In Reply The enthusiasm expressed for the Million Brains Initiative 1 and the thoughtful consideration of ethical facets by Byram and Illes are much appreciated. The authors underscore a few of the inevitable ramifications that will undoubtedly parallel the realization of precision stroke medicine and the transformation from blissful ignorance to big data in stroke medicine. 2 The current paradigm for cerebrovascular disorders from stroke to dementia is founded on individual clinical symptoms that prompt the acquisition, routine interpretation, and archiving of neuroimaging results. Impressions are readily generated and documented in the electronic health record of every individual. Such imaging data are unnecessarily isolated, antithetically preventing the use of the big data approaches that are required to define the incidentaloma, or 1-in-a-million concept. 3 Similarly, normative changes in the brain across the age span and the construct of cerebrovascular health are only achievable by disrupting this archaic and disconnected health care framework. 4 Crowdsourcing such data will likely unfold like the methods enveloping all aspects of life in the postdigital age, with empowered patients rapidly gaining and reclaiming access as the owners of their health care data.The nidus for the formative concept and definition of cerebrovascular health resides with using imaging through the Million Brains Initiative as an initial step along the research trajectory required to directly address the ethical challenges raised by Byram and Illes. Crowdsourcing the Million Brains Initiative does not replace the existing clinical paradigm and chain of responsibility in routine clinical care. Moreover, these big data and related research findings on potential incidentalomas are required to define any imaging finding as incidental. Potential crowdsources for gathering imaging results for a million brains include patients not providing new scans, but rather those that have already been interpreted and billed; thus, any responsibility for incidental findings belongs to the interpreting physician. A second crowdsource is the vast number of already completed clinical research studies, of both small and large sample size, that pooled represent a substantial data set on which to make large and important observations. 5 Again, this source of imaging has already been obtained and reviewed for any incidental findings by the study principal investigators. Thus, the "discovery" of anomalies in the Million Brains Initiative would be very close to zero and should not be viewed as an impediment to putting such a powerful initiative to work.The argument of the authors regarding distributive justice is a major concern in all areas of biomedical research while the observations about cerebrovascular health that the Million Brains Initiative might generate-the true incidence of silent stroke, an improved understanding of age-related cerebral atrophy, or the anticipation of a tailored therapy for a specific group-are more likely to be tangibly acces...