Find support, or help research
People near you who know what living with Pompe disease is like, and ways you can help find better treatments.
Support groups in Greece
- Πανελλήνιος Σύλλογος Ασθενών και Φίλων με Λυσοσωμικά Νοσήματα «Η Αλληλεγγύη»Panhellenic association of patients with lysosomal diseases, including Fabry, Gaucher and Pompe disease; listed by FIN, IGA and IPA.All of Greece
Contact details come from each group's own page and are checked every 3 months.
Help research
You do not need to join a trial to help. Below are the programmes we found in Greece and how to reach them. You contact them yourself: Frontlight does not collect or pass on your details.
Give blood or tissue for researchResearchers use stored samples to find what causes Pompe disease.
Share your health dataA registry collects health data, without your name, so research teams can study many people at once.
Take part as a healthy volunteerStudies need people without Pompe disease to compare with. Family and friends can help.