Created for individuals and families managing food allergies, the FARE Patient Registry harnesses the power of patient data to accelerate research toward revealing the causes of food allergy, uncovering why food allergy rates have increased in recent years and identifying which treatments might be most effective for individual food allergy patients.
The registry will serve as a data bank to collect demographic and clinical information on all patients, including clinical histories, lab reports and eventually bio-specimens (serum, DNA and RNA) and make this information available to the greater medical community. Demographic information can better define the real-world food allergy population and enhance the understanding of the natural course of the disease. This knowledge can be used to develop evidence-based guidelines for diagnosing and monitoring patients.
The domain of food allergy research has many unanswered questions, and your health information will help us get the answers. FARE will use the anonymous data to organize and analyze participants' real-world experiences to prioritize and answer the important research questions. A patient registry is the single most important development our community can do that will further our understanding of food allergy and lead the way for the discovery of novel treatments and a potential cure.
- Advance the scientific understanding of food allergies
- Create a personal repository of patient data to study how accidental exposures and reactions occur
- Examine and standardize care for those living with food allergies
- Develop better ways to diagnose food allergy
- Improve and develop guideline-recommended treatments for food allergies
- Promote awareness and understanding of food allergies
- Understand the causes of food allergy (including anaphylaxis) and find new ways to prevent it
Some Topics We Are Investigating
- Improved food labeling
- Treatment of food-induced anaphylaxis
- Treatments that cure food allergy or lessen the severity
- Factors that help patients better manage their food allergy
- Genetic screening to define risk of food allergy
- Diagnostic testing, predictors and biomarkers for food allergy and anaphylaxis
- Genetic and environmental contributions to the development of food allergy
- Psychosocial impact and mental/behavioral health
- Best practices guidelines for assessing and treating psychosocial disorders
FARE Has the Network
Collecting clinical data from patients with food allergies can transform food allergy research because this has not been done before. With this goal in mind, we created the FARE Clinical Network. This collaboration among the nation’s top research and clinical care centers distinguishes the FARE Patient Registry from all other registries. In 2015, FARE invested in the FARE Clinical Network – and now funds more than two dozen sites across the country – for the dual purpose of elevating the level of patient care and accelerating research to improve the lives of millions affected by food allergies. FCN members have agreed to provide data to the FARE Patient Registry, and we plan to mine this data to build a robust and comprehensive patient database.
When you register you will be asked questions about your or your children’s personal experiences as a food allergy patient. This information will be used to learn how food allergies affect individuals and families and encourage the creation of clinical trials with the goal to get us all closer to new treatments.
We are looking for individuals of all ages with diagnosed food allergy. Signing up to the FARE Patient Registry is an important step that will provide critically important data to assist research in a number of ways and help individuals track their own disease. The registry will empower patients through a personalized patient portal, to share health information and make contributions that connects patients, clinicians, researchers, biopharma therapeutics developers and advocacy organizations.
Here is how you can contribute
Joining the registry takes commitment but making a difference is simple and easy. How will you contribute?
Consent. Patients will be asked to read and sign a consent or assent form agreeing to participate.
Answer surveys. As a participant, you will answer questions about your personal experiences as a food allergy patient from your computer or smart phone. We promise you won’t have to be active all the time.
Share medical records. Participants can upload physician notes and test results to provide information about confirmation of diagnosis
Tell us when you have a reaction. It’s critical for researchers to know why you have an accidental exposure and when you visit the ER for treatment.
Participate in clinical studies. The only way to develop new therapeutics is to learn what works for patients like you
Stay in touch. We hope you participate in the registry for many years and enjoy the benefits that sharing data can bring. It is the only way we will know who gets better and why. Your commitment is only 15-20 minutes every 4 months and can be spread over time.
How will I learn about clinical trials?
The FARE Patient Registry will also serve as a recruitment database that can be used to address the difficulty in enrolling patient into clinical trials and connect you with leading researchers and scientists.
The process of recruiting patients is challenging and can often take a long period of time. If researchers cannot find enough patients to join a study, this can often delay discoveries that can benefit the food allergy community at large. Your participation in this registry and potentially, clinical trials, could help the community accelerate that process considerably. Researchers will never contact you directly. The FARE registry coordinator will contact you with information about a study or clinical trial by email.