We are glad you found this site and
hope that it will provide you with the necessary
resources and support you need to assist you in your
journey with your special Cranio Kid.
In March
2008 my son Cameron was born and diagnosed with
Craniosynostosis. After spending many hours researching
information on craniosynostosis in South Africa, the
results were fruitless. In addition we were trying to
deal with the trauma of the diagnosis and desperately
wanted a better understanding of Cranio. Cameron had his
first procedure on the 25th July 2008, after a great
deal of support and encouragement from family, friends
and complete strangers, a decision was taken to form a
South African website that can provide others parents
with information on Craniosynostosis and hopefully this
will assist them in their Cranio Journey.
For more information or support, please contact Robyn
Rondi on -
robyn.rondi@hotmail.com or 082
601 8585
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