Cystic fibrosis therapy
What is cystic fibrosis?
Cystic fibrosis (CF), also known as mucoviscidosis, is a genetic metabolic disorder that mainly affects the airways and the digestive system. It is caused by a change in the CFTR gene, which is responsible for producing a particular protein. In people with cystic fibrosis, the function of this protein is impaired, which leads to a disrupted flow of salt and water in the cells. As a result, the airways, the gastrointestinal tract, the liver and other organs become increasingly blocked by thick mucus. Symptoms and severity can vary from person to person — common ones include a chronic cough, recurring respiratory infections, digestive problems, weight loss and delayed growth.
Our approach
For more than 25 years, our therapists have worked with cystic fibrosis patients and have built up a wealth of experience. From infancy onwards, respiratory therapy is — alongside medication — an essential part of treatment. Characteristic of the condition is the accumulated amount of thick bronchial mucus, which burdens the airways and impairs gas exchange in the lungs.
What you learn with us
With us, you will learn a range of specially developed techniques and breathing manoeuvres to loosen the secretion stuck to the bronchial walls and move it towards the mouth. From there, it can be coughed up gently using special coughing techniques. (Modified) autogenic drainage is one of the best-known techniques within respiratory therapy. Our aim is to teach you to clear your lungs of secretion on your own — this is especially important to make the inhalation of mucus-dissolving and anti-inflammatory medication more effective. In addition to active exercises such as stretching positions and breathing-relief postures, we use passive techniques such as reflexive respiratory therapy, which promote the elasticity of muscles, skin, fascia and tissue and reduce airway resistance. To strengthen and deepen exhalation, we use special breathing aids such as the VRP1 Flutter, Shaker, PEP and RC-Cornet.
Our goal
Treating cystic fibrosis involves a combination of measures to ease symptoms, fight infections and improve overall health. These include medication, supportive therapy to improve breathing, targeted physiotherapeutic exercises for lung expansion, nutritional counselling and psychosocial support for patients and their families. Alongside working directly with people of all ages, it is especially important to us to guide parents and relatives gently and thoroughly — so that you can support your child as best you can and are optimally involved in the therapy. Through our specialised approach and close collaboration, we provide more quality of life and the greatest possible independence.
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