We've added more information about our new book to our website, including answers to some frequently asked questions. 👇👇.

RT @ClagueNjc36: Just saw this in the physio frontline journal! All advocacy is important however small! Thanks @thecsp @PhysiosForME https….

RT @memhj: ‼️Michelle Bull @MichelleBull4 @PhysiosForME.Living with ME/CFS and Long Covid: Managing symptoms.Norsk tekst. Evening lecture #….

For fun, here's some strange facts about us - can you guess who's who?!. One of us is an avid player of lawn bowls.One of us attends a punk/rock festival annually.One of us has published four horror novels.One of us goes to France every year to cycle up mountains (slowly)

It's our six year anniversary!. To celebrate, the four of us spent a lovely weekend together, plotting and planning what our seventh year will look like. You can read a whole recap of our year in our latest blog post here.

RT @ClagueNjc36: Well that's a wrap. 40 follow-up measurements (across Liverpool and Manchester) completed for our #tvns study. Thank you t….

RT @bendymarsh: Every morning.Every crash.Every small win.Every friend let down.Every dismissal or disbelief.Every medicine or therapy that….

Released this month is a German language version of our book "A physiotherapist's guide to understanding and managing ME/CFS". We had no input on cover or translation choices, but are pleased our key messaging has broadened its reach .

RT @ClagueNjc36: Pleased to have 3 abstracts accepted for the Chartered Society of Physiotherapy conference in Nov. Thanks @thecsp @Physios….

RT @PressAwardsuk: Congratulations to "M.E. Awareness and Reform" from @thetimes for being awarded winner of Campaign of the Year at The Pr….

RT @VirusesImmunity: Published today! Victoria Bastos, @KerrieGreene_ et al found two distinct immunotypes of ME/CFS based on the cerebrosp….

RT @TomKindlon: "Mason Foundation awards $1.44 million to fight [ME/CFS]". Great to see this significant funding f….

RT @SarahLizzyLou: Now I’ve settled at my in-laws’ place in SE England, I want to get an official ME diagnosis. Have been looking at the lo….

RT @TimesONeill: Last year, following the inquest into my daughter's death from ME a minister said the govt was “committed to funding high….

Finally, on #MEAwarenessDay we'd like to emphasize the importance of learning about ME to physiotherapists and other healthcare professionals. And to #pwME we'd like to offer our continued support and let you know that you have a dedicated team on your side 💜.

And of course here's some information about our book, which provides more detailed evidence based material to help you understand more about safe management of people with ME. #MEAwarenessDay .

Here are seven slides that give a basic overview of ME and relevant issues for health professionals . #MEAwarenessDay .

Here is a one page handout to help identify areas of any practice that might need to be adapted to work safely with people with ME. #MEAwarenessDay.

On #MEAwarenessDay we encourage all physiotherapists and other allied health professionals to take a moment to learn about this condition, as it is relevant no matter what speciality you work in. We have some resources to help. @thecsp @theRCOT.

Today is #MEAwarenessDay . We've published a blog with some updates of our recent activities.

RT @ThereForME_UK: On #WorldMEDay the UK ME community faces a twofold threat: the loss of critical welfare benefits, and a lack of meaningf….