Genetic testing gave me the answers that I had been looking for
Getting a diagnosis not only helped Sebastian, it changed the way I listen and care for my own patients.
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People in my community often don’t talk about cancer. If we don’t talk, people die.
“I felt the weight of the taboo when I was diagnosed. I didn’t tell anyone about the breast cancer.”
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.
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).