Get ideas, words of encouragement, and tips from people like you who are living with PAP. Everybody has a personal story to tell. You can find some of them here.
When Moritz was only 6 years old, his mother was diagnosed with PAP. He does not remember her getting the actual diagnosis, but he recalls the sudden change in his family’s everyday life and that he often felt sad.
Married and the mother of two. A quite normal situation for a woman in her 30s. But Jacqui is living with a disease far from normal – pulmonary alveolar proteinosis (PAP). And it reared its ugly head at the worst time possible.
You wouldn’t think that Paul had any kind of illness. He is the father of three; he works full time and plays golf in his spare time. When diagnosed with pulmonary alveolar proteinosis (PAP) Paul’s main focus was to get on with his life and work – and after some time he did.
Julie looks like any 15-year old girl. She attends school, goes out with her friends and is in to musical theatre. But in spite of her young age, Julie has been hospitalized several times and gone through five lung lavages after being diagnosed with pulmonary alveolar proteinosis (PAP).
When Elisabeth’s daughter, Julie, was diagnosed with pulmonary alveolar proteinosis (PAP) at the age of 11 it turned Elisabeth’s life upside down. Four years and five lung lavages later Elisabeth is happy to say that Julie is feeling better than ever.
Chronic diseases do not only affect the person with the diagnosis. Everybody around the diagnosed person is affected to some extent.
Lung diseases are among the most common medical conditions in the world. Tens of millions of people suffer from lung disease.
We aim to gather information about PAP in one place for the convenience of PAP patients and their relatives worldwide.
You can find information about PAP elsewhere on the internet. Click to know more.
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