Article Update 7th June 2010 I have found the information from a friend of mine who was diagnosed with CFS/ME and then with Lyme Disease. Here it is: http://www.prohealth.com/fibromyalgia/library/showArticle.cfm?libid=13020&B1=EM061709F This is what she has to say about the protocol: Marianne, Saw this article this morning and thought it was just about the best article about […]
Having been in receipt of quite a few emails about CFS/ME Organisations and Petitions I thought: ‘I don’t want to know.’ ‘I am not interested.’ I am so fed up of hearing about how the Government are not listening and not caring about those with CFS/ME. I think to myself, what about all the other […]
There seems to be a drive like never before about Natural Health. Reference: Dr Whitaker Health Freedom It is as if we don’t know that Natural is Best. I think Every One would say they eat naturally and know what is good for them but do indulge in the sweet sticky foods every so often. […]
Many moons ago, in the deepest darkest part of my CFS/ME journey I was introduced to a fish oil called PuraEPA, which is a denatured fish oil with the essential brain and heart nutrient, DHA, taken out. The theory by Professor Pura is that CFS/ME people couldn’t make the conversion in the body to use […]
As I said to one reader of my website – don’t call it a relapse, call it a smack on the wrists for thinking you could do so much.
April 2009 I thought I would put this as a link rather than an entry to the Diary I have written on my experiences with the Perrin Technique. I was trying to explain to a relative I had not seen for some time on how I used to feel compared to how I feel now. […]
Read this advice before attempting the stretch routine.