Public Talk by Dr Øystein Fluge and Bergen Team
Solving Complex Disease With High-Quality Biomedical Research and International Collaboration
We are pleased to announce that Dr Øystein Fluge and his team from Haukeland University Hospital in Bergen, Norway, will be giving a public lecture in Norwich on 26th January 2017.
Professor Simon Carding of University of East Anglia/Institute of Food Research will also be speaking.
Professor Carding is leading a team of ME researchers in Norwich - click here
The lecture will take place at The Assembly House, Norwich beginning at 18.30.
Dr Ingrid Rekeland and Kari Sørland from Haukeland University Hospital will also be present and presenting.
After the lectures a panel discussion will be held and questions can be accepted from the audience.
This is a wonderful chance to hear some of the top researchers of ME in the world
speaking of the work being carried out in Bergen, Norway and Norwich, UK.
Refreshments will be available.
The agenda is here -
The Assembly House is in the centre of Norwich, opposite the Millennium Library, and with good car parking possibilities and public transport links.
Here is the map reference - click here
The event is free but registration is required so please contact us.
If you would like to reserve a place then please use the contact form to request places or email to email@example.com with subject title Dr Øystein Fluge Public Talk.
If you would like to support to our research funds then links are available to be shared on the right of this page.
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See also Institute of Food Research article - http://www.ifr.ac.uk/news/events/2017/01/mecfs-biomedical-research/
Invest in ME Research is an independent UK charity finding, facilitating, and funding a strategy of biomedical research into Myalgic Encephalomyelitis (ME), and promoting better education about ME.
The charity's objectives are to initiate, maintain and augment a strategy of high-quality biomedical research into ME, to provide education about ME, and to raise awareness of the effects of the disease on patients and families.
The charity believes that biomedical research into ME is crucial in order to make progress in treating this disease. We also believe that education of healthcare staff, the media, government departments, patient groups and patients is to be a priority.
Invest in ME Research is run by volunteers - patients or parents of children with ME - with no paid staff.
Overheads are kept to a minimum to enable all funds raised to go to promoting education of, and facilitating and funding biomedical research into, ME.
We are a small charity but with supporters who have big hearts - and a determination to get the best possible research to be carried out to find the cause of myalgic encephalomyelitis and develop treatments.
We have links nationwide and also internationally.
Invest in ME Research is a founder member of the European ME Alliance (EMEA), a collaboration of European national charities and organisations.
The charity was also responsible for initiating the European ME Research Group (EMERG) concept, a collaboration of European researchers from major institutes.
The charity also has initiated the European ME Clinicians Council (EMECC), a network of European clinicians who will work together and share experiences of treating ME in order to establish better standards for patient care.
We do not receive, and have never received funding from government or government organisations.
The seriousness and urgency of the situation regarding ME makes it necessary for a charity such as Invest in ME Research to provide the impetus for funding biomedical research in order to provide hope for the development of diagnostic tests and remedial treatments.
The charity has pursued of policy of raising funds itself for biomedical research in order to fund research at top UK institutes. More information is available here.
We believe that clinicians should standardise on usage of the most up-to-date criteria which will be agreed and developed for diagnosis by the European ME Clinicians Council and European ME Research Group, along with international collaborators. in order that there is an agreed basis (noting that evolutionary improvement would be welcomed).
The charity organises an annual research Colloquium and conference regularly attracting delegates from 20 countries and funds research at the Quadram Institute and the University of East Anglia as well as influencing collaboration elsewhere, in UK, Europe and beyond.
Our conferences and colloquiums were organised from the beginning in order to provide a platform for research and a means of facilitating education about ME.
In order to bring the best education and research to bear on ME and to find and facilitate the best strategy of research into this disease the charity welcomes support for our work.
Our aim is to fund and facilitate research in order to establish an understanding of the aetiology, pathogenesis and epidemiology of ME. We hope this will lead to the development of a universal diagnostic test(s) that can confirm the presence of ME and, subsequently, medical treatments to cure or alleviate the effects of the illness
Our efforts are focused on setting up a UK/European Centre of Excellence for ME which will provide proper examinations and diagnosis for ME patients and a coordinated strategy of biomedical research into ME in order to find treatment(s) and cure(s).
Last Update 12/11/2016