ME/CFS on TVNZ’s The Checkup

The Checkup is an eight episode series airing on TVNZ.  

EPISODE 7 will be on air at 8 PM, TV1 on the 1st March  2021.
This episode includes stories :  Colour Blindness, Activated Charcoal , Chronic Fatigue, Placebo and why do onions make us cry? 
It can also be found on TVNZ ondemand after it has aired.

Dr. Ros Vallings features in this episode, discussing ME/CFS.

https://www.tvnz.co.nz/shows/the-check-up

New research shows ME/CFS is not psychosomatic

News articles regarding Professor Warren Tate’s research that shows physiological and biochemical changes and dysregulation in people with ME/CFS compared to healthy controls. Read more here:

https://www.stuff.co.nz/life-style/well-good/300181308/kiwi-researchers-prove-chronic-fatigue-syndrome-is-not-psychosomatic

https://www.nzdoctor.co.nz/article/undoctored/proof-chronic-fatigue-syndrome-not-psychsomatic

Photo Credit: University of Otago.

Richie Barnett and Prof. Tate on Breakfast

Watch Jenny-May Clarkson interview Richie Barnett and Professor Warren Tate on Breakfast (via Facebook Watch).

New Answers for People Suffering with Chronic Fatigue – A new study on Chronic Fatigue Disorder (ME/CFS) is set to help health services better support those living with the disease. While it’s often labelled as depression or made up symptoms, the research confirmed ME/CFS is not a psychosomatic illness. Former rugby league football captain Richie Barnett shares his story with chronic fatigue this morning, along with Professor Warren Tate who has undertaken extensive research.

https://www.facebook.com/Breakfaston1/videos/1001270763701266

Gavin McGregor’s photography project

ANZMES is supporting Gavin in his project and will be using his work
for awareness raising and to advocate for those with ME/CFS. We thank
Gavin for this opportunity.

I am a photographer working on a portrait series on living with ME/CFS.

For this series, I am looking for people who are willing to sit for a
portrait and talk about how ME/CFS has impacted them.

The purpose of the project is to increase awareness and understanding
of how living with the condition impacts people’s lives in a very real
way.

This series will consist of a portrait series and personal stories of
those living with ME/CFS and will culminate in an online exhibition.
As well as ANZMES having the images and stories for their use as a
resource to further their advocacy work.

My partner lives with ME/CFS so I have an understanding of the
condition and a motivation to increase awareness of it.

If you are interested in being involved and telling your story. Please
don’t hesitate to get in touch

Gavin McGregor
0212774788
gavmc23@mac.com
https://www.gavinmcgregor.com

Malcare WordPress Security