At the age of 12, Abby Gardner was diagnosed with a rare disease called Wolfram syndrome. At the time, there was very little information available about the condition. Since her diagnosis, Abby has been supported by and worked alongside some incredible individuals. She has gone on to become a trustee of WSUK and has taken part in multiple clinical trials.
Today, a better understanding of Wolfram syndrome — and other rare diseases — is beginning to emerge. This progress would not be possible without listening to those affected, whether patients themselves or their loved ones. It is also thanks to the vital work of clinicians and researchers. By working together, patients, families, clinical staff, doctors, and researchers are developing clinical trials that place patients at the heart of their work, with the hope of one day developing effective treatments for conditions like Wolfram syndrome.
