Story
Hi my name is Becky and I have M.E. (Myalgic Encephalopathy)
This year marks 10 years since I became ill with a winter bug and then later diagnosed with M.E.
M.E is a life changing condition with multiple symptoms including: Post-Exertional Malaise, Persistent Fatigue, Cognitive Issues, Pain, Dizziness plus many many more. There is no one specific treatment and no cure.
To mark 10yrs of living with this condition and thank ME Association for all they do, I am fundraising by live-streaming 10hrs of virtual truck driving, under my gaming name AngelRoar24, on YouTube during May.
Please help us to support people with ME and their families.
ME (Myalgic Encephalopathy), or Chronic Fatigue Syndrome, blights the lives of over 400,000 people in the UK today. The smallest exertion can floor them; their joints and muscles ache unbearably; restful sleep eludes them; and ‘brain fog’ clouds their thinking. It changes lives drastically – disrupting study; making work impossible; and straining family relations to breaking point. Many sufferers cannot leave their homes. There is no known cure.
Please help us to help them.
