Laryngeal cleft, fissure of the larynx or interarytenoid cleft is the name of the congenital anomaly which has been diagnosed for our son. The laryngeal cleft is a rare genetic abnormality. Information about laryngeal cleft is very hard to find and doctors can not tell us much as well about the development of the laryngeal cleft.

We created this webiste to bring parents closer which experience the same problems. It is a website for parents by parents regarding laryngeal cleft and related issues.

We have gathered bits of  informatie on laryngeal cleft. Also we have spoke to different parents who have children who unfortunately have laryngeal cleft and other related anomalies.

On our site we try to offer good information and create the possibility to share experiences with other parents.

We all want our children to grow up as healthy as possible!

You will find documentation, usefiul links and descriptions of laryngeal cleft and related anomalies. For sure we are not complete and appreciate it when you have information which you would like to share. You can do that in several ways.

• Request to offer documentation via our contact form
• Shere and post useful links via our contact from
• Ask us a general question via our contact form.

The website will keep on developping and a next step is to create accounts for parents. This will give you the opportunity to tell your story and post blogs about developments and other info you would like to share.

Furthermore you will be able to contact with deffierent parents worldwide who experience similar problems as you are. If you have interest to create an account as well please tell us via our contact form.

Next to the fact that we are dealing with a  heavy subject we would like to keep it as positive as possible and focus on progress. That is why we are going to create a foto gallery as well.