Twenty year-old Sarah Laing has Cystinosis. Her story and the research being undertaken at Sunderland University, not far from where Sarah lives, are told on a short ITV television broadcast. To see the full video, please visit ITV.com.
The Cystinosis Foundation UK has helped fund the projects at Sunderland and this story highlights the importance of research and the difference it could make. We thank everyone who helps raise money for the Foundation so we can continue to support such projects!