This time of year can really test us Spoonies out, can't it?!* I intended to write a blog about my own tips and tricks of how I get through the festive season with ME / CFS and electrosensitivity, but time has run out. I was also planning to launch my first Spoonie Warriors … [Read more...]
A Taster of My New Spoonie Membership Site – Coming in 2015
(I had this scheduled to post on December 22nd, 2014. I just saw it didn't got out! So here it is ... a little late for Christmas, but here it is anyway. Enjoy! And Happy 2015!!) If you read my blog regularly, you may remember me saying I'm working on a membership site for … [Read more...]
CFS / ME / FM Facebook Pages
It's sometimes so hard to find all the social media pages & people supporting others with CFS / ME / FM, so I've compiled a list of all the Facebook pages I could find, with summaries copied straight from FB. This first post is of CFS / ME / FM Facebook pages, and the next … [Read more...]
Day 25: 31 Days To A Better CFS Life – Letter To The General Public Pt 2 – How You Can Support Someone Who Has CFS / ME / FM
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...]
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