This event was originally scheduled for Saturday, March 28, but is being moved to a virtual event.    This event helps consumers understand what current and potential medical advancements (including gene therapy) may mean for you and your family. Information will be presented about hemophilia A, hemophilia B, vWD, and other rare bleeding disorders. Information will also be shared about current insurance barriers and trends, as well as a forum about the psychosocial and emotional implications of change. Agenda Overview…

This is the fourth event during our Virtual Consumer Medical Symposium. To learn more about this virtual series of events, please click here.   About This Session This live session will be held on Saturday, July 25 from 9 AM to 11:30 AM and will include breakout sessions to help you understand more about health insurance, and the psychosocial impact of processing changes. Following these sessions, participants will be able to attend two industry breakout sessions where they can enjoy…

Each year, NEHA is proud to offer programming specific to our Hispanic community. Join us on Saturday, September 19 at the Four Points by Sheraton in Norwood, MA for this event. The conference is filled with educational opportunities for our Latino community members to learn and connect with others. All educational sessions are presented in Spanish only. More information will be released soon.   Registration Will Open in the Summer

This is our largest event of the year, and we invite the entire bleeding disorders community of New England to attend this weekend event. This year, we will be meeting from Saturday, October 24 to Sunday, October 25 at Jay Peak Resort in Jay, VT. Each Fall, the New England Hemophilia Association (NEHA) hosts our annual meeting, called FallFest. This is a two-day event that provides educational programming for adults, teenagers (13-18 years old), youth (6–12 years old), and children…

This event was originally scheduled for Saturday, July 18, but is being moved to a virtual event due to COVID-19. More information will be provided soon. This retreat was developed with community feedback, and is led by professional facilitators and Hemophilia Treatment Center (HTC) partners. The retreat is intended to provide community members living with vWD a chance to learn, network, and ask questions in a more focused setting. Siblings are welcome to attend. More information will be released soon.