The Cleft Palate Foundation (CPF) is a 501(c)(3) nonprofit organization dedicated to optimizing the quality of life for individuals affected by facial birth defects. It was founded by the American Cleft Palate-Craniofacial Association in 1973 to be the public service arm of the professional Association.
The mission of CPF is to enhance the quality of life for individuals affected by cleft lip and palate and other craniofacial birth defects.
Fuling Kids International and CPF recently partnered together to place Mandarin subtitles on their feeding video to hopefully better inform and educate caregivers in Chinese orphanages and medical facilities caring for Chinese orphans.
Fiona is a precious little one who is about to turn 3 years old! She was born with Down’s Syndrome and a heart defect known as a PFO. When she was 1 years old, she would sit up on her own, crawl and babble. At the age of 18 months she could stand up with a little support and was babbling and saying simple words. Fiona has been receiving rehabilitation services and she seems to be doing great! She is walking for longer distances while holding onto some support. Fiona is described as being compliant, cute and affectionate. Although her speech is slightly delayed, communication does not seem to be an obstacle for her. Contact one of our matching specialists today if you’d like to learn more about Fiona!
You can contact the China Home Finding Team at (512)323-9595 if you would like to learn more about adopting Fiona. We hope we are able to find Fiona her Forever Family soon!