A woman who found a lump could wait up to twelve weeks to learn whether she had breast cancer. We redesigned the diagnostic pathway with the clinicians who run it. It is now the national standard in Norway.
Short read

For a woman, she becomes a patient the moment she finds a lump. For the hospital, she only became a patient once cancer was confirmed. Everything followed from that gap. Appointments and tests were scheduled department by department, each one sensible on its own, and the weeks disappeared in between because the time before diagnosis belonged to nobody.
She was already a patient. The system just had not noticed yet.
Interviews and observation with patients, clinicians and the staff who book the appointments. Not what the pathway says on paper, but what actually happens to a person moving through it.
Journey maps and service blueprints that put the patient experience and the hospital process on the same page, so decision makers could see exactly where the time and the information were lost.
In co-design workshops, clinicians and leaders rethought routines they had followed for decades. We did not arrive with answers. We built the evidence and the confidence for them to change the system themselves, which is the only version that survives contact with a real hospital.
Supporting the new process until it worked in daily practice rather than only on the blueprint.


Time to diagnosis fell from up to twelve weeks to six days, and the process became the national standard for breast cancer in Norway. It won the Norwegian Award for Design Excellence and IxDA recognition, was cited by the OECD and published as a case study in This Is Service Design Doing.
This project is the reason I believe the biggest improvements come from redesigning the system around the person, not from better screens. It is still how I work.