Our Team

Our Team

Meet the NDF Team

The NDF was created in 2017 by 3 families who connected because they each had a son with Norrie Disease.  Since then they have directly raised over £190,000 which has been spent on research and family support.

Wendy Horrobin
Wendy is Chair, Coordinator and Co-founder of the Norrie Disease Foundation. Her role includes ensuring the board fulfils its legal requirements. She is also a spokesperson for the charity; driving the Norrie Disease Foundation forwards.
Meet Wendy HorrobinChair »

Medical Advisory Board

The Norrie Disease Foundation is guided by the Scientific Medical Advisory Board in scientific matters including research efforts and direction. Our board consists of renowned experts in the field and we are very grateful to them for giving their time and expertise to the Norrie community.


Our Ambassadors

The NDF is lucky to have 4 fantastic ambassadors to support our cause.

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