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I would definitely raise it with GP. If it gets worse & if any swelling.

‘Many people with ME’ when referring to a two digit figure strikes me as hyperbole.

Going by posts I’ve seen on social media there are people with ME who work or study part time but are not able to do any cleaning or food preparation or any social activity at all relying on support from formal or informal carers for the daily living necessities. If the descriptors assume a...

Hoping some of the sensible researchers and health professionals will join in on this.

Good to see the ME Biobank & Dr W are looking at post covid research.

Shower - I think you could specify full shower standing up or sitting down

Clown factory scamming a living - nauseating

Never heard of cabin syndrome - ever i have heard of cabin fever - you know, the one where you get so cheesed off with being inside the same four walls Another scam - how do these people get public funds to churn out such utter tripe

Can’t see any mention of who the grant is coming from which seems unusual.

Twitter at least has an element of monitoring when I’ve reported stuff on there they occasionally take action. On Facebook nothing I’ve ever reported has been deemed to be outside even their low standards theres such a mix you really do have to look behind anything to see as best you can if...

So the behavioural treatment CBT helps (allegedly) so the problem must be behavioural. all those health charities welcoming CBT as psychological support for their diseases be careful what you wish for - psychosomatic Trojan horse.

TRIPE barrels full of the stuff

Great stuff by @Brian Hughes love you brought Father Ted into your blog :thumbup:

Brilliant work @Michiel Tack you totally shredded their shoddy workmanship.

So if they’re so similar is there really any point in having something called Qfever fatigue syndrome?

Reduce Chalder research certainly

Agree - I think it would be practice nurse role for regular reviews. And making those appointments 20 minutes instead of 10 so the nurse could have a chat and bring in the messages and build up a relationship with the patients would be more effective.

From my brief skim it would appear that people who have diabetes and have had leg ulcers are to be actively encouraged to monitor their physical symptoms and to seek help.

Hope it goes well I see there’s a State level politician due to take part as well which seems positive.

Our guidelines and in particular the communication of them has been a complete mess since February.