HypoCare by CHI

Reliable HI information, family support, and research updates, all in one place.

Congenital Hyperinsulinism International (CHI) is a global nonprofit organization dedicated to improving the lives of people affected by congenital hyperinsulinism (HI). CHI created HypoCare to provide access to trusted resources, research opportunities, educational materials, and community support. HypoCare is designed for individuals living with HI, caregivers, healthcare providers, and researchers.

Key features of this app include: Research participation. Join the HI Global Registry (HIGR) to share your HI experience to advance HI research. Educational resources. Learn about HI, including diagnosis, genetics, treatment, and management strategies. Treatment information: A simplified version of the published International HI Care Guidelines are available to help clinicians and families understand agreed upon expert advice related to HI management. Family and caregiver support. Access content for newly diagnosed families, including a glossary of HI terms, adjusting to the diagnosis, how to find community support, and more. Community and Advocacy: Find ways to engage with the HI community, learn about advocacy efforts, and stay updated on CHI news and events.

The content on this app, including text, graphics, images, and other material, is provided for informational purposes only and does not constitute professional medical advice, diagnosis, or treatment. The information on this app is not a substitute for medical treatment by a qualified health care provider. Always seek the advice of your physician or other qualified healthcare provider with any questions you may have regarding a medical condition. In the event of a medical emergency, you should immediately seek care at a hospital emergency department or call an emergency ambulance service. Never disregard professional medical advice or delay seeking professional medical treatment because of something you have read on this app.