It's been a while hey? So where have I been in the last few months? Well, for 3 weeks of it I was living the dream in the USA. And when I say "DREAM", I mean that in my wildest dreams I truly never thought I'd get to do something like that again. But I did!! :) My Big US … [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...]
Needs Must … Sometimes We Just Have To Live A Little
(I started this blog 2 weeks ago, but you know how it goes ... my recent health challenges have meant I haven't finished it until now. Part of the reason was also that I wanted to do the blog justice & include lots of photos to really give you a feel for why THIS event was so … [Read more...]
Cheers to the Earth Angels in Our CFS Lives
Isn't it lovely when someone unexpectedly helps you out? Today my Mum was in town and spent the morning cleaning and tidying my house that had got out of hand while I've been wrestling my little stomach parasites to the ground and evicting them from my body (see previous post … [Read more...]