Chronic Fatigue Syndrome and Depression – How Connected Are They?
Feel tired even after you’ve had plenty of sleep? Achy and flu-like even when you aren’t sick? Become exhausted after doing normal, everyday activities that most people can do easily? It’s possible you may have Chronic Fatigue Syndrome.
Also known by its more scientific name, Myalgic Encephalopathy (ME), it’s a condition that has become more widespread in the last few decades. In Britain alone, around 250,000 people are thought to have CFS.
As more research is conducted, interesting connections are being made. One of these is the similarity between chronic fatigue syndrome and clinical depression.
How is chronic fatigue diagnosed?
There is no definite test or result that can prove or disprove a diagnosis of CFS. Instead, a diagnosis is made after other causes of fatigue have been ruled out and symptoms have been present for six months or longer.
Symptoms of chronic fatigue
The National Institute for Health and Care Excellence (NICE) lists the following symptoms:
- muscle pain
- fatigue
- malaise
- disturbed sleep
- concentration issues
Although not official symptoms needed to diagnose CFS, other problems commonly reported by those who suffer from CFS include:
- eye pain
- memory problems
- joint pain
- sore throats and headaches
- tender lymph nodes
- light sensitivity
- problems with bowels
- brain fog
- night sweats
- chills
- issues with standing–dizziness, feeling off-balance
- sensory sensitivities or allergies – bothered by smells or sounds, for example
And then there are the mental health symptoms of chronic fatigue syndrome, which often include:
- depression
- anxiety
- mood swings
- sleep problems
Why are chronic fatigue syndrome and depression so alike?
So alike can chronic fatigue syndrome be to depression, and so often do the two coexist? That chronic fatigue syndrome can often go diagnosed. Ongoing fatigue can affect one’s life to the extent it causes depression, and depression causes fatigue.
Chronic fatigue syndrome and depression present a a ‘chicken or egg’ situation. Did the low moods come first and help cause a diagnosis of CFS? Or are they are result of the physical challenges of CFS making life so difficult moods inevitably drop? It is possible that it is for many a bit of both.
The difference between chronic fatigue syndrome and clinical depression is said to be that those who suffer from CFS do not have thoughts of suicide. That said, those with low levels of ongoing depression don’t necessarily have suicidal thoughts either. So it’s still a blurred boundary between the two.
It is interesting to observe that chronic fatigue syndrome bears more similarities to mental health issues than other medical conditions in that:
- it can be challenging to diagnose
- there is no test to ‘prove’ someone has the condition
- there is no exact symptom list but it varies by individual
- it can make moving forward in life seem more of a challenge
So at the very least, there is something to be learned by looking at the ways mental health issues can be managed and helped if you suffer from CFS.
So I have chronic fatigue syndrome because I am depressed?
There is no definitive answer as yet to what exactly causes CFS, only speculations. Mental health challenges are not the only things thought to be a factor. Other proposed explanations for CFS include: genetics, viruses, hormone imbalances, and immune issues. Research is ongoing, and for most people CFS appears to be caused by a combination of the above.
Isn’t saying CFS is a mental health issue just a way to minimise my condition?
It’s hard enough to have a physical health condition that is not yet fully understood and was not too long ago classified as a “medically unexplained symptom” (MUS).
To be told it’s connected to your mental health can admittedly leave one feeling as if their condition is not been taken seriously, or as if they are being told ‘it’s all in their head’.
Thankfully, in the UK chronic fatigue is now dealt with respect and taken seriously. Although the National Institute for Clinical Excellence (NICE) has of yet not supported the World Health Organization (WHO) classification of CFS as a neurological illness, they do not minimise it into a mental health issue only, either.
Instead NICE states that chronic fatigue syndrome can be “as disabling as multiple sclerosis, systemic lupus erythematosus, rheumatoid arthritis, congestive heart failure and other chronic conditions….CFS/ME places a substantial burden on people with the condition, their families and carers, and hence on society.”
Classifications aside, to ignore the increasing evidence that there is a mental health connection to CFS is to overlook tools and support that, if they can’t make you better, can at least alleviate your suffering.
Proving the link between chronic fatigue and mental health
Research documented by L. Speer in the Journal of Family Practice has yielded interesting information and correlations between CFS and traditional conditions that fall under the umbrella of mental health such as:
1) CFS, major depressive disorder (clinical depression), and somatisation share three physical markers including: biomarkers for inflammation, cell-mediated immune activation, hyperalgesia, and autonomic dysfunction.
2) Two-thirds of patients with CFS may have enough symptoms to warrant a psychiatric disorder diagnosis.
3) Up to 65% of patients with CFS have clinical depression. Although some argue that CFS may cause depression, rates of depression among those with other chronic illnesses are not this high.
Other research shows that clinical depression and CFS may share biochemical pathways that, when activated, damage the body at the cellular level.
Although chronic fatigue syndrome is possibly linked to brain chemistry, it’s still showing up as issues in the same part of the brain that is affected by depression. A study done in Japan that scanned the brains of patients with chronic fatigue syndrome did seem to point to neuro-inflammation as a distinct feature of CFS. But the inflammation was in specific areas of the brain that are commonly linked with depression and thought processes linked to depression.
Other research shows that emotional instability– becoming agitated, stressed, anxious, or excited easily and consistently–has been shown to compromise the immune system and make people more susceptible or prone to all types of disease.
Psychotherapeutic interventions for CFS
Whether or not depression is a cause or symptom of chronic fatigue syndrome, evidence shows that mental health interventions benefit those who suffer from CFS. And are now recommended by the NHS as an integral part of treatment here in the UK.
Cognitive Behavioural Therapy (CBT)
CBT is used to help manage the negative thinking and overwhelming frustration that may accompany a chronic health condition such as CFS and is one of the most recommended interventions.
Mindfulness training
Mindfulness is now showing exciting results for helping sufferers of chronic fatigue syndrome. In conjunction with CBT or other kind of psychotherapy mindfulness can help reduce fatigue and life disruption (read our article about how mindfulness and therapy work together to see how effective this can be).
Even more exciting, mindfulness based cognitive therapy (MBCT) has now been shown to help in cases where CBT fails.
A study carried out by the University of Bath in conjunction with the NHS Foundation trust found that for those who were still experiencing excessive fatigue after undergoing CBT therapy for their CFS, mindfulness based cognitive therapy made a big difference. Participants reported lower levels of tiredness that were still ongoing at a 6- month follow up. They also found that their moods were better, they had more positive thoughts about their fatigue and emotions, and were experiencing greater levels of self-compassion that the control group who did not try mindfulness.
Or another form of talk therapy you like
And if CBT doesn’t work for you and you suffer from chronic fatigue syndrome but don’t fancy trying mindfulness, there’s a good chance another kind of therapy might work for you. CBT isn’t for everyone. Given that all forms of therapy are designed to help clients manage life changes and stress, you might want to look into different, less structured approaches, such as psychodynamic psychotherapy and person centred counselling.
It’s recently been found that managing or preventing CFS is related related to early identification of people who feel and experience stress acutely. According to researchers who studied daily stressors and chronic health conditions, if these people are identified early, “interventions aimed at decreasing reactivity to daily stressors could, therefore, reduce the likelihood that an individual will report experiencing a chronic health condition in the future.”
Counselling and psychotherapy can also help you manage anxiety, deal with the strain having CFS can exert on your relationships, and find new ways to move forward despite their health struggles. It also offers you a safe and supportive environment to air your fears and upsets.
It’s a positive match, not a negative one
It can at first feel defeating to feel physically sick and have someone imply your mental state needs considering. But more and more, healthcare is moving towards a holistic view, and it’s not just CFS that can benefit from considering the mental health side during recovery. For example, Cancer Research UK now recommends mindfulness meditation to sufferers.
As is the case in most life-altering or traumatic events, living with chronic fatigue syndrome is a challenge that nobody asks for. And yet by including mental health care in your treatment plan CFS can offer you the opportunity to reevaluate values and personal identity and potentially experience personal growth.
Do you suffer from chronic fatigue syndrome? Have more questions or want to share a viewpoint? Comment below.
photos by Kristian Bjornard, Antoine K, the Home of Fixers on flickr
I find I really go down hill when it’s my time of the month. I wonder if other ladies see a pattern .
I would imagine yes! Fatigue and low moods are common symptoms. If you find that along with the fatigue you are extremely emotional, depressed enough you push people away, or that you have mood swings to the extent you pick fights with others only to regret it later, do look into premenstrual dysphoric disorder (PMDD). Here’s the NHS’s page on it which is helpful – http://www.webmd.boots.com/mental-health/premenstrual-dysphoric-disorder.
I am not dure of the rhetorik used in this piece, its slightly too ambigously negative in the whole perception of rootcause and effect of mental health allgether and especially in the above presented hierachy/ chicken and egg wuestion here, of the cause and effect dynamic in people with ME/CFS. My moods drastically sink with my energy levels, when my retro virus get re activated snd i have an inflammation burning thru my body; the more exhausted I am the more I feel a profound loss of my ability to manage my life with the necessary activities to manage my mental and emotional wellbeing! I sm plain scared too, how long the flare up will last; I cannot reach out, connect and share how I feel because I live alone. I cant magically get a therapist to talk on the phone or make house visits, I am housebound during flare ups. When I am better, I am out and about a bit, manage my needs, am stable and well mentally and emotionally, I take really good care of myself. I am isolated when I have a flare up when I need support the most and people, including therapists, especially person centred therapists, after CBT was totally unsuitable I did both for a while doing telephone sessions, engage and collude with the repeat symptoms of depression and anxiety and corresponding tjought patterns, not the person suffering from the symptoms. There are no therapists NHS or private, looking at the wole situation of energy mood dynamic and loss of quality of life, social networks, purpose and meaning and providing a stable comfort and reassurance belief and thought framework which replaces societal and human feedback in isolation of chronic illness, necessary for defining an emotional and mentally alternative value to a healthy self. CFS/ME is a chronic illness that causes depression and anxiety through cytokinetic activity/ inflammation and also through the loss of oneself in a society and especially its dedicated health proffessions that cannot respond adequately to the needs of a non functioning member of itself. Referring to Mazlo’s pyramid, one remains on or reverts to the lowest level of human self actualisation, where is the health in that? Yes mindfulnes is good and so is yogic breathing, 7/11, its self care and basic management, not healing or improving.
Hi Sabine, thank you for sharing. We respect your viewpoint and wish you all the best.
I can understand why many people with ME/CFS get depressed – I don’t know about other chronic illness you’re comparing it to: do these other chronic illnesses keep people in bed for long periods, unable to think or move?
What I’m not convinced of is that depression can cause ME/CFS. Do you have evidence for causation? I’m the only person I’ve heard of that suffered with depression, and then as soon as I started to get better I got ME/CFS. My psychotherapist is absolutely convinced that I have ME/CFS because of my family problems, and if things change with my family then my ME/CFS will go away.
I can believe that my immune system was compromised because of high stress, and that could have made me more susceptible to ANY illness. But I just don’t believe that ME/CFS could have spontaneously happened without some external trigger – a virus, or toxins. I don’t believe that ME/CFS is just a different form of depression – because I don’t feel depressed, and I’m not repressing anything now. If this was the same as depression, I would have got better by now.
Nobody actually knows. There just isn’t enough research to yet make any sort of grand conclusion except on a case by case basis. In some cases, for example, CFS occurs after a vaccine. In others just randomly. All that is really sure is that in many cases depression and CFE occur together, are related, and that those with ME/CFS often find therapy helpful. At the very worst it helps with the sheer frustration and monotony the disease itself brings. And fyi, there are many illnesses that do indeed cause people to be bedridden beyond just CFS.Hope that helps. And if you are not happy with your therapist, then seek another you feel more comfortable with. That is your right.
My daughter was recently diagnosed with CFS… This article was very helpful. Thank you. Like you mentioned towards the end of the article, her first complaint, when leaving the doctor was, “why is he worried about my mental health when I am so miserable!”
Thank you for making this information available.
Glad to be of help. Chronic fatigue syndrome is now a recognised medical condition with very real physical symptoms and suffering, but, like many illnesses, mental health is connected. We hope she gets a holistic treatment plan in place soon. Best, HT.
I was diagnosed with M.E/C.F.S in 2014, I have been clinically depressed and I am still being treated for this since 1991, I was 21, I am now 52 year old woman. I have asked for help in so many ways, I have been under the mental health team, a Psychiatrist, I’ve been under the steps for well being and had 2 lots of mindfulness courses, and although helpful to a point, when you have brain fog, forgetfulness and memory loss, these this are only putting a plaster on the problem. I have lived alone in a solitary situation for over 12 years now. I lost my career, my marriage and my friends. I have been and I’m am acutely aware of myself, my illness and my future or lack there of. I have contemplated suicide on a number of occasions. I DO not want to die, of course and I am an extremely strong woman, but there is very little help, ongoing help. You are left to your own devices after the usual treatments and therapies. I don’t have the answers, what I do wish however that this is taken extremely seriously. Who in their right mind would want to live like this. It strips you away bit by bit of everything that makes you, you and left with this empty husk with no ability to contribute to life, to better yourself, to move forward. The world needs to take this very seriously. The only time a mention of this was said, and quickly forgotten again was when long covid effected the many, not us few who live similarly in the background for years. Dr’s know, nothing, no understanding to even show sympathy. No one believes you, as its an “invisible illness” until you take your life. This is just not good enough. I need help, I’m hanging on by my fingernails. Does anyone have anything helpful to add. Before you answer, please do not go through the usual text book therapies etc, I’ve done them all.
I have been diagnosed with: clinical recurrent depressive disorder, Agoraphobia, Panic attacks, Social Anxiety Disorder, Emotional Unstable Personality Disorder, and of course M.E/ CFS. Yet at this moment as I have to do every 3 years is fight my case to the Department of Working Pensions government department to get extra help with Personal Independence Payment, PIP, I’m yet again near the end of a tribunal where they know everything about my personal and medical history and yet the DWP say and I quote ” the letters received from these professionals, do not explain how these health issues effect your day to day living. Physically and Mentally.
Seriously… Letters like this, attitudes like this, are what tip people like me over the edge. They have no concept of the illness or humiliation involved. How can anyone explain tbh unless they live with people like me and see this. These are the things, after all these years are whats important, acceptance of this illness and depression because of it usually go hand in hand, to have it acknowledged as a serious disability as it is crippling and soul destroying. Can anyone help with this. Please.
Caroline