Chronic fatigue caused by brain injury due to glandular fever: study
|
|
|
| Posted
:
Thu, 02 Mar 2006 18:02:00 GMT |
| Author
:
Emma Price |
| Category
:
Health |
| News
Alerts by Email ( click
here ) |
|
|
|
Health News |
Home
|
|
|
Those suffering from chronic fatigue syndrome might be experiencing temporary brain damage caused by glandular fever, a study, by University of New South Wales, has found. Glandular fever, which is caused by Epstein-Barr virus, is characterized by fever, sore throat and fatigue, whereas chronic fatigue has symptoms like muscular weakness, pain, cognitive and digestive disturbances, hypersensitivity, depression and most importantly, low stamina and energy.
Likening the action of the Epstein-Barr virus on the brain to a hit and run accident, Andrew Lloyd, lead author of the study, said, It's an injury in the sense that it wasn't there people were perfectly well something in the acute phase of the illness went wrong and then it slowly recovers like a broken arm or a broken leg. It's just that in this case its taking weeks to months rather than days or quicker.
Under the study, the researchers, led by Lloyd, tracked the long-term health of subjects who had contracted the Epstein-Barr virus (EBV), Ross River virus (RRV) or Q fever. Around 39 subjects were afflicted with acute glandular fever, of which eight developed a 'post-infective fatigue syndrome' that lingered for over six months. Thirty-one of the subjects recovered without any fatigue. The researchers also studied the activity of the EBV in the blood of the eight over a period of one year.
Our findings reveal that neither the virus nor an abnormal immune response explain the post-infective fatigue syndrome. We now suspect it's more like a hit and run injury to the brain. We believe that the parts of the brain that control perception of fatigue and pain get damaged during the acute infection phase of glandular fever. If you're still sick several weeks after infection, it seems that the symptoms aren't being driven by the activity of the virus in body, it's happening in the brain, Lloyd said while explaining the findings.
Chronic fatigue syndrome has baffled researchers and doctors worldwide, ever since it was recognized by the World Health Organization in 1969. However, a number of doctors have refused its diagnosis, leading to a stigma being attached with the mysterious disease. But lately, attitudes seem to be changing towards the disease, with many doctors and medical authorities emphasizing on the need to accept that the disease exists.
I personally have never had a doubt that it's real because there are people who have got a set of symptoms that are unexplained. The real versus not real thing is often caught up in the mistaken notion about malingering or it's all depression but really there's no evidence to support that. So in a nutshell yes, it (the study) clearly supports the argument that it's real, Lloyd said.
He added that the symptoms show that the problem is related to the brain rather than being physical. It's not too big a leap of faith to say after that, it's in the brain, because of the nature of the symptoms it's fatigue, it's pain, sleep disturbance, concentration and memory difficulties and mood disturbance. They're very much brain symptoms, Lloyd said.
The findings of the study have been published in Journal of Infectious Diseases.
Copyright,
respective author or news agency
|
|
|
|
|
|
| |
|
Help!
By:
Jill Warren ,
Mon, 03 Jul 2006 11:37:56 GMT |
|
I would like to talk to you Gina - I have Skype set up on my computer - how do I find your site? I am sick of nobody understanding what it is like. I think you helped a friend of mine a few years when I was at University. If you could help me that would be great!
|
|
glandular fever help services
By:
Gina Burton ,
Mon, 03 Jul 2006 10:54:10 GMT |
|
I have been helping people with chronic glandular fever (infectious mononucleosis) problems for 9 years now, via my web site.
I am not surprised, but still very interested in these findings re glandular fever and the brain. For anyone who has continued to suffer bad bouts of health and very low energy after glandular fever, they would know that during the bad days, it is as if you suffer a change in personality and certainly something in the brain would appear to be distorted! I am sure our families and friends would agree with me on this point!
If anyone is interested in looking for some practical help, advice and guidance then please look at my site.
As part of my service I include a free assessment consultation via Skype or regular phone. I am willing to speak to anyone who is interested in trying to do all they can to really try and entice thier body back to a more "normal" existence.
|
|
Glandular fever
By:
Hayley ,
Thu, 18 May 2006 11:36:40 GMT |
|
I had glandular fever about 17 years ago and was extremley ill for months, i saw several doctors who did not diagnoise it and suggested it was all in my head, i was eventually diagnose via a blood test, i still suffer with the side effects, i catch any virus going around and have periods were i haven't even got the energy to talk, this is extremly difficult especially when working and time off sick, i did see a doctor many years later who explained to me that glandular fever suffers will get any virus/cold going and it will take 3 times longer to recover, when i get an attack the only thing to do is rest in bed.
|
|
julie
By:
Seb ,
Mon, 27 Mar 2006 11:46:04 GMT |
|
Any way of getting in touch with Julie? Her daughter seems to be experiencing similar symptoms to me, and I'm eager to find out more...
|
|
recent
By:
Seb ,
Mon, 27 Mar 2006 11:26:18 GMT |
|
i had glandular fever nearly a year ago. It had gone but now I have a regular malaise - neck aches, head pain and feeling of tiredness and woolyness. Is this CFS? It tends arrive following a cold or when I'm worn out. Has anybody any remedies that has worked for them? thanks.
|
|
CFS
By:
RAF ,
Tue, 21 Mar 2006 16:39:03 GMT |
|
my wife had glandular ferver at here 15th.
eversince here parents and hereself complains thath she hase never was the same.
now she suffers from cfs, and the insurance companies are using the psycicale therms for not paing the care (belgium
|
|
thank you!
By:
Julie ,
Wed, 08 Mar 2006 01:33:24 GMT |
|
My 21 year old daughter has been suffering with symptoms of what I have called 'glandular fever relapse' for over 3 years. Doctors will not listen to this and look for other things like depression and low iron levels. It has been a very frustrating time so it is wonderful to finally have an answer, a reason. Not that it makes it go away! I would like to know if there is more long term research being conducted investigating methods of recovery.
|
|
Brain Attack
By:
Claire ,
Sat, 04 Mar 2006 00:59:51 GMT |
|
I had Glandular Fever in 2000 & have suffered with Chronic Fatigue eversince. Two large turning points for me has been taking "MACA" which is a herb derived from the Maca Root that enhances brain function & stabalizes hormones. Before MACA, I would frequently forget things such as my boyfriend or best friend's names or even which side of the road to drive on. MACA has helped me maintain brain clarity. Also an 18 month Homeopathy treatment has brought me within the reaches of functioning & participating in the real world. I'm not completly free of the syndrome but now at least I know in which direction to focus my endevours to conquer it.
|
|
news
By:
emma ,
Fri, 03 Mar 2006 12:52:01 GMT |
|
I had glandular fever when I was 14, it was only discovered after six months of returning home from school and falling asleep constantly. I am 24 now and since I was 14 I have found it very difficult to function in everyday society. I dropped out of school because of all the symptoms described in CFS. I have never been diagnosed and thought that it was something wrong with me that I was just 'lazy'. I have fought it every step of the way though, and now currenty nearly at the end of my degree, but it has been so hard and I have suffered from depression. Reading this has helped me so much see what was really happening to me over the years, a kind of relief that there is not just me going through this.
|
|
Nice work
By:
Brad funnell ,
Fri, 03 Mar 2006 04:34:40 GMT |
|
I have had CFS now for neily 7 years.Maybe because i have had [EBV] twice, and ross river,and [CMV].It has not been a pleasent time for me to say the least.
But news of this new reaserch does bring some light to the subject,especially now celebrties= Ian thorpe etc is bringing it to the head lines. I dont Know what to say, i just feel, i suppose, for those who are worse off than me. My condition has some what improved buy unable to hold down a job due to the unrealiablty of the iIlness.
Life goes on.Anyways thanks for listning...
Brad
|
|
news
By:
jessie ,
Thu, 02 Mar 2006 18:38:23 GMT |
|
very informative
|
|
|
|
|