Events from South East Genomics

Join us for a our final event of Rare Disease Week to hear from Dharmisha, Mum to Sebastian, who was the 6th child in the UK to receive treatment for Spinal Muscular Atrophy (SMA) Type 1 in 2021. 

Join us for a webinar to hear from the amazing Diana, Mum to Sebbie, a 10 year old living with SHINE Syndrome, a rare genetic condition affecting around 250 people worldwide.

Ever wondered what it is like to navigate life with a rare genetic condition? Hear directly from the amazing Charlotte Doody, Mum to Maisie who has Cardiofaciocutaneous Syndrome (CFC).

Discover how genetic testing is helping doctors link genotypes and phenotypes in liver conditions like cholestasis

Are you considering a career in genomics? Learn more about what it’s like to work in our labs and get tips for your application at our virtual open day!

Join us for the latest instalment of our Lunch & Learn series! This month’s topic is on inherited cancer and the important role that nurses play in patient care.

Join us to find out about the new testing pathway for the South East. If you order ctDNA testing, or plan to in the future, this is an essential education session.

Join us to find out about the new testing pathway for the South East. If you order ctDNA testing, or plan to in the future, this is an essential education session.

Join us for the latest instalment of our Lunch & Learn series! This month’s topic is on Huntington’s Disease, with a focus on care coordination and treatment advancements!

We are pleased to invite you to our free education session and the latest in our Rare Disease Series,  Thalassaemia: Clinical Manifestations & Genomics.