David Wilkins
David Wilkins has joined us as an NDF Mentor. David has Norrie Disease and says ‘Even I still can’t quite believe it!’ David is blind with no light perception at
Blog
Teddy’s journey so far… On the 24th March, 2016 at 8:14am we welcomed our beautiful baby boy Teddy into the world. He was amazing and everything that we could have
Family Stories
The Norrie Disease Foundation‘s Medical Advisory Board and Wendy Horrobin
 PreviousNextThe Norrie Disease Foundation‘s Medical Advisory Board and Wendy Horrobin celebrating the start of the NDF’s exciting venture. Ethan Peacock, aged 12 – Formally launching the Norrie Disease Foundation –
News
PreviousNext Christopher was born 13th December 1994. At birth, there were no signs of any disabilities. When Chris was 6 weeks old, he came down with signs of a bad
Family Stories
Carla Danielle Golledge, mum to Cameron, who has Norrie disease shares an incredibly powerful account of her family’s journey. I was asked to write a few words about Cameron and
Blog