My Support

To create more awareness about laryngeal cleft we created various platfroms (support groups) for you in case your child has been diagnosed (or with suspicion of) with a laryngeal cleft. This way we hope you can exchange experiences and information about laryngeal cleft.

You can create your own accounts and start getting in contact. We hope you find enough valuable info on our support group and site! We are always open to when you have any just mail us:

Start sharing
In case you have useful laryngeal cleft documentation we'd like to hear it and when possible receive a copy so we can publish the documents on our page.

You may also follow:

Hope to welcome you soon!