The Australian Parliament is asking for public submissions into chronic disease prevention and management in primary health care. This is our opportunity to write to them and ask them to fund research into Fibromyalgia and cater for patients who require home care, visits and support from medical professionals.
Despite an estimated one million Australians living with Fibromyalgia, there is limited services, support and information available. The gaps between research and daily care are unacceptable.
Now is the time to ask the Federal Government to provide:
- Leadership and coordination of a national approach to provide integrated management of Fibromyalgia services, building on the work of state governments, private sector providers, Medicare Locals and Local Hospital Networks.
- Access to quality services for all Fibromyalgia sufferers including people in rural, regional and remote areas, indigenous and socio-economically disadvantaged communities, children, and older Australians.
- Access to education and training for health professionals in particular as it relates to early intervention, multidisciplinary team practice and the early identification of Fibromyalgia.
- A public awareness campaign to address discrimination, misunderstanding and stigmatisation of people with pain within the community, including in the workplace and in welfare and compensation systems.
- Funding to provide community support services including consumer information, self-management education and telephone support (crisis help line).
- The development of a national research agenda to address gaps in knowledge about Fibromyalgia and improve clinical practice in pain management.
The deadline for submissions is Friday, 31 July 2015.
Please make a submission if you can.