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...
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...
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.
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