From various tweets it seems Dr Weir has said that with IV Saline and nutrition, most patients recover to where their life isn’t threatened.
Paul Keeble is also back on twitter “Dr Weir is seeing patients as unwell as Maeve about every 6 months” “Feeding in the community. NG then...
But a “regular person” wouldn’t be expected to understand ATP or biochemistry or research specs. I think if the Daily Mail and Co were saying...
Good reply there.
It was 2021, I’d say Covid was at its worst the year before in March 2020
I think I’d do a leading introduction “It was said at a recent Coroner’s Inquiry that there is no specialist service for severe ME in the NHS....
This telegraph piece is excellent Link if you can’t use the paywalled one above https://archive.ph/fRT5B
I believe in his evidence he said pwS/VS ME get a side room with black out curtains automatically plus there has been specific S/VS ME training...
Apparently starts at 9.30am tomorrow
From written evidence, GP Dr Shenton “I don’t believe I can put ME on the death certificate because many of the Drs involved do not believe ME is...
No time for Dr Weir today, he will be up tomorrow morning.
P Keeble is crashing so won’t report much more today (hardly surprising this would take a toll on anyone) [ATTACH] “Maeve asked about contingency...
Yup, the picture of different people making different decisions, or not making decisions, is building. We’re getting some idea of the “passed from...
“Not sure if the press is here today but some firecrackers towards the NHS about lack of provision” “Sarah Boothby commenting on various...
This one isn’t very clear. Dr Strain was seen as the lead but has no nutrition knowledge Psych said it isn’t a terminal condition [ATTACH]
There are still Drs all over the NHS who think it’s psychological and Dr Strain has had frank conversations with them [ATTACH]
TPN would only be offered if she was sectioned [ATTACH]
[ATTACH] [ATTACH] It seems Dr Strain is giving evidence this morning. He is a Consultant and also a Snr lecturer at Exeter Uni Medical School and...
That’s why I like the term “energy limiting condition” because it does explain (in a simplistic way) that we have energy, but it’s limited. That’s...
I think colloquially people say “chronic fatigue” because it’s shorter. They should be saying ME/CFS which is shorter still. I see the Daily a...
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