Chronic Fatigue Syndrome, Environmental Illness, and Low White Blood Cell Count
Posted by: Maff
on May 12, 2010
I feel I must apologise for my recent lack of blogging activity but I'm sure when I explain why you'll understand - plus the reason has given me the inspiration for this post!
As regulars will be aware I have suffered from Chronic Fatigue Syndrome (ME/CFS) for a long time - since I was 11, so 20 years now. Like many ME/CFS sufferers I am also burdened by adrenal fatigue, low thyroid function, hypoglycaemia, Candida and Small Intestinal Bacterial Overgrowth (SIBO) amongst other things. I also suffered from severe Multiple Chemical Sensitivity for a number of years in my early 20s but thankfully was able overcome it (touch wood)!
Like most suffering from environmental illnesses (or more appropriately here 'invisible illnesses') I have been constantly frustrated by the absence of any abnormal findings on conventional medical tests over the years. After all, if the standard lab tests are normal there can't possibly be anything wrong with us in the eyes of the average doctor - or perhaps we are just too difficult to deal with.
Recently however something significant did show up in some routine blood tests I had carried out by my GP. Ultimately however I once again ended up frustrated at the medical system here in the UK.
I had attended the doctor's surgery in an effort to obtain some form of evidence for the long-standing liver impairment I know to be present from my symptoms and various functional testing I have had carried out privately (e.g. detoxification profiles, toxic exposure profiles, intestinal permeability assessment etc). I described my symptoms of chronic, dull pain just under my rib cage on the right hand side, intestinal pain on passing stools, stool colour ranging from white to yellow and orange (not a healthy brown), fatty stools, yellowing of the skin (jaundice) etc. Credit to my GP as he always listens and subsequently examined me which involved palpating (pressing) on my body at various points around the liver, gallbladder and intestines. I indicated that the most pain was felt the close he pressed to the liver and gallbladder area. He subsequently ordered a standard liver enzyme blood test - the results of which came back well within normal ranges. Nothing I hadn't expected as low grade liver impairment and inflammation just won't show up on these tests - they look for enzymes released by hepatocytes (liver cells) when they die so only show up when major damage is currently being done to the liver as in alcoholic liver disease or viral hepatitis.
However, my GP also ordered a full blood count as a matter of routine and lo and behold it came back with findings that could not be ignored - my total leukocyte (white blood cell) count was officially low as were numbers of neutrophils and monocytes (vital players in the innate immune response - our first line of defence against infectious disease) and lymphocytes (white blood cells involved in acquired immunity that recognises and attacks specific targets). Here are those results:
On previous blood counts over the past 10-15 years all these results had been hovering just inside the bottom of the 'normal' range so no notice had been taken. This was the first time there had been obvious abnormality and signs of substantial immune impairment so my GP had no choice but to order a retest. Unfortunately, or fortunately depending on how you choose to look at it, the second set of results put me back just within normal range so no further action has been taken.
Now at this point I'd just like to point out what a great example this is of medicine not following the basic principles of science and being more concerned with finances and resources than the health of patients. Put simply I had two blood counts, one showed undeniably low leukocytes and one showed borderline levels. Now how can you make a decision not to take further action when you have one abnormal and one normal (just) result to work from? Not to beat about the bush - you can't! Scientists repeat tests over and over so they can see patterns in results. At the very least a doctor would need a third test to make any kind of reasonable decision about the status of my leukocytes and my immune system. Unfortunately that is not how things work within the National Health Service (NHS) in the UK and most conventional medical systems around the world. A test is just a snapshot - if blood was taken again today my results may very well be low again.
So what could have caused my leukocytes to be low on the first blood count? Well as I've just touched on a blood test is just a snapshot at a particular time and everything in the human body tends to show some natural variation throughout the day and night (diurnally) and over longer periods such as seasons. This is particularly true when you have a chronic illness such as ME/CFS. It may be that I have had low leukocytes on many occassions and this is just the first time it has coincided with me having a blood test. However, there are a couple of factors that immediately spring to mind that I think may account for the result at this time - stress and sugar.
As some regular readers will know, I am currently completing a bachelors degree in nutritional health and at the time of the test I was hugely stressed with writing my dissertation and another essay. This towards the end of a demanding final year with a lot of other work already having taken a lot out of me. My stress levels had also recently been chronically high due to ongoing problems with keeping this website online and running smoothly!
Stress is a factor that should not be dismissed in any disease. Over the past century scientists have gradually unravelled the links between stress and disease. Pioneers such as Hans Seyle in the 1950s showed how the body responds to stressful events by triggering the release of adrenal hormones, adrenaline and noradrenaline in the short-term and cortisol in the longer-term. With the advent of the branch of medicine known as psychoneuroimmunology it has now been established that each system within the body (immune, endocrine, nervous etc) rather than acting independently is in constant bidirectional communication with each of the other systems. As such stress is perceived by the brain/nervous system, which tells the endocrine to secrete various hormones, which bind with receptors on immune cells and direct its action. Unfortunately it is now established that chronic stress through the actions of cortisol and other hormones and hormone-like chemicals (neuropeptides) has the effect of suppressing immunity.
Other factors such as the food we eat can also significantly impact immunity. One dietary component which is particularly detrimental to the immune system is sugar. Unfortunately during the writing of my dissertation I was in the situation where I either had to give up or rely on a regular sugar fix (mainly from sugary drinks) to keep my brain working and my energy levels up. Ironic I know given my medical conditions and the fact I am studying nutrition - but having tried various more natural solutions to limited effect I was left with no choice if I was to meet the university's inflexible deadline. Rest assured I would not advise anyone do the same but I am extremely stubborn and there was no way I was going to risk my high grade average or drop-out of the course at this late stage! I know I can help myself and others with the knowledge and experience I've gained in the future so I had to get through the course by any means possible. Back to sugar itself - simple sugars in their various forms including glucose, fructose and sucrose have profound effects on leukocytes and immunity. The vast majority of various sugars from the diet are converted to glucose in the body - glucose being the type of sugar in the blood that is primarily used as fuel for the cells. Eating a diet high in sugar leads to high blood glucose levels which in turn increases the production of free radicals and other damaging chemicals such as advanced glycation end-products (AGEs) in the body. These chemicals can cause miscommunication between immune cells and the activation of genetic transcription factors such as Nuclear Factor KappaB (NF-KappaB) which has potent effects on immune cells and has been linked to viral infection, inflammatory and autoimmune disease, and cancer. Studies have shown high doses of sugar can reduce the ability of leukocytes to engulf bacteria in a process called 'phagocytosis' by up to 50%.
Stress combined with consuming large amounts of sugar therefore has the potential to lower both numbers of immune cells and their ability to function correctly. I'd urge everyone to look into the effects of stress and sugar consumption on immunity in more detail as it's both a fascinating subject and knowledge we as environmental illness sufferers can use to avoid negative influences on our health.
So, one again, please do not do as I did and take on the amount of work a degree course entails and then resort to sugar to get you through it as I did. I can assure you I am now back to a low carb diet and and meditating more than ever and taking walks in the countryside to manage my stress levels amongst other things!
If you suffer from ME/CFS or other environmental/invisible illness and have had some abnormal test results or you always get normal results despite feeling lousy and would like to vent your frustration please leave a comment below. Also if you'd like to discuss factors that impact on immunity go ahead and leave a comment too...

written by billypil, June 13, 2010
Now I have CAD with CABGs in 1981 and 1997, followed by a TIA during 1981 & a stent in 2007. I suffer from Complex apneas(obstructive & central), multiple bouts of pneumonia plus pseudomonas lung infection, bundled branch block wand now a pacemaker, still with Atrial fibrillation, I have had spinal surgery ( unsuccessful) with metal rods up my spine.
Following my TIA when I drove my car through heavy traffic for 6 or 7 miles without knowing anything about it. I was thought at first to be drunk as I couldn't walk or talk properly. I got over it partly and was told to get safer work, be cause it could happen again. I studied and became a Technical Teacher after I turned 51.
I don't hold oput any hope of being cured now, but I am glad I put up with my problems and didn't stop. One doctor stopped me once and told me I would never get well without stopping, but I only became worse over two years, so I managed to force myself back, into my teaching job and that was the only time missed until I was made redundant July 4 1997. It is my belief that if I had stopped fully, then I would never have started again. I am finding it harder now, as I am having more problems with recall and also stiffening of my whole body.
Perhaps you are different, but I suggest you don't let this thing beat you.
Bill from Australia
written by eva , June 28, 2010
written by Bill P. from Oz, July 06, 2010
I know that over the years I have tried many things, but the only consistant supplement I have taken is Vit E. I don't know if any one has read up on Professor Pall. I think his first name is Martin. I suggest you Google for him and read up on his research suppositions regarding the "Nitrous Oxide cycle". As I am able I am going to find the supplements he suggests and test his theories on myself. What he says certasinly seems to make sense to me. Please tell me if you can't find him and I shall forward information to you. If you do want to contasct me and I am not finding your response my address is billypil@bigpond.net.au, I suggest however that what we do that we also remain in contasct on this forum
Regards
Bill P from Oz
written by Carole Johnson, September 08, 2010
A very frightened Carole
written by Lori, October 16, 2010
Anyway, the last 5 years or so I have been undergoing much stress, family, financial, you name it. I started experiencing weird symptoms like sweating profusely after having my morning coffee or getting really weird dizzy spells after my morning coffee, not to mention ringing in my ears, and seeing light when closing my eyes to sleep at night. I looked these things up and it sent me to adrenal fatigue symptoms. (I worked long hours, 10-12 4 days a week cramming in as much typing as I could, medical transcriber, in order to be considered for my benefits, about 26,000 words a day. It was stressful too).
I picked up some adrenal support and the symptoms sort of went away, and I went on with my daily routine.
I lost my job in February, about 8 months ago and was looking for local jobs where I live, and was offered a scholarship for school. I have been doing school on line, pretty intense, and also still looking for work. I have been under some major stressors again personally too, along with financially.
Anyway, I went to Zumba and I felt fine, was breathing fine when I did the class. Afterwards my blood pressure dropped suddenly and I passed out briefly. My blood pressure has been low since then and my pulse too. I have exhaustion and the light thing at night.
I had previously had blood work for adrenals but nothing came up. Also, of note, my gynecologist put me on thyroid years ago because my hair kept falling out and I was so tired. My lab work showed low whites and reds, I need to find that lab work. Low leukocytes, etc, just as you have spoken of.
Of course, the doctors all think I am crazy, menopausal, or depressed, so I don't even bother going any more.
But, the passing out concerns me. I am a person who doesn't let things get her down, I am definitely not lazy; but, this has gotten me good.
Any advice or thoughts are welcome.
written by HANETTE, March 04, 2011
Appreciate
written by saratronic, March 15, 2011
Haematolgoist did nothing at all and was baffled and just said it was "one of those things". My fibro pain has subsided in the last 6 months although I am still ridiculously tired all of the time. All other tests proved fine except my lungs are not exchanging gases properly and I have developed severe GERD and frequently (once - twice a day) bring food up into my mouth and have a permanent sore throat and bunged up nose.
What is going on? I am in the UK and have found the NHS to be be pants. I have been passed from doc to doc with no diagnosis really, just continuous testing. ANy ideas? Similar stories?
Thanks : ) I still manage to work nearly full time by the way although I was off work for around 6 months at my peak a few years ago! I thought Id never get better but have improved to 75% of what I consider to be "normal"
written by Crystalcr, April 10, 2011
The only symptom I have is fatigue, no other symptoms I am aware of. I have to force myself to get up and do the necessary things in life. I bought vitamins, b12, and recently started drinking zip fizz. I also have very green powder which has superfoods and probiotics. I try and drink that daily. It is a little weird to me that since having low WBL that I would be sick since my immune system is low, well I haven't been sick at all, not even a cold. I have no pain or any other concerns. After reading all your stories I am so praying this doesn't go on much longer. I feel my life is just passing me by slowly by slowly and I am not part of it. Any suggestions would be appreciated? You all have inspired me to get up today and get at least 2 things done.
written by lynlynn, August 30, 2011
So, in my experience, the biggest mistake I made was trying to use medical doctors for this type of illness. Medical doctors lack the training or experience to deal with these long term infections. Medical doctors depend on lab tests, so when you are sick with something that doesn't show up on lab tests, they aren't trained on what to do and often then make mistakes because they try to label you as having something that they were taught about, rather than understanding there are serious illnesses that they don't know anything about. You actually end up sicker for a longer period of time by trying to use medical doctors.
You have to keep searching for alternative medical options until you find something that works for you.
What I found with a Chinese medicine expert is that they are trained to understand how your body is or isn't functioning without much dependency on lab testing. So they can treat these complex infections that doctors can't. They try to get your body back to a functional healthy state. Think about it. Chinese medicine has been around for centuries, long before lab tests. They had to figure out how to treat illnesses without having any lab tests.
I would encourage anyone with a long term illness or infection to find a good Chinese medicine expert and try their recommended treatments for six months or so and see if it helps. I was so far gone by the time I started, it took about 6 months to recover from the long term infection.
The biggest problem we, the people who suffer from these long term infections and illnesses, have is that we tend to have the same mentality as medical doctors in thinking that treating illness is about lab testing and taking drugs. It isn't, and it doesn't work, and it can make you sicker. Try alternative medicine, such as Chinese. And take nutritioinal supplements and do everything you can to get your immune system to function well. This isn't stuff a medical doctor can do.
written by pratik, December 15, 2011
I have been suffering with bacterial overgrowth issues for the last five years. The Antibiotics and the anti acid treatments and the testing procedures have got to me and I grow more and more impatient everyday.
However, I've tried to avoid the antibiotic and anti acid medication over the years as much as I can. I mostly tried to use alternative meds like homeopathy and other herbal stuff with no better results than the the antibiotics. My blood work on the contrary always brings up that my WBC count is usually on the higher side. I am pretty much as stressed as anyone else who is trying to live a normal life and fight the stomach trouble at the same time and I also suffer from food allergies due to mal-absorption and stress. Till the last year, my wbc count was usually closer to the higher 11000 mark..it would range from 8500 to 10000..but this year..it went up to 13400 which is causing me great concern. All the people who've posted stuff on this page say that there's a drop in their wbc which makes me feel more concerned. My doctor tells me that the higher wbc is indicating the body's response to allergies and the infection cause by bacterial overgrowth and intestinal distention..I am a little worried since our problems seem similar but the body's response is not quite the same as yours. I am worried and I hope to get through these problems soon enough and wish all the others suffering with all this wierdness and running around the doctors the same.
written by Tonja, February 26, 2012
Anyway, just thought I'd share
WBC results below - I've always been on the low range of everything.. first time neutrophils went to 1.3 (were 2.1 last time)
Component Neutrophils %, automated count
Your result 38
Standard range 41 - 81
Units %
Component Lymphocytes %, automated count
Your result 45
Standard range 13 - 46
Units %
Component Monos %, auto
Your result 12
Standard range 4 - 12
Units %
Component Eosinophils %, automated count
Your result 3
Standard range 0 - 4
Units %
Component Basophils %, automated count
Your result 2
Standard range 0 - 1
Units %
Component Neutrophils auto count
Your result 1.3
Standard range 2.1 - 7.7
Units K/uL
written by jackdaw, May 12, 2012
Thanks





I read with much interest about your low white blood cell count.I have been "diagnosed" with that and scared by Dr. saying things like - bone marrow test - which I know from one of my sons is very painful as he had one.
I was put into hospital and given so many blood tests, CT scan, chest xray, and a visit to a haematologist - nothing showed up.
So my Dr. now says I am a cunundrum!! Isn't that the most awful feeling, that I think He thinks I am making it all up.
You have encouraged and helped me tremendously.
Recently I went to a Naturopath who asseses people by a Live blood sample with the simple prick of a finger.
He explained to me that I have leaky gut, I even saw a worm like object wriggling around - so here my problem was solved.
I now know why I had been so tired, no energy, depressed, sore
joints and so it goes on.
I am now feeling so much better after him giving me vitamin B12 by injection there and then, and have had 2 weeks on the tablets and powders.
I am really interested in your studies on nutrition and would love to keep in touch regarding diet etc.
My husband and I eat a raw salad every day, rolled oates for breakfast with lecithin and LSA mix, and we use the a2 milk.
I have pulses and vegetable soup most every night but would love to hear if there is anything else we can add to make our meals variable.
Thankyou again, Fay Wilson.
What an amazing thing -