(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?
Tag: cfs
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
