Emerge Australia given $370,000 government grant


by Sasha Nimmo

Emerge Australia has been given $370,000 by the federal government in a grant for a research symposium, health and well-being surveys and to support people with Myalgic Encephalomyelitis and chronic fatigue syndrome.

“We’re really focusing on developing and delivering a lot of high quality support services as a result of this funding. We really do take our responsibilities as a national body seriously and we are aware that we hold a very particular space in the Australian ME/CFS landscape,” said Dr Heidi Nicholl, CEO of Emerge Australia.

Emerge Australia has more than 800 members around Australia. Around half of those identify as having chronic fatigue syndrome and the other half a mixture of ME, ME/CFS and other conditions.

Dr Heidi Nicholl joined Emerge earlier this year, taking over from Emerge’s committee of management member John Jeffries who stepped into the position of CEO for 12 months.

“The funding was given as a one-off grant for one year only. We are hoping that we can show how effective the funding has been and that we are a deserving cause for sustained funding,” said Dr Nicholl.

Dr Nicholl also asked the federal government for $750,000 for medical research.

Telephone support
Previously Emerge struggled to keep up with requests for help and could not return all phone calls coming in.

“There is money to support our info service – this will keep the phone lines running and enable us to answers questions and queries from Australians with ME/CFS and their carers,” said Dr Nicholl.

“We will be speaking to patients to make sure that we really do deliver what patients feel is needed and useful for them.”

Health and Wellbeing Survey
“We have funding to do an extensive survey into the health and wellbeing experiences of people with the condition. This will build on an initial survey that we did when we gathered data in 2015.

“We had run out of funding to complete the project but we’re now able to analyse and publish the initial data and we’ll be building on this with a survey in late 2018 / 2019.”

The initial Health and Wellbeing survey by the Federation University was begun nearly five years ago.

This project will receive $60,000.

“We’re also planning to be quite open about developing the next health and wellbeing survey so that patients feel like we’re asking the right questions about what is important to them,” said Dr Nicholl.

Support services
“Another part of the funding is to help us to consolidate and ‘future-proof’ our support services. We have various ideas for this and we’re forming patient advisory groups to help us to identify what should be prioritised”, said Dr Nicholl.

“We are one of a very small number of organisations working with people with this condition to help them to access the support that they need.”

Dr Nicholl outlined some of the ideas:

  • develop a handbook of treatments that can be tried – with notes as to the evidence base and likelihood of efficacy;
  • develop an Australian-focused online forum which would benefit people who can’t get to in-person support groups but who don’t want to (or can’t use) Facebook;
  • focus on patient stories to assist our advocacy messages.

International Research Symposium
Emerge have been given $150,000 to hold a research symposium next year.

“We have already appointed, and had the first meeting with, our science advisory board and we’re looking forward to holding a really great conference,” said Dr Nicholl.

“Emerge Australia is really beginning to consolidate its position as a leading voice in support and advocacy for people with ME/CFS. We now have a team of seven paid staff – all part-time – but we’re really developing as an organisation.”

Emerge has not yet announced the staff who’ve been appointed to the new positions.

See Emerge’s video of the announcement. Read more about Emerge Australia.

4 thoughts on “Emerge Australia given $370,000 government grant

  1. I would like to see some funding for educating doctors. As someone who has had ME at the chronic stage for 30 years, (a mild form since age seven) l don’t think we are in a better situation now than when l first started seeking help and a diagnosis.
    Instead of patients being able to walk into any surgery and be accepted, we are reliant on a narrow field of doctors who have an interest or knowledge of the illness.

  2. you speak of” support services. Can you please be specific as to what is meamt by” support services. ” specifying how a sufferer benefits. ghank you for specific accurate i formation because without it anything else has no meaning.

    1. Hello Denise,
      Emerge’s CEO outlined three of her ideas for support services in the article, as well as the telephone support service. Emerge would be able to give you more details if you contact them. If you have ideas, perhaps it would be worth joining their patient advisory groups?
      Thanks for reading.

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