We have an update from Karen's family. Karen is severely ill and being threatened with legal action if she doesn't move to a hospital unit with a strong psychiatric approach. Please sign and share her petition.

ow.ly/VRyH50RcpuG

#MyalgicEncephalomyelitis #VerySevereME

Joanna Bruce The Real M.E. 👩‍🦽🦥♿️🏴󠁧󠁢󠁳󠁣󠁴󠁿📢, #MEAction Scotland volunteer, was interviewed on Channel 4 News tonight & talked movingly of the need for more ME research & her involvement in the groundbreaking DecodeME the ME/CFS Study. Thank you Jo.

ow.ly/UFEh50R8LgQ

Read Ellie Fry report on Millie's fears that she may die in hospital in The Mirror. #MEAction UK is quoted urging the hospital to listen to ME experts stop inappropriate treatment.

ow.ly/El7A50R8Cfc

#SevereME #pwME

Heartbreaking Millie update 💔:

Petition
ow.ly/FQpn50QUWUq

Fundraiser
ow.ly/ySTl50QUWUp

#SevereME #MilliesevereME #pwME

Excellent article George Monbiot The Guardian on the national scandal of treatment of #pwME . This is happening now - Millie & Karen are both at risk of starvation in NHS hospitals.
ow.ly/femI50QHstC
ow.ly/u0iv50QHstB

ow.ly/tgPc50QQYxZ

#MyalgicEncephalomyelitis

Great work #MEAction Scotland on this article in the Nursing Times.

'The charity ME Action Scotland has spotlighted the need for health boards across the country to invest in ME/CFS services ...'

ow.ly/tISJ50QMQM3

#MyalgicEncephalomyelitis #VerySevereME

Update about Karen’s hospital stay from her family.

ow.ly/Z0PW50QKibv

Please continue to tell people about this petition and continue to share it on-line.

#MyalgicEncephalomyelitis #VerySevereME

Good news. #MEAction 's Modified Movement Class is now available free on video.

#MEAction was delighted to partner with Nourish Therapeutic Yoga to bring you this new offering & it is in such demand that we will be bringing you a new class each quarter. ow.ly/Ss3450QJRzm

UPDATE FROM MILLIE'S PETITION

The NICE guidelines have now been read by the hospital and the staff are trying to follow them.

Read more here:
ow.ly/H2wL50QJPRy

#MyalgicEncephalomyelitis #VerySevereME

Millie has won her appeal & is no longer sectioned after Dr Weir saw her & wrote to the tribunal in support. Millie still can't return home, she needs a PEG for nutrition, which they refuse.

Please sign & share.
ow.ly/xKYa50QIj44

#MyalgicEncephalomyelitis #VerySevereME

Some very good news about Millie.

MILLIE UPDATE BELOW

Please keep signing and sharing the petitions for Millie and Karen.

ow.ly/iY6L50QIbZF

ow.ly/BV7u50QIbZE

#MyalgicEncephalomyelitis #VerySevereME

Stoo Brown, an #MEAction Scotland volunteer, was interviewed by The Sunday Post about the lack of medical care for people with ME in Scotland.

ow.ly/qvoA50QHLwM

#MyalgicEncephalomyelitis

Please take some time out of your weekend to sign and share these petitions to stop the medical mistreatment of Karen and Millie.

ow.ly/femI50QHstC

ow.ly/u0iv50QHstB

#MyalgicEncephalomyelitis #VerySevereME