The Celiac Disease Center at Columbia University has established itself as a leader in the field, both nationally and internationally, by providing the highest quality, compassionate patient care for children and adults with celiac disease.
The University of Chicago Celiac Disease Center is an international center of excellence providing comprehensive patient and professional education, expert diagnosis and treatment for both children and adults, groundbreaking bench and clinical research, and active leadership in advocacy efforts.
The Center for Celiac Research and Treatment is dedicated to improving the quality of life for patients with celiac disease, while learning the cause of the disease and finding a cure.
The expert clinicians of the Celiac Center are launching www.CeliacNow.org, a multi-leveled nutrition website for the management of celiac disease. It’s full of concise, correct information that you need to maximize your health and well-being.
Boston Children’s Hospital’s Celiac Disease Program and Support Group helps hundreds of member families cope with celiac disease, an autoimmune disorder that leads to damage of the small intestine and requires children to follow a strict, gluten-free diet.
Children’s National is helping to improve the way pediatric celiac disease is diagnosed and treated. Working in partnership with concerned members of our community, our Celiac Disease Program brings together a team of expert physicians, nurses, nutritional consultants and professional counselors dedicated to developing a national model for detecting and treating celiac disease in children.
Nationwide Children’s Hospital’s Celiac Disease Center is dedicated to providing the best and most comprehensive care to children with celiac disease and their families.
This is an extraordinary place. There’s magic in our energy, our spaces, our people and our discoveries. There’s even magic in our motivation: our unblinking belief that we can eradicate childhood disease, so that one day, like magic, children will no longer need us.
Led by Sheila Crowe, MD, the celiac disease team at UC San Diego Health System comprises nationally recognized gastroenterologists and dietitian experts who are vastly experienced in treating individuals with celiac disease.
In Greece, as in many countries in Europe, knowledge of coeliac disease is limited and under-diagnosis of the disease remains a significant issue. Coeliac Greece established in Athens since 2008, as a patient-driven non-profit organization with main objectives to promote awareness regarding coeliac disease in Greece, build a supportive community for patients, families and…
The UCLA Celiac Disease Program is dedicated to providing high quality care for patients with celiac disease and non-celiac gluten sensitivity. The program aims to advance the medical community’s understanding of the disease through clinical expertise, education and research.
The Center for Celiac Disease provides specialized care and support for children with Celiac Disease and their families. Our care extends from diagnosis to long-term disease management, as we help your family navigate the gluten-free lifestyle.
CYE (Coeliac Youth of Europe) is an umbrella organization of European coeliac youth groups. It works within the AOECS. Spread all over Europe – the CYE representatives join each other at an annual meeting. CYE is an international forum for raising awareness, exchanging knowledge and working together for a better future! The vision of CYE…
Not every page on the website is in english. For chrome users, download the google chrome translate extension here. The Société belge de la Cœliaque – french for Coeliac Belgian Society – was founded in 1977 on the initiative of doctors, nutritionist, people with coeliac disease and parents who themselves have a child with coeliac…
AOECS stands for Association of European Coeliac Societies and it is an independent, non-profit umbrella organization of 27 coeliac associations in Europe. AOECS does not have any paid staff, it operates on voluntary basis. AOECS has a Board of directors, consisting of three elected representatives. The legal seat is situated in Brussels, Belgium. AOECS acts…
To translate the website into english, download the google chrome extension google translate. Our mission is to inform and facilitate exchange of information between people suffering of it hoping the one day we will have a support group for the Romanian patients as there are in all European countries.
The Canadian Celiac Association / L’Association canadienne de la maladie coeliaque is a volunteer-based, federally registered charitable organization with its national office in Mississauga, Ontario. It was founded in 1972 with financial assistance from the Kaufman Foundation. The association was started by two women from Kitchener, Ontario, who, from personal experience with celiac disease, recognized…
Who we are and what we do ACEA is an association that provides information to patients with celiac disease, is intolerant to gluten, a protein found in wheat, Lord, rye and oats. The Celiac Association of Andorra, nonprofit organization, was founded in 2002 by a group of parents, relatives and affected by celiac disease.Our objective…
To translate the website into english, download the google chrome extension google translate.
To translate the website into english, download the google chrome extension google translate.
People who have celiac disease often face years of misdiagnosis and difficulties with living a gluten-free lifestyle. The Adult Celiac Disease Program exists to solve those problems with accurate diagnoses and supportive treatment.
To translate the website into english, download the google chrome extension google translate. Mission Celiac Foundation Panama is a nonprofit foundation whose main objective is to raise awareness of celiac disease, the gluten-free diet, and to promote and encourage the study of celiac disease in Panama in order to improve the quality of life of all…
The Celiac Society Rajasthan is an idea of socially dedicated committed health professionals, nutrition professional and celiac patients and their families. A truly non-profit organization, incorporated on August 9th, 2010 with a message across the society:
The Coeliac Association Malta helps and supports newly diagnosed coeliacs with the aim of improving the quality of life of coeliac patients. Increases awareness amongst the catering industry, i.e. Hotels and Restaurants regarding the strict gluten free diet that a diagnosed coeliac has to follow. Activities are held quite frequently – Medical, Dietetic Speakers are…
About Us Coeliac Australia’s Vision To enhance the quality of life of people requiring a gluten free diet for life and to encourage and support research towards a cure or other ethical forms of treatment. Coeliac Australia is a national federated not-for-profit body comprising five state organisations supporting people with coeliac disease, dermatitis herpetiformis and…
We support those with coeliac disease, dermatitis herpetiformis and those on a gluten free diet. Vision: People with coeliac disease are diagnosed quickly, live healthy lives and have the prospect of a cure. Mission: Engage with Coeliac NZ members and stakeholders to support and improve the health and welfare of people with coeliac disease.
Welcome to the Czech Republic The availability and choice of gluten-free products in the Czech Republic is steadily improving. It is no more a problem to spend holidays in Prague and other bigger cities without being stressed about your diet! Our website is here to help you.
To translate the website into english, download the google chrome extension google translate. Danish Celiac Association (DCA) is an organization for people who are intolerant to gluten. The association was founded in 1979 and has approximately 2,500 members today. The association objectives: Drive celiac special interest and provide information and advisory services relating to the physical,…
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