Esther Cole

Let's talk about M.E/CFS

[Esther Cole @esthercole]

https://t.co/giqnplyL2t

[DecodeME the ME/CFS Study @DecodeMEstudy]

There’s still time to participate in Action for ME’s Big Survey!

To take part and find out more, head to Action for ME’s website: https://t.co/iF0mi45xIh

Thank you for supporting ME/CFS research.

[TopShagger @Plentyshit]

If only 👑

[ThePOTSPostman @ThePOTSPostman]

I absolutely love this video by @Dysautonomia

It gives such a great explanation of what POTS is!

If you haven’t seen it, please give it a watch and let me know what you think!

[Esther Cole @esthercole]

@realmartinkemp That’s lovely Martin what a nice chap you are:)
MerryChristmas

[Esther Cole @esthercole]

https://t.co/3IczWgClAL

[Esther Cole @esthercole]

@Fern_Britton What a little love ❤️ I

[Esther Cole @esthercole]

@theJeremyVine Thank God for that🙌🏻🙌🏻

[Esther Cole @esthercole]

@ChrisLangWriter @jlpartnership That’s good to hear Chris I hope he enjoyed it:)

[Esther Cole @esthercole]

@jamesmartinchef It was really lovely to see Brian on the show, he may have been poorly but he’s looking good.Wishing you good health Brian.X

[Esther Cole @esthercole]

@mrmichaelball I’ve just received a calendar with your lovely face all over it😊

[Eric Topol @EricTopol]

Myalgic encephalomyelitis was first recorded in 1934 in Los Angeles after an outbreak of atypical polio. It has taken nearly a century and #LongCovid to "get needed attention"
https://t.co/ryyI15mfnf @NanetteAsimov #mecfs

[DecodeME the ME/CFS Study @DecodeMEstudy]

We're excited to announce that #DecodeME is ready to fully launch in SEPTEMBER!

If you’ve signed up for emails, we’ll email you when we open recruitment.

Register for updates here https://t.co/cNbuaaeHky

#pwME #MECFS #decodemestudy #biomedicalresearch

[Esther Cole @esthercole]

@Fern_Britton How are you feeling with it Fern?x

[Esther Cole @esthercole]

@RealTimVine With 7up Tim it’s a game changer:)

[Esther Cole @esthercole]

Wow to finally hear ME being spoken about and taken seriously gives me such hope for the future.Please make it happen @sajidjavid

[Sonya Chowdhury @SonyaChowdhury]

Great to be able to participate in @sajidjavid @LucyChappell2 #MyalgicEncephalomyelitis research on @PSPforMECFS and wider research. Important that we now engage wider through research working grp to inform cross-gov delivery plan @actionforme @DocStrain @CGATist

[Sajid Javid @sajidjavid]

Yesterday I spoke at the launch of the APPG on ME's new report.

We must improve the lives of people with ME - I’ve seen the devastating impact it can have.

For too long it hasn’t received enough attention which is why I will develop a cross-govt plan to improve outcomes.

[The Times and Sunday Times @thetimes]

My daughter couldn’t be saved but there’s hope for other ME patients https://t.co/bpgfgg6ogW

[Open Medicine Foundation @OpenMedF]

$8 Million Clinical Trial of a Mitochondrial Booster Underway in #MECFS! Read the new article from Health Rising by @CortJohnson: https://t.co/5E8XHpEng5

[Esther Cole @esthercole]

@BBCAlagiah @BBCNews Happy to see you back George you look great:)x