More fantastic news from @BethDobbin. She has 360 sports people supporting her call for fair funding for ME research. We join her call for fair funding alongside camapaigning for NHS services for the very severe.
@BethDobbin You can help by contacting your MP and asking them to demand services for the very severely ill and fair funding using the guides in the article here: https://t.co/GuQ8mNuHjT
As always, only take action if you
Eleanor Hayward writes in @thetimeses about how @BethDobbin went from being an Olympian to bedbound for 22 hours a day. Beth is open about her grief at losing her athletic career.
https://t.co/BcP2C1ldu4
@BethDobbin You can help by contacting your MP and asking them to demand services for the very severely ill and fair funding using the guides in the article below: https://t.co/GuQ8mNuHjT.
This was only possible due to the hard work and dedication of our volunteers, Helen and Pam and our trustee Janet alongside Avril from Action for ME. Our thanks to everyone who took part.
#MyalgicEncephalomyelitis#pwME#RCGPAC#RCGPAC26
During the two days of the Royal College of General Practitioners conference MEAction UK and Action for ME engaged with well over 200 GPs and trainee GPs and most were very keen to learn more about how to support their ME patients.
Today, at #RCGPAC26 MEAction UK were pleased to meet a representative of the Lyme Resource Centre - Scotland The MEAction UK & Action for ME stand has been busy with our volunteers working hard to answer questions & hand out information.
#MyalgicEncephalomyelitis
MEAction UK are at the #RCGP conference in Glasgow with Action for ME.
We’re here to tell delegates about #LearnAboutME & how to support #pwme. We’ve already engaged with GPs, registrars, medical students & pharmacists with positive reactions.
#MyalgicEncephalomyelitis
MEAction UK has its own mailing list. Sign up for a closer look at our work in England, Scotland and Wales, including campaigns, updates and information. https://t.co/jCJqtWvAC0
#MECFS#LongCovid#MillionsMissing
Thanks to @bethdobbin for speaking about her illness to raise awareness, even at the cost of her own health and for describing the impact of ME so vividly. Beth is bed bound for 22 hours a day. We know how isolating this is so want her to know that she is not alone.
Share & help this go viral!
George Monbiot writes about the 'astonishing, ongoing mistreatment of people with #ME/CFS.'
https://t.co/Nv2oyrMzg7
#MyalgicEncephalomyelitis
https://t.co/B62veBcwwC
Update - Please read this petition about Karen Gordon and sign if you haven't already. Be aware that Karen is still very ill and having a hard time in hospital, so read with caution.
https://t.co/rOQakOtAkS
#VerySevereME