The UK CFS/ME Research Collaborative to livestream AGM on 27 April

The 2016 Annual General Meeting of the UK CFS/ME Research Collaborative (CMRC) will be livestreamed on Wednesday 27 April, from 2.45 pm to 3.30 pm British Summer Time. Viewers must preregister.
The agenda of the AGM is as follows:

  • Welcome and apologies
  • Annual report 2014-15
  • Charter revisions/approval
  • Plans for 2015-16
  • Membership of the Board
  • Any other business

The CMRC was set up in 2013 to provide a mechanism for ME/CFS charities, researchers and clinicians to work together, especially to attract new funding to the field. The organisation’s launch proved controversial because the Collaborative included not only biomedical scientists but members of the biopsychosocial school of psychiatry responsible for studies such as the PACE trial.
However, its conferences have proved to have a substantial biomedical focus and the CMRC recently launched its Grand Challenge — a biomedical project consisting of a national UK ME/CFS genomics study planned to include more than 10,000 biological samples. The group has also started to attract new scientists to the field, including the internationally known epidemiologist Professor George Davey Smith.
Further information about the CMRC and its upcoming activities, including the 2016 conference and the Grand Challenge, can be found here.
 

Facebook
Twitter
WhatsApp
Email

2 thoughts on “The UK CFS/ME Research Collaborative to livestream AGM on 27 April”

  1. Rebecca, you’re misinformed.
    CMRC do not fund Peter White. They don’t and can’t because they don’t allocate funds to anyone. That is not their purpose.
    At the link that you yourself gave it states:
    “Action for M.E. took over the management of this study in July 2014, following the closure of the CFS Research Foundation, which had already secured and allocated funding for it.”

Comments are closed.

Latest News

greyish rectangle image with the words: #MEAction is Excited to Announce: Pillow Writers Anthology Issue 1: Near-Life Experiences. In a small grey square the words Get Your Copy Today! with a black line underneath. On the right hand side of the square is the image of the book cover that has a water color of flowers. the #meaction logo is at the bottom of the image.

Pillow Writers Anthology, Issue 1: Near-Life Experiences Available Now!

The Pillow Writers Anthology, Issue 1: Near- Life Experiences is a new literary magazine in the disability community. This inaugural issue features poems, stories, and essays by 17 writers who call themselves the Pillow Writers. The Pillow Writers are an international group of writers living with the neuro-immune diseases of myalgic encephalomyelitis (ME) and Long

Read More »

#MEAction UK’s email/letter to Andrew Gwynne MP

To: Andrew Gwynne, Under Secretary of State for Public Health and Prevention Subject: Treatment of Very Severe ME  email [email protected] Dear Andrew Gwynne,  Thank you for being an ally to people with ME  (myalgic encephalomyelitis) and Long Covid and committing to ensuring publication of the DHSC ME/CFS Delivery Plan without more delay.  We trust your

Read More »
Scroll to Top