Hypochondroplasia Foundation
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    • Home
    • About Us
      • About Us
      • Mission
      • Board of Directors
      • Medical Advisory Board
      • Events & Webinars
      • Partners
      • Get Involved
    • For Families
      • Practical Guides
      • Facebook Group
      • 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
    • Contact Us
Hypochondroplasia Foundation
  • Home
  • About Us
    • About Us
    • Mission
    • Board of Directors
    • Medical Advisory Board
    • Events & Webinars
    • Partners
    • Get Involved
  • For Families
    • Practical Guides
    • Facebook Group
    • 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
  • Contact Us

Facebook Group

Close-up of a child's hand wearing a green wristband labeled 'CARFIS'.

Facebook Family Support Group

You are welcome to join our private Facebook group designed as a family support group for patients and families affected by Hypochondroplasia. Launched over 10 years ago, this Hypochondroplasia support group has served as a valuable resource for 1500 families from around the world. 


This group is exclusively for patients and their immediate families directly impacted by this condition, not for extended relatives or friends. It provides an essential space for affected patients and families to connect, communicate, commiserate, and support each other.


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