M.E. is not for Wimps

There are way over 250,000 sufferers of M.E. in the UK with about 25% classified as being severely affected, i.e. bed/house-bound. Each sufferer is a member of a family affected by M.E. I have personal experience of living with M.E so I understand what devastating effect this illness can have on someones life, their family and friends.
I am raising funds and also raising awareness into ME with the medical professions, by leaving literature at my local doctors and hospital.
I was recently in hospital; Suffering severe chest pains and breathlessness. I came up against some doctors who had never heard of ME or CFS, the first night of my stay I was almost sent home, until I collapsed after being made to walk up the corridor. The next day until I explained my old job as an Advance Personal Trainer and Sports Therapist that was struck down with Viral Meningitis several times and then went onto develop ME, was I then given the respect I deserved. The consultant I went onto see and his team were marvellous and without their support I may not be here to tell this story, as he knew about ME and looked beyond my ME and treated my condition as an individual. I do not want this to happen to anyone else, we need to get together to dig deep ourselves. I would be very grateful if you are able to donate something and support me in making this centre real, making ME known as a disabling illness with treatment for us all.