The New York City Hemophilia Chapter has moved into a brand new office in the heart of Midtown Manhattan. No, it’s not actually in Times Square – but it’s very […]
This Summer, the National Hemophilia Foundation will again be hosting educational summits for families and individuals affected by hemophilia with an inhibitor. An inhibitor is an immune response [...]
As summer approaches, many young people are making plans to head to camp, Bleeding disorders camps offer unique opportunities for youth in our community to have fun, make new friends, […]
April 17 is World Hemophilia Day. This annual observance presents an opportunity to remember that although knowledge and treatment have improved greatly, high quality care is not available [...]
The February 29th edition of the Long Island Herald has a story highlighting the annual benefit dinner hosted by the Ambrosio Family in support of the New York City Hemophilia […]
NYCHC is Calling All Former Team Captains, Future Team Captains, Sponsors and Anyone Who Wants to Help Make the 2012 Hemophilia Walk Our Best Ever! Please join us for a […]
Washington Days, NHF’s annual grassroots advocacy day on Capitol Hill, will take place from Wednesday, March 7 until Friday, March 9th, 2012. This is your opportunity to learn about key […]
On December 16, 2011 the Department of Health and Human Services (HHS) released a bulletin outlining proposed policies on how states will implement aspects of healthcare reform, also known as [...]
As reported by the New York Times on December 10th and by a wide variety of other media outlets, medical researchers in Britain have successfully used gene therapy to treat […]
Nearly 300 members of the local bleeding disorders community came together on December 4th for a day of laughter, learning and lunch at the New York City Hemophilia Chapter 2011 […]
