We recommend data collection via one of the participating COVID19 MS data collections (list for people with MS, list for clinicians). Data sharing via registries and cohorts support short-term as well as long term research. Data entry usually takes between 5 and 20 minutes. A Fast Data Entry Track is provided and takes up to 5 minutes (submit data via the buttons below). The Fast Data Entry track contributes only to short term research.
Important note: Do not contribute data via more than one initiative