Max Reid
A couple of Saturdays ago I attended a meeting of Kidney Health New Zealand’s Consumer Council. The Council comprises around 18-20 individuals from around the country, each with kidney disease of varying types and progression. We only meet once a year, and only for around five hours – for those attendees on dialysis, the logistics involved in planning their dialysis around such an event preclude meeting more often or for longer.
Each meeting begins with a round of introductions. How they do that has always been over to the group – but always the format has been the same: name, where they’re from, and the nature of their condition.
“Hi, I’m Ben from Tauranga – on home haemodialysis.”
“Morena. Haami. Northland. In-centre haemodialysis.”
“Hi. My name’s Bridget. I’m from Christchurch, a transplant recipient, but also the mother of a deceased organ donor.”