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We offer a few ways you can share love with NEA and the eczema community this Valentine’s Day.
Seasoned NEA advocates Cara Ellis and Amber Jewett offer their advice for effectively communicating with elected officials.
Every year, eczema warriors gather on Capitol Hill to share their stories with legislators, pushing to fund national research and improve access to eczema treatments. Join NEA’s grassroots movement and learn how to speak with Members of Congress about the issues that matter to you.
Thank you to our 2019 IFAC participants who helped us raise more than $8,000 for eczema research, resources and support. We couldn’t have done it without you.
Researchers are starting to identify distinct characteristics of atopic dermatitis in elderly patients along with special considerations required for diagnosing and treating them.
As the mother of a 6-year-old with eczema, life without the National Eczema Association is not a life I want to know.
NEA is ramping up its efforts at the state and federal levels to end step therapy, the health insurance protocol that requires patients to try and fail other medications before approving coverage for the treatment originally prescribed by their doctor. Want in on the action? All it takes is a quick phone call.
NEA has come a long way since its inception in 1988, thanks to three dedicated people in Portland, Oregon, who watched their small grassroots nonprofit evolve into the global eczema community it is today.
Eczema warrior Kuniko Nakamura shares her journey through yoga, mindfulness awareness practice and meditation.
Eczema warrior Ryland Mortlock shares his experience meeting with Congress members at Capitol Hill to help boost federal funding for medical research.