We asked participants which changes to their practices they were planning or implementing as a result of the COVID-19 pandemic. Forty seven percent reported increased use of telemedicine, 49% limiting use of therapies, 50.4% promoting the use of home care, and 7.7% were not planning any changes. Just less than 60% (58.4%) felt they had been given enough information about COVID-19 to appropriately counsel and screen people with SCI/D; only 38.8% felt that their patients with SCI/D had been given enough information about COVID-19. When asked whether their patients with SCI/D had contacted them with concerns about COVID-19, 34.1% said they had. Specific concerns that had been relayed included increased vulnerability to infection (76.9%), fragility of caretaker supply (42%), inability to obtain necessary routine supplies (40.2%), inability to be appropriately tested (28.5%), inability to obtain transportation to health care appointments (21.3%), and inability to self-quarantine (20.7%).