Hello!! Foggy is currently having a wonderful time with the Neighbours on Ramsay Street in Australia and so has allowed Sally to write this blog post. There is big news in the world of M.E. and he thinks Sally should highlight it. So here goes… Hello, Last night the Institute of Medicine in the US …
Hi,I deliberately keep this campaign light and upbeat as I feel there are more than enough heart wrenching ME life experience blogs/campaigns/websites in the world already. I am trying to make this campaign engaging and enjoyable to follow whilst highlighting the awfulness of this increasingly common debilitating illness. I think non sufferers do not understand …
Hey! Foggy thinks Sally has been pushing herself a little bit too hard and wishes she would/could slow down a bit (Not possible Fogs). Foggy would like his non-M.E. sufferer Followers to understand why work demands can make symptoms worse. He is going to use Sally’s typical work day as an example to show how …
Hello!Today Foggy wants to talk about Pacing therapy.When Sally was first diagnosed (it took them 3 years to work out what was wrong!), she was told to ‘pace’ herself and to think of her energy levels as a battery. She should always try and keep her energy battery half full. ME sufferers never have a …
I want to remind you of the reason I have created this fun, upbeat, globetrotting campaign. M.E. is a massively misunderstood, under-researched, increasingly common debilitating illness. I’m ‘lucky’ in that I ‘only’ have mild M.E. Fortunately, this means I am still able to work full time though with difficulty some days. My symptoms are: Extreme …
