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Sites 11-19 of 19
  1. Cleft Lip and Cleft Palate Resource. Includes mailing list, webring, photo gallery and a huge collection of resource articles.
  2. Provides education, inspiration, support and understanding for parents and families. Also offers insurance and advocacy information.
  3. Providing assistance with the management of children's cleft or craniofacial anomaly.
  4. The FCPA is a state-wide association of healthcare specialists and parents who welcome opportunities to help children with a facial difference.
  5. Meet other local families affected by cleft lips/palates for support, info, and general conversation.
  6. This information is by Virginia “Ginny” Dixon-Wood who has worked in the area of oro-facial speech disorders for 25 years. Ms. Dixon-Wood is dedicated to educating parents and
  7. Coming Soon! This site is under construction.
  8. CleftPALS is a national organisation of parents and professionals involved in the treatment of the cleft condition. We all volunteer our time and efforts to provide information and
  9. SC Center for Cleft Palate/Craniofacial Disorders. Member of the Medem Network: Connecting Physicians and Patients Online.

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