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Search Results for “the advocate”

How Dietary Supplements Helped My Eczema from the NEA Community

Five members of the NEA community share their stories of how they used supplements to improve their eczema symptoms.

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Bullying and Self-Esteem in Kids with Eczema

Many studies have looked at how teasing and bullying based on appearance affects people physically and mentally.

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My Skin Talks To Me: My Experience Living With Eczema for 40 Years

In my 40-plus years of living with eczema, I’ve learned that my attitude profoundly affects how my disease responds to treatment.

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Eczema Boot Camp: Suzanne’s Story

The Eczema Boot Camp regimen perhaps did not save my life, but it gave me back my life. Wet wrap therapy is the most effective tool I’ve found after 36 years of struggle.

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Father of the Year

A competition at his gym enabled Anthony Trias and his teammates to win a $5,000 prize, which was donated to NEA in honor of his son, Aiden.

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Coalition United for Better Eczema Care (CUBE-C)

As part of its mission to improve the health and quality of life for individuals with eczema through research, support and education, the National Eczema Association (NEA) advocates for better medical care. Current eczema care is often fractured, uncoordinated, and many practitioners have not yet been informed about the best treatment protocols and emerging eczema […]

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October 2018 declared Eczema Awareness Month in Georgia!

As part of NEA’s Raise Your Voice campaign, eczema advocates are working with state legislators to raise eczema awareness.

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How new federal policies could impact eczema health care

NEA’s vice president of advocacy and access explains how today’s political climate might affect insurance coverage and treatment options for people with eczema.

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Living well with eczema (and all the ways to do it)

We asked a patient, medical doctor and psychologist for their best advice to conquer the daily struggles of life with atopic dermatitis.

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Hungry for eczema relief? You’re not alone.

Culinary expert, author and TV personality Elizabeth Falkner is living with AD and wants to help get the word out.

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