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...]
Something To Brighten Up Your Spoonie Lives for 2015
So is anyone else finding this end of the year, pre-Christmas period extra draining physically, mentally and, dare I say, spiritually (how ironic!!)? Well, I certainly know I am! I've always got numerous projects on the go at once (if only in my head!), and trying to keep all … [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...]
The CFS / ME / FM / Spoonie Warriors Guides To … A Planned eBook Series. I Need Your Help!!
I am currently in the process of getting my first eBook - 15 Minute Power Plays With Your Kids: How To Be A Better Parent In 15 Minutes A Day - ready to launch on Amazon Kindle. As I've been learning about the process of launching eBooks on Amazon, it's re-kindled (haha) an … [Read more...]
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