Chronic Fatigue/Fibromyalgia Finally Classified as Autoimmune!

Chronic Fatigue/Fibromyalgia Finally Classified as Autoimmune! post image

When I first started practicing, the medical community did not recognize chronic fatigue. They told patients, it’s all in your head. As nutritionists/chiropractors, of course we helped patients with adjustments and good nutrition and helped them realize they were not crazy. Now, not only is the syndrome and all its corresponding symptoms recognized, it has been reclassified as an autoimmune disease!

Also known as Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS), as well as Chronic Fatigue Immune Dysfunction Syndrome (CFIDS), there have been recommendations for yet another name change to Systemic Exertion Intolerance Disease (SEID), with better established diagnostic criteria, by the Institute of Medicine in a report in 2015.

What is Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS)?

It is a compilation of various symptoms commonly reported as post-exertional malaise (PEM), unrefreshing sleep, concentration problems and muscle pain that typically lasts at least six months. Most folks with this problem have it for years.

Back in the early 2000’s it wasn’t taken seriously and patients found themselves going from one doctor to another trying to find answers.

Patients complained of unrelenting fatigue especially after any kind of activity. There was also the pain – unrelenting muscle pain in various parts of the body. I remember one patient who had MRIs of every part of his body trying to find out where the pain was coming from.

Sadly, they missed the key area of origin – the immune system and the brain. Back then we didn’t have the scanning technology we have today.

Thankfully today we have evidence that this disorder is not all in the head at all.

Well, it is a little.

Structural Differences in the Brain in Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS)

This study published in the journal Radiology, found structural abnormalities in the brains of people with CFS using MRI scans. The imaging showed several crucial differences in the brains of the CFS and control participants.

People with CFS had a slightly lower volume of white matter, which connects regions of gray matter in the brain. They also had very high fractional anisotropy (FA) values, a measurement of water diffusion, in a specific white matter tract of the brain called the right arcuate fasciculus.

Another abnormality appeared in the cortex – an area of the brain that connects to the right arcuate fasciculus. In CFS patients the cortex was thicker than in the brains of the control participants.

According to the reserachers, these structural differences could indicate brain inflammation.

Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS) is an Immune Disease

Researchers at Columbia University’s Mailman School of Public Health have found that ME is a physical disease that may be triggered by an infection and in susceptible people, linger on as a hyper-stimulated  immune response and become autoimmune.

This study, published in the journal Science Advances, involved analyzing the blood plasma samples of 298 CFS patients and 348 people without the disease.

The researchers found distinct physical biomarkers in the immune system of those with the disease. The researchers also found differences in those who have had the disease for less than three years and those who have had it more than three years.

Those who had the disease for less than three years had higher amounts of different types of inflammatory cytokines such as interleukin-17A.

High levels of interleukin-17A are associated with many chronic inflammatory conditions, such as multiple sclerosis, psoriasis, and rheumatoid arthritis.

These seemingly unrelated diseases – neurological, skin and joint diseases are in fact all autoimmune.  Autoimmunity is really one disease process, but may be expressed in many different tissues and systems in the body.

People with autoimmunity commonly complain about chronic fatigue. With these study results we are able to connect the dots and help people more completely.

Big Pharma is jumping on these discoveries with more biologic treatments. These biologic drugs may help some folks but have some pretty serious side effects and are very costly.

These two important studies have brought us much further along in our understanding of ME and CFS. Now that it is classified as an autoimmune disease we can forge ahead with natural treatments that can help turn down the inflammation.

Natural Treatments for Autoimmunity Based in the 4R Approach

  • Remove – gluten, dairy, egg, nuts and other potential allergens, as well as aspirin, NSAIDS
  • Replace – support function in the digestive tract with enzymes and HCl if needed
  • Reinoculate – the bowel with prebiotics and probiotics and a diet that includes resistant starch
  • Repair – the gut mucosa with gelatin rich bone broths, L-glutamine and other nutrients

This approach attempts to uncover the actual cause and imbalances in each individual rather than simply putting a bandaid on the symptoms. Each individual has their own set of imbalances and this needs to be corrected in a specific and individual way. Using conventional medicines that suppress the symptoms may be necessary alongside the integrative functional approach while healing is going on.

More and more there are chiropractors, naturopaths and functional medicine doctors that take this approach. As always, never change your diet, medicines or supplements without involving your health care provider.

See more of my disclaimer here.

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Leave a Comment

  • jmr March 26, 2016, 6:57 pm

    Interesting. I wonder how many decades it will take before your average doctor will accept this. As of 4 years ago, I was still being told by doctors in Ohio at both OSU and The Cleveland Clinic that neither CFS nor Fibromyalgia exist. I now live in a city where there is widespread belief in their existence and see a doctor who believes they are autoimmune.

    Reply
    • Jill March 27, 2016, 8:17 pm

      Hi jmr,
      I’m so glad you are living in a better place where your issues can be addressed. It’s tragic for so many people who are still being told it is in their head.

      Reply
  • Ziva Milczewski March 28, 2016, 3:43 pm

    Hi. I was wondering if you can get the brain or plasma scans on health insurance?

    Reply
  • Jen June 17, 2016, 4:18 am

    How can we get help locating a Dr when an truly help!! I have a functional Dr who only makes blanket suggestions….but really doesn’t test or see the true picture. I’m in the Southern NH area..1 hr from Boston.

    Reply
    • Jill June 17, 2016, 6:47 pm

      Hi Jen,
      Perhaps you could google functional medicine doctors in your area.

      Reply
  • Karina July 20, 2016, 11:40 am

    My “CFS/Fibromyalgia” ended up being Lyme disease + coinfections. I know many others in the same situation. There is a new and supposedly quite accurate urine test out for Lyme borreliosis, so that may give some hope of correct diagnosis and treatment to people who have been suffering a long time. Get tested! Save yourself years of agony.

    Reply
    • Jill July 20, 2016, 3:22 pm

      Hi Karina,
      Thanks for sharing! hope you are feeling better!

      Reply