As you may know by now I am having a charity tea party in ‘celebration’ of M.E. Awareness week. My closest friends and family are coming over for an afternoon of tea and cake on Sunday 11th May, now dubbed Blue Sunday. (The awareness colour for ME/CFS is blue.) As I have made so manyContinue reading “The Final Countdown”
Category Archives: #Chronicillness #invisibleillness #mecfs #cfs #NeuroME
Outfit of the Day spoonie-style
There are so many bloggers out there who now make their living by telling people what it is that they’re wearing. I won’t lie, I don’t quite get it. I mean good on them for seizing the opportunity but, personally, I’m more than capable of choosing clothes from my wardrobe without needing to search for inspirationContinue reading “Outfit of the Day spoonie-style”
Stigma
NB. If I was reading this out loud I might get a bit ‘shouty’. I am developing quite a large chip on my shoulder and it is all your fault. Well society’s fault really but let’s not waste time splitting hairs. If I didn’t have the ‘M.E. label’ medical professionals would surely be atContinue reading “Stigma”
M.E. myself and I 