In Part 1 of my Letter To The General Public From Those With CFS / ME / FM, I addressed a lot of the issues that our loved ones, family, friends and acquaintances may like to know about our experience of living with these illnesses. Here, in Part 2, I give some practical tips … [Read more...]
Day 24: 31 Days To A Better CFS Life – Letter To The General Public From Those With CFS / ME / FM – Part 1
For people living with CFS / ME / FM, one of the most challenging aspects of the illness is trying to explain it to other people – and have them believe us! Due to its invisible nature, CFS / ME, Fibromyalgia and other Spoonie illnesses are usually not able to be seen in any … [Read more...]
Day 22: 31 Days To A Better CFS Life – A Letter To Partners Of People With CFS / ME
I have always wanted to write some blogs about the challenges faced by partners of people with CFS / ME. I believe it is a topic that often gets neglected, and is something I'd love to see a lot more resources on. As we all know, it is incredibly tough for us - the people … [Read more...]