Patient Advocacy – Individual event: Would you benefit from communicating with a person like you who has Dry Eye Disease (DED)? A person with DED who has “been there and done that” as the saying goes. Someone who probably will be able to help you to become a better educated consumer in dealing with your DED. You will be able to communicate individually by emails or even talk by phone, Skype or Zoom to ask your questions and get feedback and options that are likely to be helpful to you. Of course it is free. You can connect with a Patient Advocate by completing the request form now.
Coming in the future:
Ask a Doctor will be a live audio webcast that provides answers to your questions about Dry Eye, co-morbidities, symptoms, and their treatments.
The event is hosted periodically by Not A Dry Eye Foundation. An ophthalmologist or optometrist will discuss an aspect of the disease and answer your questions.
Patient Support Groups are for adults who struggle to understand their Dry Eye symptoms. Patients can connect with other patients, learn more about their symptoms, and support each other through their shared experience.