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.

Order your official walk t-shirt today so you and your team walk can in style!

Apply today for FFC's 2026 Scholarship! All application materials should be submitted to: scholarship@facesofchildren.org in PDF format by midnight on March 1, 2026. See Here for more information on who qualifies for the scholarship and how to apply.

Please join the Mulliken Family for a memorial celebration in honor of John B. Mulliken, M.D.. Patients, family, friends, colleagues, and all others are welcome to join for any or all portions of the day. In-person session information:   Saturday, April 25, 2026 8:30 a.m.—4:00p.m. The Joseph B. Martin Conference Center Harvard Medical School 77 Avenue Louis Pasteur Boston, Massachusetts   8:30 a.m. Reception 9:00 a.m. Tributes 12:00 p.m. Luncheon 1:00 p.m. Remembrances   Virtual joining information: Topic: Memorial Celebration for Dr. John B. Mulliken, April 25th, 2026 Time: Apr 25, 2026 09:00 AM Eastern Time (US and Canada) Join Zoom meeting: https://harvard.zoom.us/j/96739694205?pwd=6s5r3XSCXahdwUZxkETNQU61mqhvcA.1 Password: 046559

We are excited to announce that FFC will be sponsoring four kids to attend Kenzie’s Camp! Kenzie's Camp is an overnight summer camp designed specially for children and teens ages 8 to 16 born with craniofacial differences. It offers a safe, supportive environment where campers can enjoy being kids, build confidence, and connect with peers who share similar life experiences. Led by young adult counselors and mentors who also have craniofacial differences, the camp features a wide array of outdoor adventures, including zip-lining, climbing, boating, archery, and arts and crafts, alongside meaningful team-building activities. When: June 20-23, 2027 Where: Camp Hazen YMCA, Chester, Connecticut 06412 Deadline for FFC Sponsorship Application: January 1, 2027 If chosen for sponsorship, FFC will fully cover the cost of camp registration. How to apply: Please complete and email the 2027 Kenzie's Camp Sponsorship Application and photo release form to communications@facesofchildren.org by January 1, 2027 to be considered for sponsorship by FFC to attend Kenzie's Camp. Please note: Applicants must be a resident of one of the six New England states to be eligible for FFC sponsorship. How sponsorship works: FFC will communicate directly with Kenzie's Camp to get campers registered, and will pay the camp directly for the cost of attendance. For campers who are selected: By accepting FFC sponsorship, you also agree to share pictures with us and write a story about your experience for use in our newsletter, website, and other promotional needs. If you have any questions about the FFC sponsorship application process, please reach out to communications@facesofchildren.org.