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Thanks for your response. Like I said in my report, you can’t test for CNS over arousal you can only go off the symptoms you tell the doctors. They have worked with the illness now for a very long time. I can’t remember off the top of my head but I think it’s for a least 20 years or so...

Thanks to you and all others for your well wishes xx

Gladly My symptoms were Severe fatigue and exhaustion Little energy Post malaise Brain fog Slip of the tongue Poor sleep Severe pain and discomfort, mainly in my head Noise sensativity Chemical sensitivity Generally felling like really really lousy Palpataions Head rushes Tinnitus...

Thank you so much for your well wishes xx

Several people have asked me for this response so I’m hoping that it gets about to everyone. Firstly I would like to say this ward isn’t solely for people with M.E They also deal with Neurological disorders and illnesses that haven’t been diagnosed. They are just ill with an unknown reason...

Thanks for letting me know, I’ll get in touch with them.

I have had severe ME for 14 years now. Although since the start of the year I have come on leaps and bounds and finally starting to get my life back. This is due solely to an eight month stay in Leeds General Infmary on ward NICPM. This ward has been heavily criticised on forums on this...