In support of #GenomicsConversation week, we are delighted to share this Voices blog by Sally Shillaker, Practice Development Lead – Genomics at iHV, about the launch of our exciting new Genomics Ambassador Programme. buff.ly/4eycolp NWGMSA Genomics Education

We take a look at some contemporary GMSA/GLH projects that have helped the #NHS along in its journey of #genomics. buff.ly/3VwIEN0 #GenomicsConversation

Day 3 of the #GenomicsConversation is all about 'Ticket to ride: The patient journey'. We spoke to Jo Wright to learn about her experiences as a parent carer and why #genomics has played such a vital role in her daughter's healthcare 👇 buff.ly/3VwuqM6

Meet Ian, who has witnessed the development of a gene-directed therapy for his condition, tuberous sclerosis complex, within his lifetime: buff.ly/3ze9AJX #GenomicsConversation

For Debbie and her daughter Emma, genomic testing for #cancer has been a rollercoaster ride affecting the whole family. Hear their story here: buff.ly/4cxiJvx #GenomicsConversation

Menopause isn't a health condition, it’s a stage of life. Improve your knowledge of the menopause and how it may affect you or someone you work with by completing our e-learning module. ➡️ e-lfh.org.uk/programmes/men…

Meet Beskida and discover what having a diagnosis through whole exome sequencing has meant to her and her family: buff.ly/4cjMO1W #GenomicsConversation

Not everyone’s journey to diagnosis is a simple one. For Loretta, a mother of two, being diagnosed with #FabryDisease was the result of a long and challenging #DiagnosticOdyssey. buff.ly/3VYAcHO #GenomicsConversation

‘Ticket to Ride: The Patient Journey’ It’s Day 3 of #GenomicsConversation week, and Lead Midwives Beth Shobbrook of NHS South East Genomic Medicine Service and Tina Prendeville 💙 of the North Thames Genomic Medicine Service explore how midwives help families navigate their #genomic journey. Read more: ney-genomics.org.uk/lets-talk-geno…

Day 4 of #GenomicsConversationWeek, and today is all about unchartered journeys: what lies ahead? To examine this, we spoke to Jennie Bell, Consultant Clinical Scientist and CAS GLH Operational Director, to learn where research could lead us 🔬 buff.ly/3VNADEE

We know #genomics is making a difference today, but how might #RareDisease testing pathways evolve in the future? Hear from consultant clinical geneticist Dr Frances Elmslie in our film: buff.ly/3xpfA25 #GenomicsConversation

Are you interested in diversity within the genomics community? Today at 12:30, West Midlands Genomics Laboratory's D&I lecture series continues, with Waheeda Rahman and Nour Mahfel sharing their stories. Register here 👇 events.teams.microsoft.com/event/0476551c…

Through the Clinical Pathway Initiative, we are helping clinicians to identify the knowledge and skills needed to deliver genomic testing to patients now and in the future. Discover the available and upcoming pathways: buff.ly/45Kq2hg #CPI #GenomicsConversation

Today we're exploring what lies ahead by revisiting January's blog, which covered new research indicating how whole genome sequencing, in combination with clinical data, could help to personalise cancer care. Read here: ow.ly/q9Pu50SgSg1 Genomics Education #GenomicsConversation

‘Uncharted Journeys: What Lies Ahead?’ For Day 4 of #GenomicsConversation week, waheeda abbas of North West GMS and Karen Creed of Central & South GMS think about the future of genomics in maternity care. Read more here: ney-genomics.org.uk/lets-talk-geno…

Today we’re at the Queen Elizabeth Hospital in Birmingham, speaking to HCPs and the patients about #genomics and why it matters #JeansforGenes

What is non-coding DNA and what does it do? 🧬 Read the latest blog to find out, linked below. ow.ly/QMzt50Tq0Vr #Genomics #DNA

Jamie Theakston's bravery in speaking up about cancer may have saved lives - prompting one person every 16 seconds to check symptoms on our website. Today I'm in Birmingham with Wes Streeting seeing one of our cancer buses that go into communities to improve early detection. ⬇️

Are you interested in EDI within genomics & the wider healthcare sector? Join us on 29 October for an exciting webinar, where we will hear from experts on the current state of play, emerging research, and what's happening to improve the healthcare sector for minorities in the UK

We have begun testing newborns for over 200 rare genetic conditions as part of a world-leading study in NHS hospitals. If we can diagnose and treat children for rare genetic conditions years earlier and help stop them in their tracks — it will be transformational for patients.