Events

Join us for a part one of our two-part webinar series involving the prenatal and newborn care of children born with a cleft. Sessions will be broken into two discussion topics each, with a question and answer portions following. In this section, we will hear from professionals regarding the following topics: Prenatal Diagnosis, Tests, and Follow Ups - presented by Olivia Oppel, RN, BSN, CPN, CLC, Clinical Coordinator Maternal Fetal Care Center, Boston Children's Hospital Newborn Care, Feeding, and Screening - presented by Nicolette T. Bushman, DNP, BSN, CPNP-PC, Pediatric Nurse Practitioner, Department of Plastic and Oral Surgery, Boston Children's Hospital   REGISTER NOW

FFC plans to host virtual parent support groups every month. Parents meet and connect with other parents and have a chance to talk, ask questions, support each other and share experiences in a relaxed virtual environment.

Join us virtually via zoom Monday May 27th at 7pm! FFC Young adults, come meet and chat with your FFC peers! Open to young adults 18 and over with a craniofacial condition. This a relaxed virtual meet up designed to connect our FFC young adult community. Get a chance to meet new people, ask questions or just listen whatever works for you!   This month's topic will be: Summer Plans! Register by Sunday May 26th. Register Now  

Join us virtually via zoom Monday June 24th at 7pm! FFC Young adults, come meet and chat with your FFC peers! Open to young adults 18 and over with a craniofacial condition. This a relaxed virtual meet up designed to connect our FFC young adult community. Get a chance to meet new people, ask questions or just listen whatever works for you!   This month's topic will be: How has growing up with a craniofacial condition changed your life? Register by Sunday June 23rd. Register Now  

FFC plans to host virtual parent support groups every month. Parents meet and connect with other parents and have a chance to talk, ask questions, support each other and share experiences in a relaxed virtual environment.

Join us virtually via zoom Monday July 22nd at 7pm! FFC Young adults, come meet and chat with your FFC peers! Open to young adults 18 and over with a craniofacial condition. This a relaxed virtual meet up designed to connect our FFC young adult community. Get a chance to meet new people, ask questions or just listen whatever works for you!   This month's topic will be: How has growing up with a craniofacial condition changed your life? The discussion will then be followed by updates from members who travelled to Washington DC in support of the ELSA Act! Register by Sunday July 21st. Register Now  

FFC plans to host virtual parent support groups every month. Parents meet and connect with other parents and have a chance to talk, ask questions, support each other and share experiences in a relaxed virtual environment.

FFC plans to host virtual parent support groups every month. Parents meet and connect with other parents and have a chance to talk, ask questions, support each other and share experiences in a relaxed virtual environment.

Join us virtually via zoom Monday, February 24th at 7pm! FFC Young adults, come meet and chat with your FFC peers! Open to young adults 18 and over with a craniofacial condition. This a relaxed virtual meet up designed to connect our FFC young adult community. Get a chance to meet new people, ask questions or just listen whatever works for you!   This month's topic will be: How do we educate the public on craniofacial conditions? Register by Sunday, February 23rd. Register Now  

Apply today for FFC's 2025 Scholarship! All application materials should be submitted to: scholarship@facesofchildren.org in PDF format by midnight on March 1, 2025. See Here for more information on who qualifies for the scholarship and how to apply.