Research Fund Established for Congenital Hyperinsulinism Research

A research seed money fund in the amount of $50,000 has been established at NORD for the study of congenital hyperinsulinism (HI). The fund provides $25,000 for two years for a scientific, pre-clinical research study related to the diagnosis and/or treatment of congenital hyperinsulinism in neonates or children. The deadline for submission is May 4, … Read more

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HI Tweens and Teens Have an Opportunity to Give Back

During the Fourth Congenital Hyperinsulinism Family Conference to take place March 17th and 18th at the Children’s Hospital of Philadelphia (CHOP), tweens and teens with HI and their siblings will produce a show that will be broadcast to pediatric patients at CHOP. A gift from the Ryan Seacrest Foundation for a recording studio known as … Read more

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A Rare Disease Day Well Celebrated

If you had one extra day in a given year, how would you spend it? Last week there was just such a day, and along with 110 other people I attended a fantastic party: the Congenital Hyperinsulinism International (CHI) Very Special Cocktail Party in Glen Ridge, New Jersey. Yes, the day I’m talking about is … Read more

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Focus on Advocacy

CHI is presenting a series of blog articles on the speakers who will be addressing families attending the Fourth Congenital Hyperinsulinism Family Conference March 17 and 18, 2012, in Philadelphia, PA. In this article, we focus on advocacy issues and present Mary Dunkle, Melanie Cohen, and Kristin Crossland. Advocacy is one of the most important … Read more

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