The Trisomy 18 Foundation has a network of lay and professional spokespeople ready to address questions from the media and available for interview on a number of issues:

Participants in the Trisomy 18 Foundation's network of support groups across the country who

• are currently or have been pregnant with a Trisomy 18 child
• are raising a surviving Trisomy 18 child at ages from 1 to mid-30s
• are attempting or have succeeded in having another child after having a previous child with Trisomy 18

Our Founder and Executive Director is also available for interview on a variety of topics:

• adverse prenatal diagnoses in pregnancy
• perinatal and neonatal loss
• parental bereavement issues after loss of an infant
• chromosomal disorders
• perinatal hospice practices
• prenatal testing
• online community building
• advocating for rare disease organizations and their affected families

To arrange for an interview, please contact:

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Expert Opinions
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For Parents: Tips for Talking with the Media
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