People disabled by ME and Long Covid across the UK send out an SOS. It’s time to send out our SOS signal, if we want to have funded research. May 12th, is Myalgic Encephalomyelitis Awareness Day. On this day, the #MillionsMissing of people with myalgic encephalomyelitis (ME) gather to demand an increase in research and
Following another busy and productive year, #MEAction Scotland is publishing our 2024 Impact Statement today, which covers the 2024 calendar year. It reports on our work to campaign for effective support, create stronger advocates and raise awareness. The statement brings together some key successes over the year. Some highlights include: The work continues towards a
In Judith Woods’ Comment piece on 2nd February 2024, ‘28-year-old Lauren Hoeve died by euthanasia – to a degree, I understand her pain’ she boldly asserts that a great deal of Lauren’s anguish was ‘psychological’. The writer then belittles the immense pain suffered by people with severe ME, as Lauren did from 2019, as she
