Cystinosis

  • To improve the care for all patients with cystinosis in the UK
  • To collaborate with the National Designation Centres for Cystinosis
  • To work together with Cystinosis Foundation UK and other patient groups
  • To register every willing patient with cystinosis onto RaDaR
  • To promote research for the benefit of patients with cystinosis, and their families
  • To promote educational resources for patients with cystinosis, and their families

  • Working with the evolving national designation centres and other specialist units to promote equity of access to high-quality clinical care
  • Working with RaDaR to ensure high-quality data capture to enable quality assurance and future research projects in cystinosis
  • Recruitment of patients to the NIHR National Bioresource for Cystinosis
  • Contributing to research in new preparations to treat cystinosis

We work in collaboration with various cystinosis groups around the world, including:

Cystinosis Network Europe

The Cystinosis Foundation UK supports individuals, families and researchers in the Cystinosis community.

RDG Lead(s)
  • David Game, Adult Nephrologist, Guy’s & St Thomas’ Hospital, London RDG Lead
Patient representative(s)
  • Thomas Kenning, Secretary and Trustee, Cystinosis Foundation UK
  • Will Newman, Chairperson and Trustee, Cystinosis Foundation UK
Other members
  • Sally-Anne Hulton, Paediatric Nephrologist at Great Ormond Street Hospital, London
  • Graham Lipkin, Adult Nephrologist, University Hospital Birmingham
  • Lavanya Kamesh, Adult Nephrologist, University Hospital Birmingham
  • Amrit Kaur, Paediatric Nephrologist, Manchester Children’s Hospital
  • Susmito Biswas, Ophthalmologist, Manchester Royal Eye Hospital
  • Muir Morton, Adult Nephrologist, Manchester Royal Infirmary
  • Kate Hillman, Adult Nephrologist, Manchester Royal Infirmary
  • Nabil Melham, Paediatric Nephrologist, Evelina Children’s Hospital London
  • Caroline Booth, Paediatric Nephrologist, Evelina Children’s Hospital London
  • John Sayer, Adult Nephrologist, Royal Victoria Infirmary Newcastle
  • Vicky Moxham, Adult Nephrologist, Guy’s Hospital London
  • Alex Lalayiannis, Paediatric Nephrologist, Birmingham Children’s Hospital
  • Catriona Ryan, Paediatric Nephrologist, Birmingham Children’s Hospital

Some members of the RDG have received honoraria for speaking and/or research grants from Chiesi and/or Recordati Rare Diseases