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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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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Wilson’s Disease Awareness Day 2025

Wilson’s Disease Awareness Day 2025

Dec 4, 2025 |

Wilson’s Disease Awareness Day 2025Each year on December 6th, the global community marks Wilson’s Disease Awareness Day, commemorating the birthday of Dr. Samuel Kinnier Wilson—the neurologist who first described the rare genetic disorder that now bears his name. This...

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