Independent: Time for Unrest: Why patients with ME are demanding justice | 07 January 2018
A new film sheds light on a condition that is largely ignored. Nathalie Wright reports on the struggles patients face to be taken seriously by doctors.
A new film sheds light on a condition that is largely ignored. Nathalie Wright reports on the struggles patients face to be taken seriously by doctors.
“I was fit, I went rambling and went to the gym,” she said. “But ME has taken my whole life and any fulfilment I might have had.”
Nature News Feature: A reboot for chronic fatigue syndrome research | 04 January 2018 Read More »
This is an excellent feature article that focuses on the developing research situation in America, but also includes items relevant to the situation here in the UK.
We believe it is important to obtain regular feedback from people with M.E. as to what they regard as the most important priorities for UK research.
Peeblesshire News: Peebles gives Phoebe her perfect present | 02 January 2018 Read More »
In October we reported how Phoebe Boag had reached out to locals to raise funds for an electric wheelchair, having been housebound for two years.
A recent scientific trial has led to acrimonious debates over chronic fatigue syndrome, aka ME, and boosted interest in a secretive therapy that some call a “cult” and others call a “miracle”.