Everyone in our family was healthy… genetics was definitely not on our radar!
The day Ralf got his liver transplant, it felt like the stars had finally aligned.
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The many different faces of Spinal Muscular Atrophy
SMA Type 3 has changed how I live my life, but treatment, community, and sharing my story have given me hope.
I was just 23 years old when I had a sudden cardiac arrest
Lisa’s diagnosis of Long QT triggered a series of genetic tests for other members of her family too.
I thought my routine of monthly blood transfusions would continue for the rest of my life
Mustafa's life changed when he received the offer to be a part of a gene therapy clinical trial.
Genetic testing helped explain a lifetime of strange things happening to me
No one in my family has Marfan Syndrome, I’m the first.
My cancer was diagnosed through a simple blood test
Charlie found out that she has stage 4 lung cancer through a new revolutionary test that can diagnose cancer through a simple blood test.
Patient-centred care starts with a conversation
Meet Alison, Chair of our People & Communities Committee
David’s rare diagnosis took time, but we never would have got there without genomics.
My son David has a rare condition called Okur-Chung Neurodevelopmental Syndrome (OCNDS).
Lisa’s life changed when two of her sisters died from a hereditary aortic dissection.
Lisa’s life changed when two of her sisters died from a hereditary aortic dissection.
Taking the fear out of Down Syndrome
Meet Sarah-Jane whose daughter Hannah has Down Syndrome.