Smile foundation is a non-profit foundation that was initiated in 2002 when a group of friends came together with the intention of giving back to the society. We believe that making a real difference is about bringing the right people together at the right time. our non-profit organization is able to facilitate expert surgical intervention, pre and post-operative care for children living with facial paralysis, cleft lip and cleft palate, craniofacial abnormalities, as well as ear, nose, hand conditions, and burn wounds.
VISSION
We help children live a life inspired by confidence and possibility no matter the circumstances.
MISSION
We transform the lives of children affected by facial abnormalities and severe burns through the best possible surgical and psychological care.
CONTACT US
TELEPHONE
+27 10 753 3034
WEBSITE
EMAIL
ADDRESS
Ground floor
Westwood block 57
6th Road
Hyde park
JOIN US ON OUR SOCIAL MEDIA PAGES
FACEBOOK
TWITTER
INSTAGRAM
YOUTUBE
OUR SUCCESSFUL STORIES
LOGAN PETZER
Logan was born on the 11 January 2018 with a cleft lip & palate. This little hero has undergone 2 surgeries, one to correct his cleft lip and the second to repair his cleft palate. He has just undergone his 18 month check-up & look at the transformation.
PRINCESS
Since 2013, we have been supporting a young girl by the name of Princess. She was born with a bilateral cleft lip and palate. When Princess was just 4 months old, she received her first surgery at Chris Hani Baragwanath Academic Hospital. Up until now Princess has undergone three operations
one cleft lip repair and two cleft palate repairs.
She was due for her fourth surgery last year, which has been postponed because of Lockdown, as all elective surgeries were put on hold.
Princess is now 7 years of age, she is thriving, she exceptionally confident, she loves talking and interacting with other people and gives the biggest hugs.
BABY ALEX
Baby Alex, a bright and cheerful baby boy was born with a cleft lip. He received surgery at R.M.S.A.H (Kimberley Hospital). It is an absolute privilege to see baby Alex after his surgery. Such a special boy who gets to fit in like every other child.
LUNA
Luna, a 14-month old baby who was born with Pfeiffer Syndrome – a complex genetic disorder in which certain bones in the skull join together in early development. This prevents the skull from growing normally, affecting the shape of the head and face sometimes causing increased pressure around the brain. If left untreated, Pfeiffer Syndrome can cause developmental complications such as raised intra-cranial pressure causing recurrent headaches and problems with vision.
Through cranial remodeling, Luna’s skull was re-shaped to allow more room for her brain to grow. Surgery was also crucial under the age of two as Luna’s bones are still soft and pliable, which will make them easier to move to create a normal head shape. This specialized surgery has given Luna a far better start in life.
SMILE FOUNDATION SCHEDULE FOR ANNUAL EVENTS
Smile Movie Night
Join us as we host Smile Movie Night Under the Stars at Walter Sisulu National Botanical Gardens on 25th February 2023.
Bring your family and friends and enjoy the most talked about animation Encanto.
Book now to avoid disappointment
Milky Lane Smile Foundation SPINATHON
Milky Lane Smile Foundation SPINATHON, in association with The Herald Cycle Tour 2023
Get in on the action and spin for an hour to create smiles that will last a lifetime.
- R160 secures your seat, book online
- Great Goody bags for all participants
- Prizes galore
- Limited availability of 50 bikes per hour.
- Online Entries close on Thursday 16 February.
Click Here to Register
PRESS REALESE
DATE : 04 FEBRUARY 2023
TO : ALL MEDIA
FOR IMMEDIATE RELEASE
The Smile Foundation is celebrating turning 22 by bringing more than just smiles to children as they venture into burn reconstructive surgeries.
toni@smilefoundationsa.org
END

