Mr Charles Nduka (Acting CEO of Facial Palsy UK)
Charles is a consultant plastic and reconstructive surgeon based at the Queen Victoria Hospital in East Grinstead. He has a specialist interest in facial palsy, and together with colleagues set up a multidisciplinary facial palsy clinic. On hearing patient feedback, Charles realised there was a huge unmet need for support for people with facial palsy. He is passionate about raising awareness of this often devastating condition.
Vanessa is a principal speech and language therapist specialising in facial rehabilitation. Involved in planning the Facial Palsy UK charity since 2010, Vanessa is dedicated to ensuring that everyone throughout the UK has easy access to good quality information about the management and treatment of facial palsy. She set up a Sussex-based Facial Palsy UK support group, the first of its kind in the UK, and is keen to promote similar groups so more people can access informal support and advice within a friendly and caring environment.
Fiona Hawthorne is a visual artist who lives in London with her husband actor Colin Salmon and their four children. Her line drawings grace the pages of Vogue & Tatler, she was artist in residence to the Royal Philharmonic Orchestra, and her portrait of Barack Obama hangs in the Library of Congress. Fiona developed Bell’s palsy in 2010 following a successful operation to restore her hearing. Unrecognised by the out-of-hours GP who ruled out a stroke, Fiona’s journey to seek information, treatment and support began. She is keen to help the charity raise awareness and funds for research.
Alison Sweeting is a qualified accountant with a background in public sector finance and consultancy. She lives in Surrey with her husband and two children. Alison developed facial palsy in 2011 after surgery to remove cancerous tumours in her salivary gland. She was fortunate enough to be able to attend a facial palsy support group very soon after her surgery and found the group invaluable in helping her deal with the physical and psychological impact of facial palsy. Alison is keen to raise awareness of what facial palsy is, its many effects on those who have it and to grow the charity so that it can help support those who live with it every day.
Before taking early retirement Jan managed a large team of staff in a major central government department. Prior to that she had directed and carried out internal investigations. She developed facial palsy following surgery to remove an acoustic neuroma in 2011 and has benefited greatly from the support group run from East Grinstead. She has been involved with the charity from the outset and has a particular interest in raising awareness of the condition and the help that is available.
Gareth is a management accountant with experience in the forensic science and service sectors. Gareth’s daughter was born with facial palsy and for the first 9 years of her life, Gareth and his wife Emma felt isolated, with little support from the NHS. Finding the charity two years ago has helped Gareth & Emma share experiences with other parents, gain advice from adults that have grown up with facial palsy and help their daughter make lots of new friends. Gareth’s goal is to ensure any children born with facial palsy, and indeed their parents, have access to the support and resources the charity has to offer.
Biography coming soon.
Becky is a PhD researcher at the University of Edinburgh, where she explores children’s and parents’ experiences of childhood epilepsy and children’s involvement in their own health care both formally in a hospital setting and informally in the home. Her research interest in children’s experience of medicine and care came from her own experiences of being born with facial palsy and the two corrective surgeries she had growing up. Becky is also a dedicated volunteer having undertaken a number of roles for a range of charities over the last fourteen years. She is currently a trustee for Volunteer Edinburgh and is a Cumberland Lodge Scholar. Becky is a passionate advocate for her community and children and young people.
Sue has a predominantly Commercial Sales and Marketing background. Having spent over 28 years working within the corporate arena Sue took the decision in 2015 when her daughter was born with facial palsy to take some time out to focus on her family. Sue and her partner Les struggled to get information and support from the NHS so quickly turned to Facial Palsy UK. Subsequently Sue became involved in coordinating fundraising events and she is keen to continue doing this to help the charity grow and develop. Sue is dedicated to raising awareness, providing support and guidance to those affected by facial palsy.
Last reviewed: 12-02-2017 || Next review due: 12-02-2018