What is it like to live with ME/CFS? How hard was it to get an accurate diagnosis? When did it start and how has it affected your life? What tips can you offer to others who may be looking for help / hope? These are the kind of stories we are looking to gather to share with other readers.

Reading a person’s real-life experiences can be incredibly helpful for others who are dealing with the same health condition. Sure, there are the predictable trials and tribulations that come with having a chronic health issue, but hopefully there are also some valuable treatment successes as well. And perhaps just as importantly, it’s a way of knowing that none of us are ever alone.

Please contact abbey@me-cfs.org.au [1]