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.
Just what i needed
As a sufferer it was great to hear the voics of others like me
Please continue to make more!
Amazing podcast with helpful insights on latest progress and also importantly giving patients ideas as to how they can help campaign effectively!
Wide ranging, interesting, intelligent and postiive for people with ME
some great interview that break down long standing issues and update on recent ones. interviewees from different places and and areas of work including scientists, campaigners, politicians and patients
very enjoyable and useful