The Family Experiences Survey for Florida Families of Children with Orofacial Clefts
The Florida Birth Defects Surveillance Program is pleased to announce that we have developed a survey to help families collectively share their experiences in accessing important resources, services, and supports for children birth to 18-years-old born with cleft lip and/or palate. The results of this survey will be used to develop recommendations for improving systems of care here in Florida. We would be very grateful if you could help us reach as many participants as possible.
Please distribute this survey to any parent with a child under the age of 18 who are born with orofacial clefts in Florida. This anonymous survey should take no longer than 30 minutes to complete, and will be distributed throughout the state. Only one survey per family should be completed.
The survey is available online for Florida residents at https://usfhealth.az1.
A Spanish version of the survey is currently under development.
For further information, please contact:
Jennifer Marshall, PhD, CPH Russell S. Kirby, PhD, MS, FACE
Research Assistant Professor Distinguished Professor and Marrell Endowed Chair