The Rare One in a Hundred: John's Delayed Genetic Testing

John's biopsy wasn't sent for genetic sequencing until 9 months after diagnosis

I'm John, a 61 year old retired head teacher. I enjoy sport, gardening, leading history tours and spending time with family and friends.

When I received my diagnosis in 2021, it was Stage IV EGFR+ lung cancer. I had been experiencing a persistent cough, ongoing pain in my chest, neck, upper back and shoulder, and a very quiet wheeze. Not really a misdiagnosis, but my biopsy was not sent for genetic sequencing until 9 months after diagnosis. This was because there was no routine sequencing for squamous patients at the time, though this has now changed. It is quite unusual for squamous lung cancer to have sensitising EGFR - about 1 in 100.

I believe I eat well, exercise regularly, spend plenty of time outside and continue to enjoy contributing to my community through voluntary work. Staying active and engaged has been important for both my physical and mental wellbeing throughout my treatment journey.

"The Trustees of EGFR+UK all deserve medals!”