The MdDS Foundation, in partnership with the National Organization for Rare Disorders (NORD), has launched the MdDS Patient Registry, a study with global reach to study Mal de Débarquement Syndrome (MdDS). Let your data tell your story!
The MdDS Foundation, in partnership with the National Organization for Rare Disorders (NORD), has launched the MdDS Patient Registry, a study with global reach to study Mal de Débarquement Syndrome (MdDS). Let your data tell your story!