Emma shares her Lynch story
I’m grateful that I’ve been diagnosed with a genetic condition.
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Tracy’s talks to us about Lynch Syndrome
“That decision to get tested opened a giant can of worms, but it saved my family from any further loss.”
Kirsty’s experience of being diagnosed with a rare disease
When Kirsty was diagnosed there were only 60 other people in the world with the same condition as her.
Mel Dixon : one parents story
Discovering our children have a rare genetic mutation has opened new doors for the future
Alan’s Lynch Syndrome story
Genomics has helped me to understand why my family keep getting cancer
Sheila & Mark’s VHL journey
I’ve had 27 surgeries in 27 years……and counting
Andrea is determined to raise awareness of Lynch Syndrome
I’m thankful that I don’t have to go through what Mum had to.
Adam’s one man mission to get a diagnosis for his children
Read Adam's story about seeking a diagnosis for his children who were the first in the UK to be diagnosed with CRELD1.