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Welcome to our cleft lip and palate site
You might be thinking this is just another cleft site, but this is a site with a difference, we dont use technical terms, or try to baffle you with science.
we just tell you straight how it is. We are just an ordinary family our special son was born with a unilateral cleft lip and palate. We decided to create this website in the hopes that many other families, friends carers can come here and find support and knowledge, while finding out more about cleft.
If you have any questions please feel free to view our forum. If your answer isnt there, please either post your question on the forum and we shall endeaver to answer your question, if not ourselves then from another member.
Please remember you are not alone!
Membership is free to join the forum
Disclaimer: Please note the information on this site is for reference only, any advice you need should be sought from your cleft nurse, surgeon and other health professionals associated with your childs care.
