Foggy has asked M.E. sufferers to write him a blog post on their own personal M.E story. This lovely lady called Cat met Foggy at his launch and has written this blog post for him. Please read how M.E has affected her life. Hello Foggy, I would say my M.E journey has been a slow …
Hi, Foggy is in Tuscany! He had his first plane flight of this World Tour yesterday and loved every minute…I’m sure his tail will have wagged throughout the journey….;) This blog post was inspired by a Sunday afternoon chat I had with my Mum about our thoughts and guilt about the possible causes of my …
My name is Rhia. I am 22 years old and was diagnosed with M.E. in November 2016. I’ve had a lot of my symptoms for a few years, but they really started to show in 2015. M.E is a variable illness. Sometimes I can be absolutely fine and other times I feel so rubbish that …
Hello! Sally is having another one of her ‘I’ve been awake since 2.30am so will get up and do Foggy admin’ mornings. I’m on a cruise ship heading for Iceland but have just spoken to Sally via face time (;). Here is a blog about how my best friend Patch is not helping one of …
*Foggy* Hello! I have asked my fabulous Followers if they could write a guest blog post for me about their own personal M.E story. This is the first of this campaign. Please read this blog post from Lynne, North Shields, Tyne and Wear, UK . Being diagnosed with an invisible illness has to be one …
Hello! Foggy is enjoying his well-earned break in Foggy HQ and while he is snoring I thought I’d write this blog to tell you how I have been health-wise to since the last campaign ended. My ‘vertigo’ lasted 3 and a half months before it was finally diagnosed as chronic migraines. Which is EXACTLY what …
Hi, Throughout Foggy’s life I have made a point of saying I am lucky enough to not suffer from M.E./C.F.S chronic pain. However, things have started to change over the past 3 months. I am currently undergoing tests and physio to try to deal with an extremely painful right arm. RSI, Carpal Tunnel and Tendonitis …
Hello, I have been pondering why M.E. doesn’t have celebrity advocates like other illnesses do. Every charity has ambassadors that do their utmost to raise the profile of the charity at every given opportunity. I remember when I was doing the last campaign I asked the ME Association if we had one, with the hope …
Hi, This blog will hopefully address the issue of M.E sufferers bearing children. Let me begin by saying that I consider myself to be exceptionally lucky; I have never had a maternal bone in my body and so having M.E is not a deciding factor in whether I have children or not. I have never …
Hi, I have woken up feeling very M.E’y. While I am feeling IT I am going to try my best to describe what IT feels like. In today’s case, IT is extreme fatigue and disequilibrium. The combination is definitely a bit of a mind blower in terms of adjectives! My entire body seems to have …
