24 episodes

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.

The ME Show Gary Burgess

    • Health & Fitness
    • 5.0, 35 Ratings

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

    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.

    • 46 min
    Special Edition - The Real ME

    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.

    • 29 min
    Episode Ten - Dr Mark Guthridge

    Episode Ten - Dr Mark Guthridge

    Gary Burgess speaks to Australian medical researcher Dr Mark Guthridge, who himself has lived with ME since 2015.

    • 28 min
    Episode Nine - Carol Monaghan MP

    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.

    • 17 min
    Episode Eight - Dr Nina Muirhead

    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.

    • 22 min
    Episode Seven - The Countess of Mar

    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.

    • 19 min

Customer Reviews

5.0 out of 5
35 Ratings

35 Ratings

Lefty Burns ,

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!

RyMcD3 ,

Wonderfully done

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

SusanFromTheStates ,

scientist

Gary, this is really powerful, thank-you. A clear biomarker is near, and your podcast will be part of the media that was involved before this disease has an appropriate household name.

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