF to help care for patients through specialized disease management.
Each day, pessoas com FC têm tipicamente uma combinação das seguintes terapias:
- desobstrução das vias aéreas para ajudar a soltar e limpar o muco espesso que podem se acumular nos pulmões, Algumas técnicas de desobstrução das vias aéreas pode exigir alguma ajuda da família, amigos ou terapeuta respiratório. Muitas pessoas com FC utilizar um colete inflável que é usado no peito e vibra em um pulso de alta para ajudar a soltar e muco fino.
- medicamentos inalados para abrir as vias aéreas ou diluir o muco. These are liquid drugs that are made into a mist or aerosol and the inhaled through a nebulizing. Tese medicines include antibiotics to fight lung infection and therapies to help the airways clear.
- Pancreatic enzyme supplement capsule to help improve the absorption of vital nutrients. These supplements are taken with every meal and most snacks. People with CF will usually take multivitamins.
Although CF is a serious condition that requires daily care, many treatments for it have advanced. People who have CF live much longer than they use to and the quality of life have improved too.