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  1. About us
  2. Our team

Team

Check out the great people working behind the scenes at Emerge Australia.

Staff

The Emerge Australia staff members

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Anne Wilson – Chief Executive Officer 
Dr Richard Schloeffel OAM – Medical Director 
Simone Eyssens – Research Director
Amy Gibson – Operations Manager
Laura Allen – Health & Support Services Manager, Telehealth Nurse 
Jessica Kauhausen, PhD – Biobank Coordinator (Maternity leave)
Michelle Tavoletti, PhD - Research Manager 
Rochelle Lade, PhD – Education and Programs Manager
Kate Herbert – Nurse Educator 
Laura Kool – Operations Officer
Susan Sayer – Donor Relations Manager 
   John Jeffries – Ambassador

Published: 18th June, 2019

Updated: 13th April, 2022

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Volunteers

Our fantastic team of volunteers

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Jenny – Parliamentary Liaison Officer

Carol – Data Management

Maria – Information Line

Jason - Communications 

Jen - General support 

Louise, Jolien, Sarah – Research Digest

Jop – Storyteller

Gretchen, Dave - Online Forum

Published: 21st June, 2019

Updated: 8th November, 2021

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Board

The Emerge Australia Board

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Mark Clisby - President
Senior roles in the public sector, universities and NGOs, CEO of two social enterprises

Martin Wilkinson – Vice President
Director of Clinical Studies for a not-for-profit healthcare company

Andrew Bretherton – Secretary
A banking lawyer with over 40 years experience

Russell Smith – Treasurer
Accountant and passionate supporter of not-for-profit organisations

Rebecca Davey
CEO, Arthritis ACT

Caitlin Phillips-Peddlesden
International development expert, Oxfam Australia, specialising in monitoring and evaluation

Published: 8th November, 2019

Updated: 6th January, 2022

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Showing 10 of 3

Latest

  • Our GPs need to know what to do: We have the plan, we need the funds

    Our GPs need to know what to do: We have the plan, we need the funds

    Emerge Australia has written a 5 years plan for GP Education about ME/CFS, Long COVID and post-viral diseases, accessible to all of Australia’s GPs.

  • What will it take for Australia to get new clinical guidelines for ME/CFS?

    What will it take for Australia to get new clinical guidelines for ME/CFS?

    $1,200,000 is required over 2 years for the development of national clinical guidelines for ME/CFS It is a matter of urgency for Australia to update its clinical guidelines for ME/CFS, to ensure Australian ME/CFS patients have access to the best possible care, based on current understanding of the condition and latest evidence.

  • Australians with ME/CFS need Optimal Care Pathways

    Australians with ME/CFS need Optimal Care Pathways

    $1,100,000 is required over 5 years for an Optimal Care Pathway for ME/CFS. Optimal Care Pathways (OCP) support integrated shared care across the entire health system. Such innovative approaches to the coordination of non-clinical service delivery have achieved improved outcomes for patients in other settings.

  • Changes to the Support and Services programs

    Changes to the Support and Services programs

    With the completion of our Patient Pathways telehealth pilot program on June 30, 2022 we will be making some changes to how the service works and the programs it delivers.

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  • What is ME/CFS?

    What is ME/CFS?

    Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex and disabling disease that affects many parts of the body, including the brain and muscles, as well as the digestive, immune and cardiac systems, among others.

  • Contact Us

    Contact Us

    Emerge Australia provides an information line where you can find out about the latest news and information about ME/CFS.

  • What we do

    What we do

    Who we are and what we do

  • Volunteer with us

    Volunteer with us

    Join our small, friendly and enthusiastic team as a volunteer

  • How is functional impairment assessed?

  • Coronavirus and ME - Simplified facts

    Coronavirus and ME - Simplified facts

    Many people with ME/CFS and other vulnerable communities in Australia are concerned about the impacts of the spreading coronavirus disease COVID-19. This is an easy-read resource with the latest information and advice.

  • Annual reports

    Annual reports for Emerge Australia

  • Symposium

    Replace this with your content

  • Patient Advisory Group

    Patient Advisory Group

    The Patient Advisory Group provides Emerge Australia with ongoing advice about the needs of the community, as well as invaluable input into projects

  • What is ME/CFS?

    What is ME/CFS?

    Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex and disabling disease that affects many parts of the body, including the brain and muscles, digestive, immune and cardiac systems. ME is classified as a neurological disorder by the World Health Organization.

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Get in touch with us

Emerge Australia
Level 7, 276 Flinders Street
Melbourne VIC 3000
1800 865 321
03 9529 1344
Media enquiries: 0400 165 391
 

Emerge Australia is registered as a charity with the Australian Charities and Not-for-profits Commission (ACNC). We are authorised by the Australian Tax Office as a deductible gift recipient (DGR). 

ABN/DGR: 22 385 438 041

Donations of $2 or more are tax-deductible. 

Emerge Australia acknowledges Aboriginal and Torres Strait Islander people as the Traditional Custodians of the land and pays respect to their Elders past and present.

© 2019 Emerge Australia. All rights reserved.