If anyone was still giving PG the benefit of the doubt......
on the positive side it’s a letter not an article
eta note the specific wording about no harm shown in trials rather than arguing GET doesn’t cause harm so they have conceded that wider point
https://www.s4me.info/threads/bacme-position-paper-on-the-management-of-myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-oct-2020.17360/page-8#post-331057
document posted here
You’re having a positive week @lunarainbows due to all the excellent work you’ve been doing on advocating for your needs. Virtual pat on the back and hug from me :thumbup::hug:
My view on coffee or stimulants generally is informed by my experience. I managed to push myself to keep working for probably 5 years by having expresso coffee from the canteen at work or train stations when travelling. I felt pretty terrible but the coffee made me high enough to push...
INews article about digital approach to treating LC being introduced in some areas of U.K.
https://inews.co.uk/news/science/long-covid-digital-treatment-programme-rolled-out-in-hospitals-to-help-patients-with-chronic-illness-900691
made me think of Gulliver’s Travels where the little people on the island who crack the pointier end of the boiled egg before they eat it think they are completely different to the little people who crack the rounder end first
Wondering if this is something that the House of Commons Select Committee on Science might be interested in bearing in mind Carol Monaghan is on that committee. @Caroline Struthers
Great news. I hope people in the community who are able to will support Keith as with Dave he has done a lot towards highlighting the issues and I feel it is important for his work to continue without having to be reliant on sporadic grants.
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