Australian ME/CFS Biobank

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The Australian ME/CFS Biobank is a partnership between patient charity Emerge Australia, researchers at La Trobe University, the Australian Red Cross Blood Service, Solve ME/CFS Initiative and the UK ME/CFS biobank.[1]

Funding[edit | edit source]

Funding of A$1 million was announced in August 2019, and an email news list was setup.[1]

The Mason Foundation, an Australian ME/CFS charity is funding the biobank.[2]

Partnership roles[edit | edit source]

Australian ME/CFS biobank awarded to research team which includes Emerge Australia!

The biobank and patient registry will be led by Emerge Australia, partnering with the Australian Red Cross Blood Service, Solve ME/CFS Initiative (SMCI) in the US, and the UK ME Biobank (UKMEB), making this a global project. This innovative project will make use of existing Australian Red Cross Blood Service resources, and will also benefit from the infrastructure of the UKMEB and resources being developed by SMCI. The biobank will store blood samples of ME/CFS patients, and matched healthy people, making these samples very useful for researchers.



News articles[edit | edit source]

Learn more[edit | edit source]

See also[edit | edit source]

References[edit | edit source]

Myalgic encephalomyelitis or chronic fatigue syndrome, often used when both illnesses are considered the same.

Myalgic encephalomyelitis or M.E. has different diagnostic criteria to chronic fatigue syndrome; neurological symptoms are required but fatigue is an optional symptom.<ref name="ICP2011primer">{{Citation

The information provided at this site is not intended to diagnose or treat any illness.

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.