More Than You Can Imagine: Genomics and Rare Disease

Join Central and South Genomics for an insightful webinar in recognition of Rare Disease Day, where we bring together patients, healthcare professionals, and researchers to explore the latest in patient advocacy, genomics and rare disease. This event is for everyone, whether you're from a healthcare background, have been affected by a rare disease, or are just keen to learn more.

This session will cover key topics, including:

• Understanding rare diseases and genomics – How advances in genetics are shaping diagnosis and treatment.

• Equity & diversity in research – Addressing challenges in representation and access to care.

• Patient experiences – Real-life stories that highlight the journey from diagnosis to treatment.

• Newborn research & pharmacogenomics – The future of personalised medicine.

• Support networks & advocacy – Connecting patients with resources for ongoing care.

We'll hear from a range of experts, from clinicians to charity representatives and patient advocates. To view the full agenda, please click here. 

If you have any queries, please don't hesitate to get in touch. We look forward to seeing you on 28 February.