‘We believe this is the miracle cure and we cannot wait years until it is sanctioned’ It bears all the hallmarks of a horror movie – being told that a loved one will die in a few months unless you can come up with a large sum of money: $78,000 to be precise. But for Canterbury mum-of-four Sally-Anne Davis and her family, this is the stark reality.
There is, however, no masked phantom – just a little-known hereditary cancer gene called Lynch syndrome, which is attacking the immune system of her husband Jack, the father of their four children, Thomas,
(21), Aimee-Anne (20), Poppy, nine, and Hunter, six.
The family has been told that Jack’s only chance of survival is a drug called Immunotherapy pembrolizumab, which has not yet been…
