For people with ME, energy must be carefully rationed and I am incredibly grateful to those who chose to spend some of this energy sharing their experiences with me by participating in my PhD research. I will continue to advocate for your stories to be heard.
#SevereME #SevereMEMonth #MEAwareness
Advocacy must continue to ensure that the debilitating and widespread impacts of ME are recognised in Australian healthcare policies. Importantly, vital services must be readily accessible for people with severe ME who are too unwell to present to healthcare centres.
#SevereME #SevereMEMonth #pwME
The profound, disabling impacts of living with ME are often invisible, both due to the illness’ symptoms and isolating nature. This is magnified for those living with severe forms of ME who are house- or bed-bound.
#SevereME #SevereMECFS #SevereMEMonth #MECFS #MECFSAwareness #MEMedia #MEAction
Although Severe Myalgic Encephalomyelitis (ME) Awareness Month is coming to a close, people living with this complex chronic illness will continue to be impacted by its challenges and burdens.
#SevereME #SevereMECFS #SevereMEMonth #MECFS #MyalgicEncephalomyelitis #pwMECFS #pwME #MEAwareness
