Sue with a bouquet of flowers.

Sue Ricketts


Sue has served in various volunteer roles with the Nystagmus Network including Parent Adviser and Trustee since 1991, when her baby daughter was diagnosed with congenital nystagmus. She joined the charity’s staff team in 2015. She is passionate about lifelong learning, equal opportunities and improving life for people living with nystagmus.

Read more about Sue here

Willow.

Willow Horner


 
Willow has been involved with the Nystagmus Network since she was a child; her lived experience as a partially sighted person has provided a rich understanding of the importance of advocacy and support for those living with nystagmus. Alongside her master’s degree studies, Willow undertook various roles in disability advocacy, developing a keen interest in matters of equality, diversity and inclusion in academia and beyond.
Â