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Membership is $25.00 per year minimum donation. Additional donations are appreciated.

Benefits of Membership include:

  • Our quarterly newsletter, NADF News

  • Ongoing communications, including important alerts

  • News on upcoming special events

  • Direct support of research impacting the lives of patients with adrenal insufficiency everywhere

To become a member, donate online today or print and complete the Membership Form, then send with your check to:

National Adrenal Diseases Foundation
3229 Greenpoint Ave, Suite 421
Long Island City, NY 11101, US
 

The National Adrenal Diseases Foundation (NADF) is a nonprofit 501(c)(3) organization, ID #11-2777036
​All donations are fully tax deductible.

Tribute donations

Make a donation in memory of someone who has died from complications from adrenal insufficiency.

Visit our tributes page

Please contact us if you would like to set up a tribute in memory of a loved one.

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A note from NADF co-president Lori Engler-Ginsburg

Many say that when a butterfly lands on you it’s supposed to be a visitation from someone who has passed from this world. Around the world, people view the butterfly as representing endurance, change, hope, and life—especially those of us who have an adrenal disease. I lost both of my parents in 2020, not to Covid-19. It was simply their time. The pandemic prevented me from traveling to be with them in their final days, to hold their hand and help them be at peace.

Months later, when I finally collected their personal belongings, one beautiful item instantly caught my attention. There, in a small black box, was a gold and turquoise butterfly pin that I had never seen before.  For sure, I never saw my mom wear it. It was as if she were leaving me with a special message, reminding me to endure, accept change and to continue to make it a better future. Did she know about the butterfly’s symbolism and what it meant to someone with Addison’s disease? She never mentioned it, but somehow, I believe she knew how much this pin would mean to me.

My parents will forever be in my thoughts, and this beautiful pin will stay close to my heart. Their legacy will live on in the remarkable work we all do at NADF, creating a better outcome for those of us with adrenal diseases through research, support, outreach, advocacy and awareness.

DONATE TO RESEARCH IN HONOR OF SANDRA AND ERNEST ENGLER