Trisomy 18 Foundation

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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:

Victoria J. Miller,
Executive Director

Trisomy 18 Foundation
4491 Cheshire Station Plaza
Suite 157
Dale City, VA 22193 


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© 2013 Trisomy 18 Foundation. All Rights Reserved.   Trisomy 18 Foundation
    4491 Cheshire Station Plaza, Suite 157
     Dale City, VA 22193
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