Myalgic Encephalomyelitis and Chronic Fatigue Syndrome research are ongoing.
For more recent CFS/ME research results move here.
This article shares research that procedes 2012. Of course most of this research is timeless - It lets us know the science behind the illness and raises our hopes of better diagnosis and treatment in the future.
Please note, this article may be biased towards the results of ME and Chronic Fatigue Syndrome research in the UK, since I subscribe to magazines that are written in the UK.
Contents for Chronic Fatigue Syndrome Research- click on a link when there is one, or please scroll down2012
ME / Chronic Fatigue Syndrome Research at 10 Dec 2012
A key difficulty experienced by ME/CFS patients is standing, most especially standing still. Symptoms ensue, such as dizziness, altered vision, nausea, fatigue, etc.
(Sounds familiar to me.)
It is speculated that if a test for orthostatic intolerance can be established it could be used as a diagnostic marker for those with ME/ CFS.
Click through to read more about ME research into orthostatic intolerance.
Blog on Multiple Sclerosis, 24 August 2012
Some visitors to this website have Multiple Scelerosis. The blog below is also relevant to this page of Chronic Fatigue Syndrome research since it deals with research into an auto immune disorder.
Rosary Solimanto links through to MS research on how "beta-amyloid may be able to combat MS by damping down the autoimmune reactions that are the disease's hallmark". Excellent news.
ME/ Chronic Fatigue Syndrome research, July 2012
Iron pills reduce tiredness in a random controlled study of 198 French women suffering with fatigue. Note that they already tested with low or borderline iron levels.
You can increase your iron levels by eating a lot of green leafy vegetables.
The supplement Floradix has been recommended to me on a number of occasions, although personally I experienced no marked improvement when taking it.
Please note that this research was not into those with CFS but only those with chronic fatigue.
ME / Chronic Fatigue Syndrome research, July 2012
I have just listened to an interview with author, Katina Makris who talks about having an undiagnosed illness for five years only to end up finding out that she had Lyme Disease.
If you have ever been bitten by a deer tick, this will be of interest. I was bitten by a tick more than once.
I was fascinated as Katina talked about the three distinct stages of Lyme Disease.
1. Immediately after the tick bite there can be flu like symptoms of aching and tiredness. If you are lucky you are alerted by a rash, but only 50% get this. Untreated, the person can then seem to recover.
2. Some months later symptoms such as severe migraine and digestive upset. It may also affect the nervous symptom with anxiety starting.
3. The person is diagnosed with a neurological illness such as MS, Parkinsons or dementia.
You can find out about the alternative healing therapy which helped Katina in her book Out of the Woods.
I recommend this book. It is a very well written account of what it is like to suddenly find yourself living with serious illness, without a diagnosis, and how that impacts on your life and relationships.
Click to read about other chronic illnesses which need to be excluded to avoid a misdiagnosis of Chronic Fatigue Syndrome.
Myalgic Encephalomyelitis / Chronic Fatigue Syndrome research, April 2012
Voices from the Shadows is a deeply moving and compelling film which
witnesses to the hidden lives: the 'voices from the shadows' of those
suffering from ME, especailly children and younger adults.
DVDs of Voices from the Shadows are available to order online.
Cost £6 plus p&p.
A useful film to help understand or communicate the severity of CFS/ME.
UK research in one area of the UK shows that CFS in children is more common than previously believed. The chronic illness could affect as many as 1 in 100.
Myalgic Encephalomyelitis / Chronic Fatigue Syndrome research, November 2010
As from November 2010 , those with ME/ CFS have not been allowed to donate blood in the UK.
To read more, type into a search engine "Can someone with myalgic encephalomyelitis donate blood". (I had linked to an article before but they removed the page.)
A number of other countries followed the UK lead and banned blood donations from people with ME/CFS. These countries include Australia, Canada and New Zealand.
NHS Blood and Transplant explained the ban as being "a precaution to protect the donor's safety by ensuring their condition is not made worse by donating blood".
Visit the wonderful CFS blogs of those below with whom I have been in contact. There are a lot of beautiful people out there, living with chronic illness with great courage...
The Light shines brightly when it shines in the darkness.
Click through for a separate page of articles on research into CFS and exercise:
Move to the home page: Healing Chronic Fatigue Syndrome.