Petition to support Dr Myhill’s complaint to the GMC

As was previously reported by #MEAction, Dr Sarah Myhill has made a formal complaint to the General Medical Council (GMC) about the authors of the PACE trial.
In addition to asking people to write to the Chairman of the GMC, she has now set up an online petition which people can sign if they wish to support the complaint:
https://www.change.org/p/the-general-medical-council-i-am-showing-my-support-for-dr-myhill-s-complaint-to-the-gmc-about-the-pace-authors
The petition is open to all UK and non UK citizens.
The PACE trial was a deeply flawed study which has resulted in harm to ME patients around the world due to the negative impact it has had on prescribed treatments, research, services and attitudes. If you would like the GMC to investigate the conduct of the PACE trial authors please consider signing the petition and/or writing to the GMC.
More information about Dr Myhill’s complaint is available from her website:
http://www.drmyhill.co.uk/wiki/My_Complaint_to_the_GMC_about_the_PACE_authors

Facebook
Twitter
WhatsApp
Email

Latest News

redish square image with the US Capitol photo with a red overlay on top of it. The words Congress is hearing from us. Then the MEAction logo in the center bottom.

#MEAction: Congress Is Hearing from Us

#MEAction has been hard at work connecting individuals to their elected officials to talk about the ME/CFS Research Roadmap, Medicaid, and telehealth.  We’ve been partnering with #NotJustFatigue on setting up congressional meetings in order to ask our elected officials for their support in making funding of the ME/CFS Research Roadmap a reality. #MEAction State Chapter

Read More »
blackish rectangle with the words, MEAction Georgia Volunteer - Maggie Boxey- at TEDxOjia with the meaction logo in the bottom right corner.

#MEAction Georgia Volunteer, Maggie Boxey, Speaks at TEDxOjai

#MEAction Georgia recently had a huge accomplishment. Maggie Boxey, who is a member of the Georgia State Chapter, a Navy veteran, and a published author, recently gave a Tedx talk about her experience as a person with ME. Maggie was diagnosed a year ago but has been sick since 2020. Before becoming sick Maggie and

Read More »

SOS: Save our Science

People disabled by ME and Long Covid across the UK send out an SOS.  It’s time to send out our SOS signal, if we want to have funded research. May 12th is Myalgic Encephalomyelitis Awareness Day. On this day, the #MillionsMissing with myalgic encephalomyelitis (ME) gather to demand an increase in research and care for

Read More »