If you are frustrated by the condition of CFS/ME because you suffer from it or because you are a carer or know of someone with it then read the following article from the Manchester Evening News. It is very encouraging and I wonder if we are now at last within a hair’s breath of an answer and treatment to CFS/ME!
Click on: Unlocking the secrets of ME
Please see: Osteopathy & Chronic Fatigue/ME
I am constructing an A-Z spreadsheet of treatments for CFS/ME that will contain the following information: Name of treatment Type – physical – mental Success rate (anecdotal or objective) Cost of treatment: Ranges from £30 to £95 to £120 Number of treatments before a reduction in symptoms: Not known/20 Website – Yes/No please see: Clinical […]
At last a treatment for CFS/ME that makes perfect sense to me. It says what it is, and what can be expected, it is down to earth and obvious. As the character Henry Higgins, played by Rex Harrison in My Fair Lady, said: ‘by jove I think she’s (they’ve) got it!’
But that is the age old question – which came first, the chicken or the egg?
5. Do you think that your patients have a right to know every aspect, experience and qualification that you and your practitioners use on your patients? Can you list those aspects here?
A diary of CFS/ME feelings written since November 2005. The present date is first with the first date last!
‘Approximately 181,827 people in the UK are suffering silently behind closed doors and no-one knows why. Some GPs even now tell patients with this illness that they are malingerers. There are no real treatments or medications to help or cure the symptoms. The symptoms can be so severe you feel like you are dying. Why isn’t the government doing more to understand and help those suffering?