It’s been a long time since I properly updated this blog and so many things have happened, I haven’t known where to start. There’s a lot I have no idea how to begin to explain. I’ve learned so much over the past few years and although there have been many times I’ve despaired or wanted … Continue reading An update…
Tag: me/cfs
I see bravery everywhere…
Some days it scales mountains, other days it takes one step outsideI’m sure bravery raws some days. And others it whispers, “I’m not ok”Sometimes it sounds like, “I was wrong” or “I’m sorry”, “I see your point of view”Some days bravery paints a daring masterpiece. Others it dares to make a single brush strokeYesterday it … Continue reading I see bravery everywhere…
ME/CFS Awareness Week- what can you do?
(Reposted from Instagram) I got ill around 4 years ago, though I had symptoms for 10+ years before that. The pandemic has shown everyone how hard it is to have our freedom taken away, yet this is an illness with so little awareness and research, you can feel invisible. There are so many who experience … Continue reading ME/CFS Awareness Week- what can you do?
A view of the pandemic from 2.5 years housebound
Before I begin, a little update on my health, as nearly a year has passed since my last post… 2019 was a bit of blur to me as I spent most of it very unwell, unable to go out, so that days, weeks and months merged. My health deteriorated further mid-year, after eating something bad, … Continue reading A view of the pandemic from 2.5 years housebound