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Medical Education Webinar: Myalgic Encephalomyelitis - Diagnosis, Management and Current Research
- Thread starter Arnie Pye
- Start date
approx 1 hour 15 minutes
The webinar is aimed at doctors
Moderated by Dr Teresa Clark - a physician of a 'complex chronic diseases programme'
Dr Nina Muirhead
Her illness has become less severe, so she is able to work part-time now - good to hear
Nina uses the 'complex' descriptor of ME - I do wish our advocates wouldn't use that word.
Prognosis of 5% recovery is mentioned - I think it would be useful to explain that many people recover from the symptoms before the 6 months mark.
Covers symptoms in a comprehensive way, emphasises the seriousness;
Dismisses the idea that it's depression or deconditioning
Covers CCC and IOM diagnostic criteria, and overlap with Long Covid symptom pattern
The comment 'Be proactive about making a diagnosis - but keep looking for other diagnoses' was good
Disappointing to see unevidenced treatments included in the list of treatments such as Low Dose Naltrexone and B12, even though the heading on the slide is 'Conservative, pharmacological'. Mention of mast cell treatment - maybe there's something in that, I don't know, but it is unevidenced, and I think that should be said.
Forthcoming paper on the quality of life on patients and their family members. Impact on ME/CFS and Long Covid family members worse than in cancer.
Dr Lucinda Bateman (starts around 20 min mark)
Taking a break. I think this is shaping up to be a useful webinar for medical professionals. Nina's presentation was helpful, and Lucinda is a very clear presenter on ME/CFS.
The webinar is aimed at doctors
Moderated by Dr Teresa Clark - a physician of a 'complex chronic diseases programme'
Dr Nina Muirhead
Her illness has become less severe, so she is able to work part-time now - good to hear
Nina uses the 'complex' descriptor of ME - I do wish our advocates wouldn't use that word.
Prognosis of 5% recovery is mentioned - I think it would be useful to explain that many people recover from the symptoms before the 6 months mark.
Covers symptoms in a comprehensive way, emphasises the seriousness;
Dismisses the idea that it's depression or deconditioning
Covers CCC and IOM diagnostic criteria, and overlap with Long Covid symptom pattern
The comment 'Be proactive about making a diagnosis - but keep looking for other diagnoses' was good
Disappointing to see unevidenced treatments included in the list of treatments such as Low Dose Naltrexone and B12, even though the heading on the slide is 'Conservative, pharmacological'. Mention of mast cell treatment - maybe there's something in that, I don't know, but it is unevidenced, and I think that should be said.
Forthcoming paper on the quality of life on patients and their family members. Impact on ME/CFS and Long Covid family members worse than in cancer.
Dr Lucinda Bateman (starts around 20 min mark)
Taking a break. I think this is shaping up to be a useful webinar for medical professionals. Nina's presentation was helpful, and Lucinda is a very clear presenter on ME/CFS.
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