September 16, 2026
12pm
Finding your way: A Parent’s Guide to Rare Disease
Join us on September 16th 12-1pm to launch a new guide for parents on navigating a diagnosis of a rare genetic condition
September 16, 2026
12pm
Finding your way: A Parent’s Guide to Rare Disease
Join us on September 16th 12-1pm to launch a new guide for parents on navigating a diagnosis of a rare genetic condition
October 9, 2026
12pm
What would you do if your patient got a genetic result you weren’t expecting?
Join us on October 9th 12-1pm for a session on how to prepare for genetic result that reveals incidental findings
May 15, 2026
9am
Cardiology and Genomics Study Day
Join us on Friday 15th May for a free, educational study day in London to learn more about how genomics is shaping the future of cardiology practice with the opportunity to hear patient perspectives.
March 5, 2026
12PM
Cardiomyopathy & Genomics : changes to the genomic testing pathway
Join us on 5 March at 12:00pm and register for the session to ensure you’re ready for the changes to the genomic testing pathway for cardiomyopathy.
Join us on Monday 2 March at 12pm to explore the genomics of familial pneumothorax, including insights for clinical practice.
March 26, 2026
12PM
Beyond Mendel : join the discussion at our Genomics Festival
Join the debate at our Genomics Festival on March 26th at midday.
Leading the debate will be renowned genomic experts including Professor Richard Thompson, Dr Adam Jackson and Professor Caroline Wright and chaired by Dr Frances Elmslie, Clinical Director of the South East Genomic Medicine Service.
February 27, 2026
12pm
Rare Disease Week: In conversation with… Dharmisha, Mum to Sebastian
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.
February 25, 2026
12pm
Rare Disease Week: In conversation with… Diana, GP and Mum to Sebbie
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.
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