Tag: funding

Australian advocacy

ME patients forgotten in government decision-making

Parliament was told that 75% of Australians with ME and CFS recover. The real figure is closer to 5%.
Why would the government allocate funding for medical research and treatment if it is told that most patients recover without it?

Australian advocacy

Write to your representatives, take action!

Need a kick-start to writing a letter? This is a letter template to help you write to politicians and bring attention to the issue of support for people with ME and CFS.