Stop fiddling while Rome burns guys. Turn your attention to actually finding a cure for this disease. And if you want a new name, simply call it Living Hell Disease.
Severe ME/CFS Information Pack
Severe ME/CFS is a cruel and physically disabling illness which wrecks the lives of thousands in the UK and millions worldwide. I know because it took my life for several years. One of my promises back then was to do all I could, when able, to help the Family and Friends of Severe ME/CFS Patients understand the nightmare that their loved ones are going through; what Patients and their Carers have to battle against every day, and how the understanding, support and compassion of Family and Friends can make such a dramatic difference to their speed of recovery. Hence this Blog and My Severe ME/CFS Information Pack now available as an e-book. I do so hope that both help guide you through the hellish maze that is Severe ME/CFS
Email email@example.com for details
Severe ME/CFS...Time for a cure not a new name
Stop wasting money on a new name...you could have spent the US$1 million this report cost to conduct research into actually helping Severe ME patients. As if Chronic Fatigue Syndrome wasn't bad enough...now they've come up with a new moniker: systemic exertion intolerance disease (SEID). I can hear the cruel jokes already...
Posted by Blogger Catherine