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Craniofacial Resources

For families of children in the Craniofacial Center

  • Русский PDF
  • Español PDF

Resources that may be helpful for finding support and information.

The following are support and informational resources for families who have a child with a craniofacial condition. For help with these resources please contact one of the social workers in the Craniofacial Center 206-987-2528.

Seattle Children’s Craniofacial Center website

seattlechildrens.org/clinics/craniofacial/services/surgery/ (English)

A great place to start learning. Includes links to information and support, answers to commonly asked questions, research and advances, recommended reading, glossary of terms, contact information and more.

Craniofacial information stand

Located outside of the Craniofacial Clinic, this stand is kept stocked with information on making the most of your visit, events at Camp Korey, the Social Security application process, general resources and more.

Parent Support Program

This program gives families of children with special health needs a way to connect with an experienced volunteer parent who has been through a similar situation with their own child. Parent matches are made with the intention of providing emotional, practical and informational support. Conversations between parents typically take place over the phone. For more information, see ‘Parent Support Program’ seattlechildrens.org/pdf/pe2674.pdf or contact the Parent Support Program coordinator at 206-987-1119 or email [email protected].

Summer Picnics

Summer picnics are yearly events held at a park or zoo near the hospital. They are a wonderful opportunity to meet other families in a casual, relaxed environment. Kids and families dealing with similar challenges meet each other and find understanding and support. Call the Craniofacial Center for more information about the picnics.

Seattle Children’s Craniofacial Center private Facebook group

facebook.com/groups/craniofacialfamilies/ (English)

This supportive and welcoming community encourages the sharing of triumphs, tributes, issues and concerns. Open only to patients and families of the Seattle Children’s Craniofacial Center, it is moderated by the Craniofacial Center Family Liaison.

  1. If you don’t have a Facebook account, go to facebook.com and follow the directions to create an account.
  2. Log into your Facebook account.
  3. Search “Seattle Children’s Craniofacial Family Chat.”
  4. Click the “Join Group” button.
  5. Receive confirmation message that says, “Request Sent.”
  6. This request goes to the group manager for approval.
  7. Within a week, you will receive a message (via Facebook Inbox) confirming your addition to the group.
  8. Participate by adding something new or helping the group out with what you know!

myFace Organization

myface.org (English)

myFace is an organization committed to transforming the lives of children and adults with facial differences. It provides access to holistic comprehensive care, education, resources and support.

To Learn More

  • Craniofacial Social Work
    206-987-2528
  • Ask your child’s healthcare provider
  • seattlechildrens.org/patient-education

Free Interpreter Services

  • In the hospital, ask your nurse.
  • From outside the hospital, call the toll-free Family Interpreting Line, 1-866-583-1527. Tell the interpreter the name or extension you need.
Seattle Children's Hospital

Seattle Children’s offers free interpreter services for patients, family members and legal representatives who are deaf or hard of hearing or speak a language other than English. Seattle Children’s will make this information available in alternate formats upon request. Call the Family Resource Center at 206-987-2201. This handout has been reviewed by clinical staff at Seattle Children’s. However, your needs are unique. Before you act or rely upon this information, please talk with your healthcare provider.

© 2026 Seattle Children’s, Seattle, Washington. All rights reserved.

01/01/2022
PE1873
Patient and Family Education | Craniofacial

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