As a cystic fibrosis patient, exchanging ideas with other sufferers can be especially important. Parents whose children have cystic fibrosis can draw hope and courage from this exchange. Day-to-day experiences of others with the disease not uncommonly open up new ways of shaping your own lives. This allows patients and family to help each other.
We have compiled some addresses of specific organisations and self-help groups that deal with cystic fibrosis for patients and family members. Here you can find sport tips, valuable information and helpful ideas on how to better manage your disease.
Muko e.V.
www.muko.info
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