Meet Dr. Emily Carter, a leading expert in Wilson’s Disease, dedicated to advancing research and providing compassionate care to patients and their families. With over 20 years of experience, Dr. Carter has been instrumental in developing innovative treatment strategies and fostering a supportive community for those affected by this rare genetic disorder.

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WDSG-UK’s Coffee Morning 1st March

WDSG-UK’s Coffee Morning 1st March

Feb 27, 2026 |

WDSG-UK's Coffee Morning 1st MarchWDSG-UK is hosting a Coffee Morning via Zoom on Sunday, 1st March 2026 to mark Rare Disease Day 2026 (Feb 28th). The first Rare Disease Day was introduced by the European Organization for Rare Diseases back in 2008 and was scheduled...

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Dingbat Competition Results 2025

Dingbat Competition Results 2025

Feb 2, 2026 |

Dingbats Results and Answers 2025Results of and Answers to the WDSG-UK 2025 Xmas Dingbats Competition Thank you to everybody who took part in the Xmas-themed Dingbats competition, which has raised an astonishing £675 for the Group and especially to those who bought...

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Rare Disease Day 2026 Zoom Meeting

Rare Disease Day 2026 Zoom Meeting

Jan 24, 2026 |

Rare Disease Day 2026 Zoom MeetingAnnouncing the date and time for our annual Zoom meeting to celebrate Rare Disease Day 2026. The meeting will be held on Sunday, 1st March 2026, from 1100–1200 - by invitation only. Anybody interested in attending who hasn’t received...

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