Resources- Specific Diagnosis Card Catalog- Cleft Palate / Cleft Lip


  • Who to Contact
  • Where to Go to Chat with Others?
  • Learn More About it
  • Links
  • Who To Contact

    Wide Smiles
    P.O. Box 5153
    Stockton, California, USA, 955205-0153
    209-942-2812
    209-464-1497 (fax)
    E-mail: josmiles@yahoo.com
    Web: www.widesmiles.org

    Wide Smiles provides information, inspiration, and support for persons affected by cleft lip and/or cleft palate. They have pamplets for new parents "How different is Anthony", and "Anthony Visits his Cleft Palate Team", and are planing a parent-to-parent matching program in the near future.

    Where to go to Chat with Others?

    Cleft-Talk
    Cleft-Talk is an online discussion list that will link you to other families around the world who are dealing/have dealt/will deal with the very same challenges that you face today.

    Wide Smiles Conference Room
    Real Time Chats

    Cleft Kids
    This list is for parents of children with cleft lip or palate.

    Cleft Chat
    For parents of children born with cleft lip and/or cleft palate. Our list is open to all to freely express their feelings, get support and to learn in a positive environment.

    Learn More About It

    What Happened? - A Look at the Causes of Clefting

    Cleft-Links : Answers To Questions & More

    MEDLINEplus: Cleft Lip and Palate

    Links

    Wide Smiles Web Site
    Cleft Lip and Palate Resource

    The Cleft Lip and Palate Association - United Kingdom
    This site answers some of the most commonly asked questions about cleft lip and palate and provides information on the services and advice offered by CLAPA - The Cleft Lip and Palate Association.

    Cleft Lip and Palate Association of Ireland
    A voluntary group formed to provide support and information for parents of children affected by cleft lip and palate and those directly affected by the condition.

    Prescription Parents
    Parents helping Parents of children with cleft lip & palate

    Smiles
    "SMILES" is a group of dedicated families who have developed a first-hand understanding of the needs of children with cleft lip, cleft palate and craniofacial deformities.

    Cleft Palate Foundation
    A non-profit organization dedicated to optimizing the quality of life for individuals affected by facial birth defects.

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