Hopefully @dave30th will agree and use what you’ve done. Then you can claim an assist as they call it in sport these days when you set up the other player to score a goal
Who is he @Leila and do you know if he has any knowledge of ME? Maybe if you’re a regular follower of his and you can manage it you could message him links to the MEAssociation?
Thanks for sharing your experience @vsou. Unfortunately with the snowball effect that happens around improvement stories and recovery stories. Information about people who have had negative effects and or no improvement often seems to be overlooked and ignored.
Well you never know if they’ve got any common sense at all it’s possible that with Long Covid in the news they might have had a lightbulb moment and thought the course might be useful.
Posts about the NHS England announcement about Long Covid clinics have been moved to this thread
https://www.s4me.info/threads/uk-nhs-england-online-tool-and-clinics-for-long-covid.15790/
Liaison psychiatry teams all round the country no doubt offering their services....... i hope there’s going to be some some actual testing and medical treatment. Definitely will be interesting to see how this turns out in practice.
I get out of breath very quickly if I have to walk uphill or stairs. I always put it down to being overweight but I can go a lot further on the level without gasping. I think I’ve always been a shallow breather and was absolutely hopeless at cross country running at school - I had to resort to...
Moderator note: Please be mindful of Rule 12 - No non-ME politics.
Posts stating facts about President Trump will be allowed, but please avoid making any comments that could be seen as political. The thread has been reviewed and some breaches have been identified and dealt with.
Thanks @ladycatlover i will do that eventually
just don’t have the brain capacity to tackle it until my refurbishment project is finished. There’s so much physical and cognitive energy needed for decision making and moving stuff around in the house.
you might need to remind me next summer...
Excellent thread @Snow Leopard. I have things I would love to be spending my time on. I have some milder ME days when I can manage to do a lot more than on my worst moderate ME days. In theory I could do some stuff that would improve my quality of life I’m not even thinking at a wish list...
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