Share
Political powerhouses Beth Rigby, Ruth Davidson and Harriet Harman unite to unravel the spin and explain what’s really going on in Westminster and beyond. Every episode, they will examine politicians, what they stand for and how they sell polices as UK politics enters a new era. They will work out which politicians are coming out on top and who is having an Electoral Dysfunction – and what it all actually means for you. WhatsApp - 07934 200444
…
continue reading
Manage episode 492293563 series 2807868
Content provided by Jack the Insider and Joel Hill, Jack the Insider, and Joel Hill. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Jack the Insider and Joel Hill, Jack the Insider, and Joel Hill or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://staging.podcastplayer.com/legal.
Jack interviews Peter McCluskey - a full time carer and volunteer with EMERGE Australia, a support group for sufferers of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), a complex, long-term illness characterised by severe fatigue that is not relieved by rest, joint pain, multiple food allergies, dizziness, sensitivity to light, touch and sound.
Peter’s wife, Jen, was first diagnosed with ME/CFS in 1993.
Peter outlines the struggles his wife has had to manage over the last three decades. The condition is exacerbated by medical health professionals who often believe ME/CFS is a psychosomatic syndrome. Poor and out-dated advice from the Royal Australian College of General Practitioners continues to worsen the symptoms for sufferers of this debilitating illness.
The advice remains in place in Australia despite changes to treatment in the UK and the US. Sufferers are often bed bound for much of their lives. They find it extremely difficult to access government support, including disability pensions and the NDIS.
405 episodes
))
