Scholarships Available for Milan Meeting

Congenital Hyperinsulinism International is thrilled to announce family scholarship grants for the upcoming CHI Family Conference in Milan on September 17 and 18, 2013.  The Family Scholarships will cover the cost of registration for two family members and one night at the conference hotel, the NH Milano 2 Hotel.  This generous donation was provided by … Read more

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SAVE THE DATE: HI FAMILY CONFERENCE MARCH 17-18, 2012

SAVE THE DATE Congenital Hyperinsulinism Family Conference March 17-18, 2012 Philadelphia, Pennsylvania Congenital Hyperinsulinism International (CHI), in conjunction with the Children’s Hospital of Philadelphia (CHOP), invites you to attend the fourth Congenital Hyperinsulinism Family Conference. Conference attendees will learn about recent advances in the diagnosis and treatment of congenital hyperinsulinism (HI) from experts in the … Read more

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Endocrine Society Dinner Meeting

Please join us for the Congenital Hyperinsulinism International (CHI) Endocrine Society Dinner Meeting on June 4, 2011 from 6:30-9:30 PM at the Seaport Hotel in Boston, Massachusetts. Dinner meeting participants will have an opportunity to speak informally on a range of topics with members of the CHI Scientific Advisory Group comprised of leading world specialists … Read more

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A WOW Conference: The Genetic Diseases of Children

Have you ever gone to an event where you were so excited about meeting every last person that even waiting on the Ladies Room line was a chance to meet fascinating people? The Genetic Diseases of Children Conference, which is taking place in New York right now, is just such an event. Yesterday, I had … Read more

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Canadian Organization for Rare Disorders 2010

Isabel Calderón, a member of the CHI Board of Directors from Canada, attended the Annual Congress of the Canadian Organization for Rare Disorders (CORD) held in Ottawa on October 1-2, 2010.  A full two days of presentations and workshops made up the agenda.  About 120 representatives from different Canadian rare disorder associations and individual patients … Read more

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