Hey guys I’m feeling pretty beaten down and frustrated, I live in Australia and work full time and deal with pain, fatigue and light sensitivity all the time. I’ve been researching help I can get from the government to support me in any way in terms of the cost of treatments etc and I’m not finding anything except the National Pain Strategy which is all about teaching people about treating chronic pain with no support for people with chronic pain. Basically I want to know if any other Australians with MS have been able to access the NDIS or any other support services for their pain and illness? Is it work getting heath insurance? And if so what insurance are you with that covers your pain management the best?