Gary Burgess, supported by the ME Association, presents The ME Show for people living with Myalgic Encephalomyelitis or Chronic Fatigue Syndrome, as well as those with an interest in learning more about it.
Special Edition - Severe ME Week
Gary Burgess speaks to Jo Moss who has severe and ME, and benefits advisor Ann Innes, for this special edition of The ME Show to mark Severe ME Week.
Special Edition - The Real ME
To mark ME Awareness Week, Gary Burgess shares the real stories of real people with ME. Hear them describe their own experiences in their own words.
Episode Ten - Dr Mark Guthridge
Gary Burgess speaks to Australian medical researcher Dr Mark Guthridge, who himself has lived with ME since 2015.
Episode Nine - Carol Monaghan MP
Gary Burgess speaks to Carol Monaghan MP, a staunch supporter of people with ME who's arranged a number of Westminster debates - most recently in January this year.
Episode Eight - Dr Nina Muirhead
Gary Burgess speaks to Dr Nina Muirhead who, herself, has ME and now campaigns to raise awareness of it among her medical peers.
Episode Seven - The Countess of Mar
Gary Burgess speaks to the Countess of Mar, who sits in the House of Lords, and chairs the Forward ME coalition of ME charities.
Great resource for M.E.
Great information with professionals that have helped/improved the lives of patients and fighting for us to get us more help
Healthy husband, sick wife, terrific podcast!
I’m a healthy spouse, watching on the sidelines as my wife battles ME. It’s a terrible, horrible, no good, baffling disease. But you probably already knew that. I found this podcast over the weekend, dived in with gusto, and have been filled with sadness hearing the struggles of others (at times to the point of tears), but also feel hope rising as Gary introduces us to so many experts working in diverse fields to move us towards a cure. Pod on, Gary—we’re listening!
Terrific content covering all things at ME/CFS. Gary, the host of the show, does a remarkable job and the guests bring a lot of good information. I just listened to the chat with Dr. Sarah Myhill and she’s just amazing. I’m so thankful for people like her who are doing their best to shine light on, and discover more about, this debilitating illness.
Ryan from California