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
communications@trisomy18.org Related Areas:
Press Releases
Expert Opinions
Media Kit
For Parents: Tips for Talking with the Media
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