In our final episode we discuss severe ME. One in four people with Myalgic Encephalomyelitis (ME) are severely or very severely affected. Our guests for this episode are Dr Robin Kerr, a GP with over 10 years’ experience in general practice; and patient advocate Helen Brownlie, who campaigns on severe ME through the UK charity which specifically supports people with severe ME, the 25% ME Group. To represent the voice of people living with severe ME, who are too unwell to speak for...
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In our final episode we discuss severe ME. One in four people with Myalgic Encephalomyelitis (ME) are severely or very severely affected. Our guests for this episode are Dr Robin Kerr, a GP with over 10 years’ experience in general practice; and patient advocate Helen Brownlie, who campaigns on severe ME through the UK charity which specifically supports people with severe ME, the 25% ME Group. To represent the voice of people living with severe ME, who are too unwell to speak for...
Episode 3 - Learn About M.E. and the new NICE Guideline
Learn about ME
28 minutes
3 years ago
Episode 3 - Learn About M.E. and the new NICE Guideline
In this third episode of our Learn about ME podcast series, we hear from, Dr Nina Muirhead, creator of the Learn about ME CPD learning module and, Dr Gregor Purdie, about the importance of highlighting the changes in the newly updated NICE guideline on ME/CFS: diagnosis and management. They are joined by, Helen, who lives with ME and who volunteers for The 25% ME group. Helen shares her experience in order to encourage healthcare professionals to implement the changes in the guideline. We hop...
Learn about ME
In our final episode we discuss severe ME. One in four people with Myalgic Encephalomyelitis (ME) are severely or very severely affected. Our guests for this episode are Dr Robin Kerr, a GP with over 10 years’ experience in general practice; and patient advocate Helen Brownlie, who campaigns on severe ME through the UK charity which specifically supports people with severe ME, the 25% ME Group. To represent the voice of people living with severe ME, who are too unwell to speak for...
