The genetic disorder alpha-1 antitrypsin deficiency is currently incurable, although numerous researchers are intensively studying gene therapy. Similarly, damaged lung tissue cannot regenerate. Nevertheless, appropriate therapy can improve your condition in several ways:
- slow the progression of the disease and thereby improve the prognosis.
- to enable an improvement in quality of life through symptom relief
The specific treatment is carried out
- by taking bronchodilating medications (anticholinergics, beta-II agonists) to relieve shortness of breath
- Under certain conditions, the missing protective protein alpha-1-antitrypsin can be administered via infusion. This so-called replacement or substitution therapy can slow the destruction of lung tissue. The alpha-1-antitrypsin is derived from the blood of healthy donors.
You will learn how the protein alpha-1-antitrypsin is normally produced in the body. here
Every treatment is based on two important pillars:
- their willingness to cooperate (Compliance)
- competent medical care, so that you feel well looked after and taken seriously
Are you lacking medical support in your region? You can find a search function for pulmonary specialists in Germany here. here Or feel free to contact us directly.




