Here is a link to this article; it may be of interest to you.
http://www.nih.gov/news/health/may2010/nidcr-03.htm
Sunday, June 6, 2010
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A place to learn and share for parents and families of children with clefts
NOTE
The information and opinions on this blog come from parents, and the blog is not associated with Primary Children´s Medical Center or any other institution.
Welcome!
This site is specifically for parents of kids with clefts being treated at Primary Children's Medical Center in Salt Lake City, Utah, but I hope that there will be information that is helpful to all parents of kids with clefts. If you are just starting to learn about clefts, I would suggest starting with the "General Information" topic and going from there. To find information on a specific doctor or topic, click on one of the links on the right. You can also search the blog using the box below the topic list. If you have information or experiences to share, please leave comments or contact me to do a guest post at kidswithcleftsblog@gmail.com. Thanks for visiting!
Spanish Version
Topics
- Adoption (2)
- Arm Restraints (7)
- Before and After (10)
- Doctors at PCMC (9)
- Dr. Kjar (1)
- Dr. Morales (8)
- Dr. Motoki (1)
- Dr. Muntz (1)
- Dr. Schmelzer (1)
- Dr. Siddiqi (4)
- Dr. Warnock (2)
- Feeding (8)
- General Information (4)
- Helpful Products (3)
- Helping Out (1)
- Humor (3)
- In the News (1)
- New Studies and Research (3)
- Pacifiers (2)
- Parent Experiences (11)
- Pierre Robin Sequence (3)
- Pumping (5)
- Sleep Apnea (2)
- Surgery FAQ's (13)
- Velo-Cardio-Facial Syndrome (Deletion 22) (1)
Search The Blog
Related blogs, groups, and sites
- AmeriFace
- Baby Center Cleft Group
- Children's Craniofacial Association
- Cleft Advocate
- Cleft Line
- Cleft Notes
- Cleft Palate Foundation
- Cleft Palate-Craniofacial Journal
- Kids With Clefts Utah on Facebook
- Pierre Robin Network
- Pierre Robin Support Group
- Teeter's Page on Apert Syndrome
- The Brady Report
- The Face of Change