Networking Lunch

Topics:

  • Transitioning from Pediatric to Adult Care
  • Shared Decision-making with Your Care Team
  • Getting Involved in Rare Disease Advocacy
  • Rare Relationships and Dating
  • Self-care for Rare Caregivers
  • Transitions out of the Home to Independent Living and College
  • Newly Diagnosed and Finding a New Normal
  • Living Undiagnosed
  • Rare Despair, Bereavement, and Anticipatory Grief
  • Rare Awareness and Connections on Social Media
  • Rare Men
  • Rare Teens and Young Adults
  • The Rare Sibling Experience
  • Parents of Newly Diagnosed Rare Pediatric Patients
  • Long-term Survivors