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Where can I find other parents whose children have Goldenhar syndrome?

Dr. Jeanne Morrison, PhD
Family Practitioner

There are several support networks for parents whose children have Goldenhar syndrome. Organizations such as the National Craniofacial Association (FACES) and the Goldenhar Syndrome Support Network can help put in touch with other families and local support groups. Talk to your doctor about local resources that can help both you and your child understand and adjust to their symptoms.

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Important: This content reflects information from various individuals and organizations and may offer alternative or opposing points of view. It should not be used for medical advice, diagnosis or treatment. As always, you should consult with your healthcare provider about your specific health needs.