Here in New Zealand, clinicians and advocates are pushing our country’s government to update its genetic editing and…
Articles by Jaime Christmas
Through my roles as a caregiver for my late husband, Aubrey, and as an amyloidosis patient advocate, I’ve been…
It’s another stunning summer day here in New Zealand’s Waikato region. We’ve been blessed all week with clear skies and a…
December is a month of university graduation here in New Zealand. All the hard work, blood, sweat, and tears conclude…
According to the Murdoch Children’s Research Institute, there are more than 7,000 rare genetic diseases in the world, mostly affecting…
As a columnist for Amyloidosis News Today since October 2020, I’ve written about various topics, all related to my…
My late husband, Aubrey, was diagnosed with hereditary ATTR amyloidosis in 2013 and passed away on May 22, 2022.
Over a year ago, I met someone. Darren James came into my life at a point when I was questioning…
Oct. 26 isn’t just another day; it’s World Amyloidosis Day. As a leader of the New Zealand Amyloidosis Patients Association,…
Since January, the amyloidosis association I lead here in New Zealand has seen our patient numbers grow like never…