More Online Resources
A list of other useful websites with information about Cleft Lip & Palate and related conditions.
- Changing Faces
- UK organisation offering information and support to children and adults who have facial disfigurements.
- Face Forward
- Home to message boards for people affected by cleft lip and palate and an online chat room.
- Cleft Lip and Palate Association of Ireland
- Irish organisation offering information and support to individuals and families affected by cleft lip/palate.
- Eurocran International Support
- European collaboration on craniofacial anomalies. Links to support groups in European countries.
- Cleft Palate Foundation
- US organisation offering information to parents of babies born with clefts and other craniofacial anomalies and to health care professionals who are involved in the care of affected infants.
- CleftPALS QLD Inc
- Cleft Palate and Lip Society, Queensland Division, Australia.
- LKG-foreningen in Stockholm
- Swedish organisation for people born with cleft lip/palate, parents of young children and health professionals.
- Wide Smiles
- US organisation offering information and support to individuals and families affect by cleft lip/palate.
- Wolfgang Rosenthal Gesellschaft
- German self-help group for families affected by cleft lip and/or palate.
- I CAN
- A childrens communication charity who work to develop speech, language and communication skills for all children.
- Talking Point
- Talking Point is a website all about speech, language and communication difficulties in children. It has a range of information and resources for parents and carers of children and also for professionals.
- The Cleft Club
- This is an interactive US club for people affected by cleft lip/palate. There are different forums where messages can be read and posted.
- Cleft-Support
- US interactive site for teens.
- American Cleft Palate-Craniofacial Association (AC
- US based international association of health care professionals involved in the treatment of and research into cleft lip, cleft palate and other craniofacial anomalies.
- Max Appeal
- UK support group for families affected by DiGeorge Syndrome.
- 22q11 Group
- Group formed by parents of children with Velo Cardio Facial Syndrome/Sprintzen Syndrome/Di George Syndrome
- Stickler Support Group
- UK organisation offering information and support to individuals and families affected by Stickler Syndrome
- UK Self Help Groups
- Index of self help groups in the UK
- Active Birth Centre
- Information on many aspects of pregnancy and birth, breastfeeding and babycare.
