F.E.A.S.T.

Families Empowered and Supporting Treatment of Eating Disorders

F.E.A.S.T.

Leadership and Advisors

Founding Principles

FEAST blog

Exec. Director's calendar

Donations

Join F.E.A.S.T.

Volunteer for FEAST

Contact FEAST

Press room

FEAST History

Our Services

AroundTheDinnerTable.org

FEAST recipe book

Specialist Directory

Media Outreach Project

Position Statements

Book reviews by parents

F.E.A.S.T. Research blog

Podcast series

Glossary of ED vocabulary

Printable info/brochures

Online Caregivers Forum

F.A.Q.s

Understanding EDs

The Family's Role

Treating Eating Disorders

Cause of EDs

Defining Recovery

Video and articles

Maudsley Approach

Find treatment providers

Online provider list

Clinical trials

Insurance & money issues

Clinical guidelines

Our stories and letters

Parent stories

Patients speak

Clinician letters

Events & conferences

ED groups worldwide

Parent Support Group List

Search this website

History of F.E.A.S.T.

In early 2008, a group of parent activists held an international phone meeting to plan the creation of the first worldwide organization to focus on parents and carers of eating disorder patients. We chose the name Families Empowered and Supporting Treatment of Eating Disorders both for its meaning as a title and for the energy and joy of its acronym. We came together after years of networking between various activists online and in person, most of us participants on an online forum that had been supporting parents since 2004 under a series of names and addresses. What we had in common was an interest in supporting patients in an evidence-based and family-based way. We shared an interest in the power of families to act assertively and work with excellent specialized treatment professionals in a team approach.

The history of eating disorder treatment has often been one of family separation and even blame, and F.E.A.S.T. created a set of founding principles to set us apart from that history and embrace newer science and practice. We invited leading clinicians and researchers and activists in the field to serve as our advisors and mentors in the same spirit of collaboration that we feel parents can achieve with the treatment professionals treating their loved ones.

In April of 2009, our organization successfully achieved 501(c)(3) nonprofit status from the U.S. I.R.S., a designation that is recognized internationally as an indication of legitimate management and practice. We have also registered our name with the U.S. Trademark Office, and we are incorporated as a non-stock organization in the Commonwealth of Virginia, U.S. Our Board of Directors and Advisory Panel live and work in several countries and we publish materials in English, Spanish, and French.

Since we began, F.E.A.S.T. has established a budget and Strategic Plan as well as a number of services. Our all-volunteer staff participates in conferences and activities around the world, and provide support to families online, by phone, and in person. Laura Collins, our Executive Director, is an active participant in the eating disorder community, speaking at conferences and writing articles for both ED and mainstream media.

In 2008 and 2009, we have been exhibitors at the National Eating Disorders Association annual conferences and plan to do so in 2010 as well. We also hold a pre-conference social event for our members and advisors to meet and network. Our conference reports are available on our website: 2008, 2009.

F.E.A.S.T. also takes a stand on issues of special importance to the parent community. In 2009 we spoke out against "Parentectomy" during hospitalization, we made a strong statement on whether parents cause eating disorders, and we voted to support an Eating Disorders Coalition talking points document on School BMI Screenings. Our Media Outreach committee has successfully worked behind the scenes to get outdated and damaging information about eating disorders changed on major websites, and we have worked with numerous news media organizations to publish science-based information on eating disorders.

Other online services, like our Recipe Book, live forum, treatment provider list, and Glossary, are available at all hours of the day for families seeking information and support.

Among our goals as an organization are: to make sure families have access to science-based information and support services as easily and quickly as possible after diagnosis, to influence eating disorder organizations and professionals to consider family as a resource, to improve public perception and understanding of eating disorders.

We are a membership organization and supported exclusively by individual donations. Please join F.E.A.S.T. and consider making a donation to help us do our work!
(Page last updated April 13, 2010)

  • 2010 EDIC conference report
  • 2009 NEDA conference in Minneapolis
  • 2009 NEDAW event in Virginia
  • F.E.A.S.T. awarded 501(c)(3) status
  • 2008 NEDA conference in Austin


F.E.A.S.T. 
(Families Empowered And Supporting Treatment of Eating Disorders)

P.O. Box 331  ♦ Warrenton, VA 20188  ♦  USA  ♦   (540) 227-8518  ♦  info@FEAST-ED.org 
 F.E.A.S.T. is registered as a nonprofit organization under section 501(c)(3) of the United States Internal Revenue Code
Information on this site is meant to support, not replace, professional consultation. Unless otherwise noted, content is edited by F.E.A.S.T. volunteers with assistance from our Professional Advisory Panel.

©  F.E.A.S.T.  2008,2009,2010 

This website is certified by Health On the Net Foundation. Click to verify. This site complies with the HONcode standard for trustworthy health information:
verify here.