Tom Kindlon#ThereForMe Guest post from Tessa Munt MP
https://www.thereforme.uk/p/the-case-for-change-for-people-with
Screenshot from Science for ME weekly update
#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
@mecfs
Eleanor Fielding#ThereForME
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#ME #Chronicillness #LC
#PEM #POTS #LivesWeCannotLive
#MissingMillions
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(UK) “Six months since the publication of the Final Delivery Plan for ME” blog post by by #ThereForME
Links:
https://www.thereforme.uk/p/campaign-update-30-six-months-since
Screenshot from latest Science for ME weekly update
#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
@mecfs
(UK)
#ThereForME co-founder Karen Hargrave writes about applying for Continuing Healthcare funding
https://www.thereforme.uk/p/why-is-continuing-healthcare-funding
Screenshot from latest Science for ME weekly update
#SevereME #SevereMECFS
#SevereCFS #VerySevereME
#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
@mecfs
A cartoon for anyone who has been disbelieved, and how that disbelief affects the whole of our lives.
#ThereForME
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#ME #Chronicillness #LC
#PEM #POTS #LivesWeCannotLive
#MissingMillions
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Trying to book an accessible holiday is marginally less difficult than trying to buy a new car and a new wheelchair at the same time!
#ThereForME
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#ME #Chronicillness #LC
#PEM
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#ThereForME
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#ME #Chronicillness #LC
#PEM #POTS #LivesWeCannotLive
#MissingMillions
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Another week, another opportunity for psychiatry to recognise #ME as a serious post-viral illness
#ThereForME
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#ME #LongCovid #Lyme #POTS #PEM
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Yet another week of medical negligence looms into view promising confusion+despair for millions
#ThereForME
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#ME #LongCovid #POTS #PEM
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#Justice4ME
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From David Tuller @david
I spoke with Oonagh Cousins, one of the people involved in #ThereForME, about the UK government's pathetic so-called "delivery plan" for ME and about the great disappointment many are feeling about it:
