@jamesmurray_ldn We need the immediate setting up of NHS specialised care to prevent more suffering and deaths.
Stop the harm, Stop the deaths, Start the service.
Lobby your MP!
Read more and watch the video here: https://t.co/qBqaVnKLAn
#MillionsMissing#VerySevereME
Lighting up the darkness for ME.
#MEAction UK took to the streets of London to urge @jamesmurray_ldn, the Secretary of State for Health and Social Care, to listen to the most severely ill people with ME.
Last night, #MEAction UK took to the streets of London to @jamesmurray_ldn to listen to the most severely ill people with ME & set up NHS care.
Lobby your MP! https://t.co/6G49HavwGJ
More locations, photographs and videos coming soon!
#MillionsMissing
You can learn more about the module and the complementary resources here ๐๐ผ
https://t.co/wJhYdwa4fi
The thirteenth Learn about ME podcast is coming soon!
#MyalgicEncephalomyelitis#MyalgicE#HealthEducation
Learnaโs free, highly rated, CPD-accredited module on ME, available for GPs and
healthcare professionals, has been updated to reflect evolving biomedical
understanding of ME.
Please share! We have asked you to contact your MP using our advocacy guides (link to our full guide https://t.co/p1tXGFjwBj or to our shorter guide here https://t.co/xYk46J1tex). This is showing results so please keep doing it if your energy allows..
@jamesmurray_ldn LinkedIn @james-murray-6616a0122
Your MP should have their own social media accounts. Could you find and save the tags as we will be posting more images to share over the next few weeks?
Liz Jarvis, Liberal Democrat MP for Eastleigh asked question below. Ther response is there is still no plan for the very severe . They have to stop the harm, stop the deaths, start the service for the #MillionsMissing now!
Thanks to TheyWorkForYou.
https://t.co/jxrYQik9mS
#ThereForME co-founder, Karen Hargrave, speaks very powerfully to @theipaper about the financial costs of caring for someone with very severe ME, the lack of help available and the stress and anxiety this causes.
#MyalgicEncephalomyelitis#HealthEquality
https://t.co/OPKUWXNHII
Listen to Emma Barnett's interview with former Team GB rower and #ThereForME team member, Oonagh Cousins about her experience of living with ME following Long Covid
https://t.co/hKbZo1pS0t
Since retiring from elite sport at the end of 2022, she has focused her efforts in the Long Covid and ME space โ working at the charity Long Covid Support, as part of a social science research team at the University of Oxford, and in the #ThereForME team.
Please share!
We have asked you to contact your MP using our advocacy guides (link to our full guide https://t.co/p1tXGFjwBj or to our shorter guide here https://t.co/xYk46J1tex). This is showing results so please keep doing it if your energy allows..
@jamesmurray_ldn LinkedIn @james-murray-6616a0122
Your MP should have their own social media accounts. Could you find and save the tags as we will be posting more images to share over the next few weeks?