No.
We believe synthesized data on the lived experience of these conditions is the key to truly understanding them and guiding clinicians, researchers, and industry toward work that improves our quality of life and health outcomes. The more information we can provide as a group, the higher quality that data will be. It is your choice whether you want to include your data in this effort.
During the current Beta phase, no data recorded will be used for research. You will be asked to reconsent or opt out of sharing data when this changes.