“…because being born unable to swallow is hard enough.”
Oesophageal atresia and Tracheo-oesophageal fistula association of South Africa.
Our mission:
- Support patients born with OA/TOF and their families with their emotional journey.
- Connect OA/TOF families in South Africa.
- International connections with organizations globally.
- Raise awareness about this disease.
OATSA IS TURNING 5 in 2024.
Join us for Fun Events throughout South Africa!
We want to raise awareness about oesophageal atresia while having fun with our members. Please support us.
Come and join us for a musical evening of FUN with friends and family at they Barnyard Theatre, Tyger Valley, Cape Town.
Lets celebrate OATSA’s 5th birthday, raising awareness of OA/TOF while having FUN.
6 September 2024
R190 per person or R1480 per table (8pax)
Contact us today for more info
OUR FIRST OATSA FAMILY DAY WAS IN KIMBERLEY THIS YEAR. THANK YOU TO ALL OUR SPONSORS
WATCH THIS SPACE FOR MORE AWARENESS EVENTS IN 2024.
OATSA is a member of a proud member of EAT.
EAT is a federation of member support groups each associated with the rare congenital condition of Esophageal Atresia (EA). Each of the member organisations of EAT operates on a charitable basis in its own country.
OATSA is represented on the EAT board by one of our founding members.
Click on the EAT icon to learn more about this inspiring organization.
Visit any of these other support groups globally.
Click on their logo’s to learn more.
Thank you to all our amazing OATSA sponsors.
Please click on them image to visit their websites.
24 Park Road, Belgravia, Kimberley, 8301
Tel : 053-8325630; Fax : 0865465640 Cell : 0735887600
E-mail: reception@jungnickel.co.za