For those who are recently diagnosed, we offer support and information in a variety of ways. If you attend our PD101 session which takes place annually, you will get lots of information from a qualified doctor. But your doctor does not know what it is like to live with Parkinson disease, so we follow up with P2P—an opportunity to hear from several PWPs (Persons with Parkinson's) who will share their stories and answer your questions. It's offered a few weeks after PD101.