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Cornelia de Lange Syndrome Campaign Logo

Cornelia de Lange Syndrome Campaign

Villiers Nel was born on 9 March 2007 in Stellenbosch South Africa.  He was diagnosed as having a defective gene in April 2008. Receiving a diagnosis of Cornelia de Lange Syndrome can be overwhelming.  His expenses are currently at R10000 per month just to keep him alive after head injuries at a care center left him with epilepsy. We need help as a family to cover this. His medical bills reached up to R300 000 per year. No family can carry this type of care alone. The need is to have permanent friends in deed.

To contribute, please select the project below and then the donate button next to the barometer...

 

 

Donor Messages

Anonymous
Julle is in ons harte en gebede