Stephen WILSON Obituary

Steve was a passionate advocate for Kiwis living with Lynch Syndrome, particularly in the area of medicines access. A humble family man, public speaking did not sit comfortably with Steve, yet he spoke publicly on numerous occasions about the lack of funded medicines for Lynch syndrome patients. In 2019 he presented his petition on the steps of Parliament calling for Keytruda to be funded for Lynch syndrome patients. Although Keytruda saved his life, Steve did not think it fair that it was only available to people who could afford to pay for it, so rather than sit back on his laurels he decided to do something about it. With his wife and best friend Karen always by his side, Steve remained a staunch advocate for New Zealand Lynch syndrome patients and his legacy will remain with our group for many years to come. Our thoughts are with Karen and the whole Wilson whanau at this difficult time. From the Lynch Syndrome community in New Zealand.

Sad to hear about Steve. Such a good bloke who fought a good fight. Condolences to Karen and family. Mark Harvey.