Patients + Researchers = Better outcomes for all
Pediatric eczema is a complex disease with a growing list of treatment options. It’s also a disease that affects everyone differently and what works for one might not work for another. The patient perspective is a critical component of eczema research that fosters new understandings in treatment effectiveness and improves long-term health outcomes.
The National Eczema Association (NEA) and Pediatric Dermatology Research Alliance (PeDRA) created ECZEMA COUNTS as a shared platform to build knowledge among patients, caregivers, researchers, and clinicians. We think the more patients know about how research works, the more motivated they’ll be to share their voice. And the more researchers incorporate patients’ experience in their work, the more likely it will revolutionize eczema care.
In this series of fun and exciting games, participants will grow their knowledge and compete against one another, all toward the ultimate goal of advancing pediatric eczema care.
Sign up today to join in on the fun or continue playing for more opportunities to grow your knowledge and win cool prizes.
What is Eczema Counts?
Patients, caregivers, and researchers competing against each other, all toward the ultimate goal of advancing pediatric eczema care
Prizes awarded to participants who climbed to the top of the leaderboards as they learned more about the value of PCOR in childhood eczema
Shared vision of alleviating the burdens of pediatric eczema by growing knowledge and building bridges to guide the best possible treatment decisions