Hypochondroplasia Foundation
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    • Home
    • About Us
      • About Us
      • Mission
      • Medical Advisory Board
      • Advisory Council
      • Board of Directors
      • Events & Webinars
      • Partners
      • Get Involved
    • For Families
      • Practical Guides
      • Facebook Group
      • Latest News
      • Possible Diagnosis
      • New Diagnosis
      • Understanding HCH
      • Neurological Symptoms
      • Childhood
      • Teenage Years
      • Adulthood
      • Ear, Nose and Throat
      • Treatment Options
      • Family Support
      • HCH FAQ
    • Research
      • Research Overview
      • Clinical Trials
      • Patient Registry
      • Publications
      • Research Participation
      • For Medical Professionals
      • Research Partners
      • Genetic Testing
      • FGFR3 and the Brain
      • Ear, Nose and Throat
      • Library
    • Contact Us
Hypochondroplasia Foundation
  • Home
  • About Us
    • About Us
    • Mission
    • Medical Advisory Board
    • Advisory Council
    • Board of Directors
    • Events & Webinars
    • Partners
    • Get Involved
  • For Families
    • Practical Guides
    • Facebook Group
    • Latest News
    • Possible Diagnosis
    • New Diagnosis
    • Understanding HCH
    • Neurological Symptoms
    • Childhood
    • Teenage Years
    • Adulthood
    • Ear, Nose and Throat
    • Treatment Options
    • Family Support
    • HCH FAQ
  • Research
    • Research Overview
    • Clinical Trials
    • Patient Registry
    • Publications
    • Research Participation
    • For Medical Professionals
    • Research Partners
    • Genetic Testing
    • FGFR3 and the Brain
    • Ear, Nose and Throat
    • Library
  • Contact Us

Advisory Board

Woman smiling at a restaurant.

Carrie Blivice

Carrie Blivice is an American artist, photographer and healing arts practitioner with hypochondroplasia. She is the mother of two teenage daughters and has a deep love of nature. Carrie brings her lived experience, creativity and perspective as a parent in addition to having children with Hypochondroplasia.  








Annie Horner

Annie Horner lives in Atlanta, Georgia, where she works as a Family Specialist at Children’s Healthcare of Atlanta. She has hypochondroplasia and brings valuable lived and professional insights into how healthcare, research and society can better listen to and include people with rare conditions. A childhood cancer survivor and experienced patient advocate, Annie has also served as a consumer reviewer for the US Department of Defense Peer Reviewed Cancer Research Program, helping ensure that research reflects the priorities and experiences of the people it is intended to serve.  









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