The World Duchenne Organization and several of its members have been advocating for better use of Duchenne data, which is currently kept in silo’s. WDO does this by bringing this subject to the attention of the EU lobby, by developing tools enabling better data sharing, such as the Duchenne Data Platform, and organizing meetings on how to enhance data sharing for Duchenne.
Engaged patients and their family members feel a dire need for much more effective (re)use of their data, as well as their own time and skills in knowledge discovery and the fast-track translation of knowledge derived from studies into health practice.
There is general agreement that the data collected from a person ‘belongs’ to that person in the sense that reuse of the data for other proposes than for which the original consent was given (if any) lies with that person. In the EU this is now also regulated by the GDPR (General Data Protection Regulation). Medical professionals and researchers are increasingly obliged to provide the data to the person from which they originated upon request, but in actual practice it is still a very cumbersome and discouraging process for individual patients to ‘recover’ their data from medical and research collections spread over many different places.
World Duchenne Organization on March 21 and 22, 2019 organized a meeting in Amsterdam to discuss the FAIR initiative, the Personal Health Train, Duchenne Data Platform and next steps related to data visiting. The meeting was attended by representatives of registries, patient advocate leaders, clinicians, scientists, companies and regulators. A Data Declaration resulted from this meeting. A workshop report is published in Neuromuscular Disorders (Official journal of the World Muscle Society). If you want to receive a copy please send a message to:
Please read, share and sign our Data Declaration: