Cystic Fibrosis bear on to an inherited aesculapian condition characterized by damage to the cells that produces mucous . This condition affects primarily the lungs , digestive organisation , and other full of life electric organ of the body . Individuals with Cystic Fibrosis inherit a defective gene which make the mucose , which is usually a slight slippery liquid state , thick such that it starts obstructing ducts and arterial blood vessel , especially in the lungs .
People with Cystic Fibrosis can be quite disabled as they do not have normal functioning vital organs of the trunk , particularly the lungs . The medical prognosis for individuals with Cystic Fibrosis is rather poor .
However , with improvements in treatments and continuous research people have much improved tone of life , can be gainfully employed , and can live a much long life than before .
Can Cystic Fibrosis be Cured?
As of now , there is no cure for Cystic Fibrosis . Treatment is aimed at calm down the symptoms and foreclose any complications that can go up due to this disease . soul with Cystic Fibrosis want quotidian care and close monitoring . The sooner the disease is diagnosed the better the quality of life of the patient becomes .
A affected role with Cystic Fibrosis will require a multidisciplinary approach towards treatment . The primary goals of intervention for Cystic Fibrosis include preventing accumulation of mucose in the lungs , controlling infections specially in the lung , and transfer any blockages that may be present in the gut due to thick mucus . Adequate sustenance is compulsory for patients with Cystic Fibrosis .
Medications in the signifier of antibiotics are throw for lung or intestinal infection which are quite frequent in mass with Cystic Fibrosis . Antiinflammatories are prescribed to quiet down the puffiness of the airways which is also quite common in people with Cystic Fibrosis .
Medications used for take down the heaviness of the mucous are give such that the patient is able to cough out excess mucous and improve functionality of the lung . Bronchodilators are also quite often given to patients to keep the airline business open .
pulmonic renewal is also advocate for patients with Cystic Fibrosis . This is a farseeing full term process and require pot of patience from the patient and the health care provider . pulmonic renewal take physical exercises to strengthen the lungs . This demand breathing exercises to ameliorate respiration .
Nutritional counseling is done where a dieting chart is ready that good suits the patient role and improves the quality of the life-time of the patient . Periodic psychologic counseling is afford to the patient and mob to help cope up with the disease shape .
There are also certain operative procedures that form a part of the treatment plan for people with Cystic Fibrosis . These procedure include adenoidal polypus removal for improved ventilation and oxygen therapy to improve O story in the body . Mucous build up in the lungs or the digestive system is suctioned out through tubes .
In the end stages of the disease , the patient role command feeding thermionic valve for nutritionary reinforcement . Lung transplant is another function that is an option reserved for patients who have severe complications of the lungs due to Cystic Fibrosis . Lung graft may be passably effective but the complications of Cystic Fibrosis always be given to retrovert even after a successful transplant .
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