Life With M.E
![Image](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhfNJzVRPNbV3tYoObRCt-xhgTY12AltWR2Qn7fbdb69KW-hTTdREJByYegwkqmeslSTopoPaIWqjlnamedaH5lnP3XHOQrXM_cOCntHBdZ5fYsgE7sYFciHFD7pBUn0crYFDH08sDkZ2Eh2ZDWsl3Nq1lJawkeOrWuPmtzKOSWtg3sccNCMgOk4pNMsA/s320/CjdA_zIWYAA_ZIo.jpg)
May is M.E awareness month, after 33 yrs of living with it & campaigning I kinda hoped we'd be somewhere by now where awareness wasn't needed, and I wouldn't be here again boring the pants off you, but unfortunately that's not the case, there's still alot of ignorance surrounding M.E (No we're not a little tired) and there's still no treatment and no cure, so here I am once again to hopefully give those of you unfamiliar with the illness a very brief insight that I hope will help, next time you hear it mentioned. M.E known by it's medical name Myalgicencephalomyelitis (Yes I know, let's just stick to M.E) is still classified by the World health Organisation as a neurological disorder, It's often referred to as a "lingering death" because quite frankly that's exactly how it feels. The illness is a complex chronic one that affects the whole system, physical and also sensory, from a whole body exhaustion, to cardia