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On this basis the people making money out of CBT should be pumping money into ME charities that support it :whistle:

I’m hearing that people in my area are being offered GET through the reorganised NHS Service which is community based alongside pain service as opposed to previous hospital based (no doctor involved) service which had moved to a PACE lite management programme approach. Seems the reorganisation...

It’s so difficult to know if a supplement is making any difference to me. I think I’m fairly sure magnesium helps as I’ve run out a couple of times and not realised and then after 2 or 3 days wondered why I was aching more. But changes could be for many other reasons related to activity levels...

Maybe ask if you can try nortryptiline it’s supposed to be less of a sedative hangover.

im copying a tweet from Alzheimer’s Research UK who are campaigning for 1% of the cost to the U.K. economy of dementia to be spent on dementia research currently it stands at 0.3%. They did a petition and got a minor celebrity to present it at Downing Street. The point I want to make is that...

Sticking my nose in here but I had a look at the ANMES site info under what is ME. In my opinion it isn’t frank enough about prognosis. It is possible to give out a more realistic message as shown by ME Association content on this issue...

@chicaguapa did you tell her the Guardian doesn’t generally run anything without at least a tinge of BPS ideology

Saw it on ME Association very sad

Hell yes

Meant Claire Fox not chronic fatigue

Trying to not be party political just highlighting that CF is all over the BBC in the last few days.

I’m not in US though so probably best for someone from there to pick up

If the only input is presubmitted questions what’s the point of using this “meeting” format it might as well or more accessibly for people with ME be done as blog from Unger and guest blogs.

Interesting this has copies of all the letters to the schools and consent information @dave30th so some of them know they should be providing this

Credit to the Mail again for publishing a good article on ME and to ME Association patients and Merryns family for working with them on this.

A new level of tripeness

Ah ok didn’t realise they sweeten it should have thought

Tried almond milk in a decaf latte during MM never had almond milk before it was very sweet.

:rofl::rofl::rofl::rofl::rofl: I’d rather have M&S logic tho

The Chalder effect