
National Foundation For Ectodermal Dysplasias
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- The NFED is the worldwide expert on ectodermal dysplasias and the only advocacy organization in the U.S. dedicated to individuals living with these disorders. Our mission is to empower and connect people touched by ectodermal dysplasias through education, support and research.In 1981, Mary Kaye Richter and 12 other families affected by ectodermal dysplasias organized and founded the NFED. The NFED has grown considerably since the early 1980s, a time when little was known about the rare conditions and the medical literature cited only a half dozen affected individuals in the United States. Today, we serve more than 5,100 families worldwide. When you are missing some or all of your teeth, smiling, eating and talking are not easy. The NFED believes every person deserves a smile. We work with families to help them understand their treatment choices, to increase their access to care and to find financial assistance for that care. We have a network of 20 Dental Treatment Centers, educate care providers, and have provided clients with more than $1.5 million in assistance for care.We have funded more than $2.5 million in research at 40+ centers around the world and sponsored numerous scientific conferences for specific syndromes and classification. NFED-funded research projects have identified genes for numerous ectodermal dysplasias, established treatment protocols and characterized many of the syndromes. Perhaps our greatest success comes from providing individuals and families affected by ectodermal dysplasia with a place to turn for reliable information, support and hope. We publish quality information to empower families with knowledge that their doctors often cannot give. We stand with open arms to welcome the family who has just been diagnosed, to answer their questions, and to allay their fears. The conditions come with challenges, but with support and encouragement, families can expect a bright future.
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Headquarters:6 Executive Drive Suite 2, Fairview Heights, Illinois, United States
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Phone Number: +1 618-566-2020
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Website: https://www.nfed.org
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Employees:13
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Revenue:$1 - 10M
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Legal Name:National Foundation For Ectodermal Dysplasias
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| NAICS Code: 0 |
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Frequently Asked Questions regarding National Foundation For Ectodermal Dysplasias
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Where are National Foundation For Ectodermal Dysplasias's Headquarters?
National Foundation For Ectodermal Dysplasias's Headquarters are in 6 Executive Drive Suite 2,Fairview Heights,Illinois,United States
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What is National Foundation For Ectodermal Dysplasias's phone number?
National Foundation For Ectodermal Dysplasias's phone number is +1 618-566-2020
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What is National Foundation For Ectodermal Dysplasias's official website?
National Foundation For Ectodermal Dysplasias's official website is https://www.nfed.org
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What is National Foundation For Ectodermal Dysplasias's Revenue?
National Foundation For Ectodermal Dysplasias's revenue is $1 - 10M
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How many employees are working in National Foundation For Ectodermal Dysplasias
National Foundation For Ectodermal Dysplasias has 13 employees
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What is National Foundation For Ectodermal Dysplasias's Industry?
National Foundation For Ectodermal Dysplasias is in the industry of Non-Profit Organization Management
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Who is National Foundation For Ectodermal Dysplasias's Founder And Chairperson, Rally For Ally?
National Foundation For Ectodermal Dysplasias's Founder And Chairperson, Rally For Ally is Ashli George
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Who is National Foundation For Ectodermal Dysplasias's Director Of Administration?
National Foundation For Ectodermal Dysplasias's Director Of Administration is Gale Hoedebeck