Your Ultimate Guide for Healthy Living

"In this RNZ investigation, Ruby's mother tells the heartbreaking story of her daughter's fight to be believed, and why she says too many New Zealanders with complex illnesses are still facing the same battle today." https://www.youtube.com/watch?v=XDwJDQUBWDg

Kia ora koutou, Please join me in congratulating the newly minted Dr Peter Tremain, who successfully defending his PhD early this morning. The examination committee has recommended that his PhD be awarded with no revisions. Peter originally joined us at the ABI in 2020 as a Master’s student, and then continued into a PhD supported by a UoA Doctoral Scholarship. He developed and validated custom devices for endoscopic, high-resolution mapping of the electrical activity o

Another young woman fights for her life in hospital while doctors' debate what they see on her scans. So how is it that different doctors can look at the same image and come to completely different conclusions? https://www.rnz.co.nz/podcast/all-in-her-head/double-vision

Health officials make a shock move that sends a ripple of fear through the EDS community. Anusha meets the family of Ruby Hill, who starved to death after a long battle with EDS. And we hear from the experts who say the evidence doesn’t stack up. https://www.rnz.co.nz/podcast/all-in-her-head/do-no-harm

Anusha meets the doctors facing scrutiny for treating Ehlers-Danlos syndrome. Meanwhile, Rachel takes a leap of faith, heading overseas to meet a surgeon who could save her life. https://www.rnz.co.nz/podcast/all-in-her-head/the-zebra-dilemma

Rachel is starving to death, but doctors can't agree what’s wrong with her. In desperation her family fundraises for life-saving surgery she can only get overseas. Rachel has Ehlers-Danlos, a syndrome dividing the medical community. https://www.rnz.co.nz/podcast/all-in-her-head/the-girl-who-could-not-eat

In August , Dr Tim Angeli-Gordon presented to the Auckland Medical Research Foundation. I was fortunate to be able to be in the audience and again humbled by the passion and committment that is required for these projects. Change doesn’t happen without wonderful people dedicating years to research and development. One of Ruby’s Voice Trust missions is to support Research and Development, as per Ruby’s wishes, and we proudly support the innovative work being done by Tim and ot

Dr Tim Angeli-Gordon speaking 8 years ago on the research and development of the Endoscopic Device he and his team are working on and the...

I would like to share the speech OLIVIA ADIE , as Young Enterprise Ambassador, presented to the audience at the Business Hall of Fame...

Dr Tim Angeli-Gordon has won the Royal Society's 2024 Cooper Award for his innovative work on diagnosing and treating chronic stomach...

Jo Hill set up a foundation after her beloved daughter died from a terrible gastrointestinal disease. Now Ruby's Voice is contributing to...

Peter Tremain is a PhD student at the Auckland Bioengineering Institute where he is doing ground-breaking research into diagnosing gut...

One student's success in the search for a link between unexplained gut misery and the electrical pulses in our stomach. Peter Tremain is...

Dr Tim Angeli-Gordon describes his work and the potential of this scholarship

In acknowledgment and recognition of all the people who have had their lives forever changed by Gastroparesis. It's been three years...

Researchers at the Auckland Bioengineering Institute (ABI) have demonstrated that a technique widely used to correct an abnormally...