Our son has a Laryngeal cleft type I. He is now 5 years old. At the age of 14 months his cleft has been repaired.
Laryngeal cleft is a very rare congenital anomaly of the larynx and little is know about it.
Good information on future developments about the laryngeal cleft is hard to come by. And doctors can not tell us what to expect!.
That is whay we launched a website for our son and his laryngeal cleft. http://www.diegojulian.nl or http://www.laryngeal-cleft.com.
The objective of this site is to inform parents by parents. Exchanging information and eachothers experiences regarding the laryngeal cleft and related issues of their children.
So if you have children who have a laryngeal cleft and or a related anomaly we invite you to visit our website http://www.diegojulian.nl
Would you like to create your own account and get in touch with other parents as well please let us know via our contact form on our site.
or mail firstname.lastname@example.org
Hope to see you at our site!
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