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ME/CFS SOUTH AUSTRALIA INC

Registered Charity 3104

Email:
sacfs@sacfs.asn.au

Mailing address:

PO Box 322,
Modbury North,
South Australia 5092

Phone:
1300 128 339

Office Hours:
Monday - Friday,
10am - 4pm
(phone)

ME/CFS South Australia Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.

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ME/CFS South Australia Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.

Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.

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Invest in ME Conference 2010

Saturday 23 January 2010

Invest in ME Conference 2010Invest in ME will be hosting the 5th International ME/CFS Conference 2010 which will be held on Monday 24 May.

Here are the details:

The 5th Invest in ME International ME/CFS Conference 2010

A New Era in ME/CFS Research

This will be the fifth annual Invest in ME international biomedical conference on ME/CFS.

The conference will be held on 24th May 2010 in London and builds on the successful biomedical research conferences organised by Invest in ME in previous years.

As in previous years Invest in ME aim to raise awareness of the neurological illness myalgic encephalomyelitis (ME/CFS). We hope this conference will highlight the need for a national strategy for biomedical research which will lead to treatment and a cure for this devastating illness - an illness which is 5 times more common in the UK than HIV/AIDS - yet which has had comparatively little funding spent on biomedical research.

Why you should attend

The conference slogan is -

A New Era of ME/CFS Research

and the theme is

Education of healthcare staff in ME/CFS

With the recent discovery of the xenotropic murine leukemia virus-related virus (XMRV) retrovirus in patients with ME/CFS by the Whittemore-Peterson Institute, the US National Cancer Institute and the Cleveland Clinic of Ohio, we are witnessing a major breakthrough in the understanding and treatment of ME/CFS and in the implications in ME/CFS.

The education of healthcare staff about ME/CFS now needs to break with the past and reflect the new found knowledge about the pathogenesis of ME/CFS which high quality biomedical research is providing.

The conference will be oriented toward providing healthcare staff and others with knowledge of the latest research and the biomarkers which allow appropriate treatments to be prescribed.

The key to resolving, treating and curing ME/CFS lies in biomedical research.

Our 2008 conference in London focused on Sub Grouping and Treatments and showed indisputable proof from leading ME/CFS experts regarding the pathology of this illness.

Our 2009 conference concentrated on the severely-affected people with ME.

However, apart from a knowledge of the biomedical research which is ongoing it is necessary for healthcare staff to be aware of the multiple symptoms exhibited by ME patients and of the possible treatments available.

Research data and experiences of managing and treating ME/CFS will be presented as will findings from the latest biomedical research. The time is right for moving ahead with new findings.

The presenters at the conference represent the world's most current ME/CFS knowledgebase regarding ME/CFS.

The conference provides information and opportunities which are not available via the internet. One of the most important aspects at previous IiME conferences has been the creation or resumption of the unique networking opportunities available with some of the most renowned experts on ME/CFS in the world.

Who should attend?

The conference will appeal to healthcare professionals, doctors, nurses, paediatricians, occupational therapists, researchers, ME/CFS support groups, people with ME/CFS and those working in social services, educational support and the media.

The conference provides an opportunity for people within government, health departments, social services and education to be able to be informed of the true nature of ME/CFS and of the current status of diagnosis, treatment and current/future biomedical research possibilities.

Conference Registration

Registration will begin from 08.00 on 24th May.

Morning and afternoon refreshments, and a hot lunch will be included in the conference price.

A small quiet room adjacent to the lecture theatre will be available for some who may wish to rest.

The refreshment areas should be available as rest areas during the conference presentations. During lunch and breaks the lecture theatre should also provide a quiet area to sit and relax.

Please note this conference is a TICKET-ONLY event - tickets must be purchased prior to the event (please see our conference registration page).

Conference Venue

The conference venue is at One Birdcage Walk in the heart of Westminster, London. The conference will be held in the magnificent Lecture Theatre of One Birdcage Walk.

This wonderful venue will make the day a relaxing opportunity to network with other healthcare professionals and patient groups/charities.

CPD Accreditation

We hope that the conference will carry, as in previous years, the maximum 6 CPD points by the Royal Colleges.

Sponsorship

Invest in ME welcome sponsors for the 5th International ME/CFS Conference.

Please contact us here at the International ME/CFS Conference Email address.

See our current sponsors for the 5th International ME/CFS Conference - click here.

The above originally appeared here.

 


 

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