OATSA South Africa Support Group for Children Born unable to Swallow

Being told that your child will be or are born with a congenital abnormality is hard. If the diagnosis is oesophageal atresia the fear becomes greater especially if the condition is unknown to you.

We are a group that aims to help all patients and families. We try to connect with each other, share stories, ask questions and above all make sure that everyone knows…

OATSA South Africa Support Group for Children Born unable to Swallow

OATSA is a non-profit organization.

This group is for all the children and families of patients born with an oesophageal atresia and/or a TOF in South Africa. All adult OA and TOFS also welcome.

We have no need to feel alone. Support makes it so much easier.

We have a large support system in South Africa and this group is to try and get everyone together to understand the disease and join the journey together. Any questions or comments can be posted here. We are one big family.

“…because being born unable to swallow is hard enough.”

Kids born with Tracheoesophageal Fistula (TEF) & Esophageal Atresia (EA)

Because being born unable to swallow is hard enough, no one should ever feel alone

FACEBOOK GROUP

Private

Only members can see who’s in the group and what they post.