12 May Awareness Day

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Panel of international medical experts publish in-depth ME/CFS guide for children and adolescents

Give a Little Love Foundation is putting the FUN in fundraising

Blood, Tissue and Organ Donation with ME/CFS

Have you asked yourself the question: can I donate blood, tissues and/or organs even though I have ME/CFS? Well, the simple answers are no, and maybe. See below: Blood The Australian […]

Do Something for ME

Do you have an idea for raising awareness and/or funds to spread the word about ME/CFS?  Being a Community Activist and raising awareness about ME/CFS is a lot simpler than […]

12 May Awareness Day

Each year on 12 May people all around the world hold events to raise awareness and honour those with ME/CFS and related conditions such as Fibromyalgia and Multiple Chemical Sensitivities. […]

Post Exertional Malaise (PEM) and Graded Exercise Therapy (GET) in Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) by Simone Eyssens

We are really pleased to endorse this comprehensive primer (review) article by Simone Eyssens which presents the latest research evidence and highlights the potential harm from Graded Exercise Therapy for […]

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Panel of international medical experts publish in-depth ME/CFS guide for children and adolescents

A panel of international medical experts including doctors from Australia and New Zealand have written and published an  in-depth Diagnosis and Management in Young People primer, open-access for viewing here. […]

Give a Little Love Foundation is putting the FUN in fundraising

Give a Little Love Foundation invites you to attend the next fundraising Comedy Night in support for our organisation. The target of $50,000 will be used to help us grow […]

ME/CFS patients are demanding Justice

ME/CFS patients are demanding Justice Uk author Nathalie Wright developed the article ‘Time for Unrest: Why patients with ME are demanding justice’, which reports on the struggles patients face to […]

Scientists may finally be finding their footing

According to Maxmen (2018), she states that “Despite the setbacks and the long delays, many argue that science is operating as it should- being self-critical and open to revision. In […]

me/cfs

Turning with hope to 2018

Turning with hope to 2018 A message from the CEO As we approach Christmas and the end of the year, we turn with hope for 2018. Reflecting on 2017, there […]

Global progress of ME/CFS 2017

Global progress In January… o Queensland Scientists at Griffith University found strong evidence for a defective cell receptor appearing to be central to the development of ME/CFS. The researchers “confirmed […]

Moving film, Unrest “opens your eyes” – Emerge’s President

Moving film, Unrest “opens your eyes” – Emerge’s President Emerge Australia’s President, Sally Missing, attended the Gold Coast screening of the documentary “Unrest”. Sally said, “The film was not diminished […]

NHMRC Expert Advisory Committee welcomes Simone Eyssens as consumer representative

Emerge Australia was invited to nominate a consumer representative to the NHMRC Expert Advisory Committee. We are delighted that our nomination Simone Eyssens, who many of you will know through […]