Living with Chronic Fatigue Syndrome CFS/ME

I was diagnosed with Chronic Fatigue Syndrome in 2010 after I had been virtually housebound for nearly a year. At the time of diagnosis, and to this day, I felt like it was an unnecessary  and useless label. The diagnosis didn’t come with any kind of treatment plan, medication or even advice. It simply came with a “we don’t know much about it, but you’ll probably have this for life”. I was sent on my way believing that that was my lot. Thanks Doctor.

Chronic Fatigue Syndrome does more then it says on the tin – and that’s why many CFS suffers are fed up with this vague and dismissible name. CFS/ME is a complex chronic illness that manifests differently among it’s victims and involves not only debilitating fatigue, but also chronic pain, irritable bowel syndrome (IBS), brain fog, weight loss, fibromyalgia, headaches, nausea, insomnia, muscle weakness and more.  woman-506120_1920

The causes of Chronic Fatigue Syndrome are still debated, despite it being reported for more than 200 years. It’s likely that there are several triggers, and that a unique mix of factors trigger each individual’s illness.

In addition to viruses as the cause e.g. Epstein Barr, a recent review proposes a disruption of gut microbiota as a possible cause (Navaneetharaja et al. 2016). Our gut microbiome is so important for our long-term health this proposal doesn’t surprise me at all, and it fits with my experience. Because our gut microbes are so important, whether they are disrupted by a pathogenic virus, poor diet, stress or something else, the knock-on effects can be far reaching.  CFS has also been proposed as an autoimmune disease triggered by gut dysbiosis and disruption of the lining of the gastrointestinal tract (Navaneetharaja et al. 2016).

It’s easy to think that the virus that I caught in Costa Rica in 2009 was the culprit, as many studies show connections between CFS and various viruses, but in reality the virus I caught was the straw that broke the camel’s back. My CFS had been simmering away for a long time – I believe since my mid teens.

For me, I believe my immune system has been operating sub-optimally for a long time. I believe that my CFS is a result of gut dysbiosis and autoimmunity.  I know that when I look after my gut and acknowledge my diagnosed autoimmune disease (Hashimoto’s thyroiditis) my symptoms improve. It’s common to collect autoimmune diseases if you don’t catch them early and work at reducing inflammation.

For years I’d had periods of inexplicable exhaustion. As a child I’d happily curl up anywhere and go to sleep. In the summer holidays I remember systematically sleeping in until 11:30am and being shocked by how tired I was, but I simply couldn’t wake up earlier. I’ve never been sporty or energetic and I know I should be in bed at 9pm. I have been constantly cajoled, pestered and teased into doing things – going for walks, staying up late, going to the pub – when my body is crying out for sleep. At university, during my undergraduate, I had one day of SCUBA diving each week in the winter. I’d suffer severe headaches afterwards and I’d be exhausted the next day, barely able to walk to my lectures. In my early 20s I’d wonder if I’d be able to walk to and from town – just a 20 minute walk – but I was unsure of my strength. I remember catching a cold and being in bed for days, and then unable to walk faster than an 80yr old with a Zimmer frame. It was ridiculous and I remember marvelling at my lack of strength.  Each of these episodes passed and, once they had, I continued on with normal life – after all, all the doctors I saw told me I was normal.

Click —>HERE<— for more health news and coaching offers

The final straw

I got seriously ill in 2009, at the end of my PhD. I’d had several quite stressful years during my PhD, but I’d loved my work and was passionate about producing high quality science. I’d worked hard in a very toxic system with no support. I had my ideas and data stolen, suffered abuse of power, manipulation and sexual harassment – things that are rife in academia. No-one had my back. I didn’t have an academic champion or mentor until it was far too late. This stress during my PhD was definitely a huge contributor to my poor health – and a big factor in distancing myself from academia. But it wasn’t the sole cause of my CFS. Many people unhelpfully told me I’d made myself ill by working too hard. While several studies link perfectionism and CFS (as reviewed by Kempke et al. 2015) this isn’t the full story.

What it CFS feels like

The fatigue is like no other. A total exhaustion that stops you from being able to lift your head off of the pillow, from moving your legs to get out of bed, from standing while the kettle boils or from being able to speak. It prevents you from functioning and makes you pause and question the necessity of every action. The brain fog that goes along with it is nothing short of terrifying. I could no longer rely on my brain. I couldn’t recall dates, times, facts or even names of close friends. I couldn’t problem solve. I couldn’t hold a conversation because I couldn’t follow it or remember what had been said or what I had already asked. It was humiliating and scary. I had terrible IBS and, despite eating three or more main meals in a day, I kept loosing weight. I ate and napped. That was it.

I went from being a competent, independent and reasonably intelligent woman to someone who couldn’t communicate with her friends, didn’t have the energy to read and couldn’t walk to the end of the road. I was by myself all day while my husband was at work. I was lonely and down. I needed to be cared for. I needed someone to shop, cook and clean for me, and my husband became my carer.

broccoli-952532__180Slowly I made myself better by focussing on me and allowing myself to put my health first. I took advice, I listened to my body and I learned to let go of anger. I changed my diet, even though my diet was healthy, and my approach to life. I radically reduced carbohydrates and I cut out gluten. I prioritised my sleep and I stopped using chemicals in my home and on my body.

It took time, but I returned to “normal” – at least I was no longer chronically fatigued and ill. I was different though, but in a good way.

I have to keep on top of it, especially since I also have Hashimoto’s thyroiditis, which shares many of the same symptoms as CFS. When I let my diet slip or if I pack too much in (which is a constant tendency),  I know I’ll pay the price.  It’s all about balance.

Go Gluten Free quickly and easily with my new online package – all the resources you need

Do you suffer from CFS or another debilitating illness? I’d love to hear your story.

I’ll be posting soon about the changes I made that helped me get my energy back, so FOLLOW my blog to make sure you don’t miss out.

Want to start feeling better right now? Check out my Reboot  I’ve packed all my best tips on how to get your health back on track in just 4 short weeks. This online package allows you to find your foundation of good health. It guides you through changes that will have long-lasting effects on your symptoms and overall health in a safe and manageable way.  It’s a great start towards taking control of your health and reaching goals!

For more information or to sign-up —-> CLICK HERE <—–C_14

Make sure you join me on Facebook too. Find me at @carolinescoaching and on Twitter @FlourishCP

All the best,

Caroline

 

Advertisements

Chronic Fatigue- diagnosis to remission

Sometimes I can’t quite believe that I was pretty much housebound for 18 months in my twenties. Other times it seems all too close for comfort. The lack of recognition and respect Chronic Fatigue Syndrome patients receive still astounds me.

For me, like many, it was a long road to a very unsatisfactory diagnosis. For over a decade I told GPs that I was exhausted and not able to keep up with my peers. I told them I felt unwell and that I was worried. I told them I was not depressed. I told them that I was sleeping 12hours a day and was still exhausted. I told them I had to rest for days after exerting myself and that I lacked concentration and motivation. At each and every appointment I was told that my symptoms were vague and non-specific and therefore there was nothing to be done. I was told I needed to socialise less (at a point during my degree that I was a hermit), to get more sleep (more than 12hrs a day?) and that I was probably depressed (maybe, but chicken or egg?).

And so I lived in this state of exhaustion. I resigned myself to it. I thought it was just  the way I am. But I could never fathom how people could just get up and do things, how they could achieve so much. Where did they get the energy? Why couldn’t I do everything? Why wasn’t I “normal”?

Things came to a head when I was writing up my PhD thesis. I’d moved to Costa Rica to write up (well, why not!?) and, within a week of being there, I contracted a really bad stomach virus. I didn’t eat anything apart from watery rice for two weeks. I lost a lot of weight and I simply never recovered my energy.

I was extremely ill. I couldn’t shuffle across the apartment without stopping to rest. I couldn’t stand in the kitchen long enough to boil the kettle. I couldn’t hold my arms above my head for long enough to wash my hair. I had to have a nap after a conversation. I had irritable bowel syndrome. I ached all over – in both muscles and joints. I couldn’t concentrate for more than a nano-second and my memory was atrocious. I was constantly hungry and loosing weight rapidly. One day the world went black and I temporarily lost my vision.

I went from doctor to doctor and had test after test. I gave countless vials of blood and saw a seemingly infinite array of “specialists”, but none could offer me any viable explanation. All told me I was “normal”.

I soon learned that being “normal” in the medical world simply means that the test needed to detect what is wrong hasn’t been discovered yet.  Unfortunately, it seems that most doctors tend to listen more to the lab data than to their patients. Either that or they are unwilling to collaborate and problem-solve with the patient.

I wrote my PhD thesis and planned my wedding – I’m not sure whether this was tenacity or stubbornness, maybe a bit of both. I knew that, like most, my PhD was a huge stressor, and had been for sometime. I knew that I wouldn’t start to get better until I could put it behind me. My decision to persevere and finish my thesis was met with a lot of eyebrow raises and head shaking, but I knew having it hanging over me would be worse in the long run. That was my decision.

Back in Australia, newly married and with my doctorate (cum laude) secured, I was unable to leave the house. My GP finally stuck a label on what I had: Chronic Fatigue Syndrome. She told me there was no cure and that I would likely have it for the rest of my life – that there was nothing I could do.

For me, that meant no career, no kids, virtually no social life and that my new husband would be my carer. Clearly something had to change.

I read and researched CFS, and a friend recommended a local naturopathic doctor. Finally someone who listened to me, who didn’t tell me I was imagining my symptoms or that I was depressed. He is ordered tests and diagnosed me with dysbiosis and intestinal permeability – things that many doctors still deny the existence of despite a wealth of evidence. Together we looked at my diet and lifestyle and I began to make changes. It was slow, and it was hard, but I stuck at it. I designed my own diet, one that suited my needs and took my various nutrient deficiencies into account.

Slowly, I began to get better.

I also took a long hard look at my life, and where, and to whom, I was loosing energy. I realised I wasn’t good at looking after myself and I usually put myself last.

What’s most interesting is that my pre-CFS diet wasn’t “bad”. I’ve always eaten vegetables, nuts and pulses. I hardly ever ate fast or processed foods. I always cooked from scratch and kept myself hydrated. Clearly, a “normal” diet was not ideal for my body and was not going to promote healing and health.

I learned that doctors don’t always know best. That you are the expert of your experience and no-one should try to diminish it. Once you have found someone who will work with you, instead of dictating to you, you’re onto a good thing.

Had I not been told I was “normal” 10 years earlier, maybe the autoimmune storm that seems to be my body’s default status now wouldn’t be raging quite so hard.

After a post-doc in the USA, having a couple of kids and caring for my husband through cancer, I am now help others take control of their health as a Health and Nutrition Coach. I help people with chronic inflammation reduce and eliminate symptoms associated with thyroid disease, type 2 diabetes, inflammatory bowel disease, irritable bowel syndrome and CFS, and weight management through cancer. I always encourage people to discuss our work with their doctor. But it’s amazing how many doctors refuse to listen and instead belittle the huge steps these people are making in taking control of their health.C_14

Symptoms of Hypothyroidism

Sleep has always been an important part of my life, and I’ve been able to sleep in some pretty spectacular situations – from a sun-warmed stone on a mountain top to the bouncing bow of a boat in the cold, driving rain. In hindsight, my ability  – or need- to nod off was probably a symptom of my thyroid disease.

Sign-up to my mailing list

—>HERE<—-

Recently I have met a lot of people with hypothyroidism, or suspect they have it despite their blood work being normal. Many of these people have a long list of symptoms that they have never associated with their thyroid condition and have lived with them for years. They are are used to feeling less than optimal and easily put these, often non-specific, symptoms down to age or lack of sleep.

But what if you could feel better? What if you could get rid of those aches and pains?  Today I want to give you a more comprehensive list (but by no means exhaustive) of the symptoms you may experience with hypothyroidism – there may be more than you may realise.

Chronic symptoms of hypothyroidism can be reduced or eliminated through changes in eating habits and lifestyle.

I’m walking proof of this. I have gone from being bedridden, aching all over and barely able to move to, on the whole, being fully functional!  I still get the odd flare-up, but there is usually a clear cause, such as over working, catching a horrible bug or letting my sugar consumption creep up. When this happens I know I have to go back to basics and “Reboot“, to get back on track. And it works.

If you have hypothyroidism, particularly Hashimoto’s thyroiditis, and suffer from chronic symptoms it’s important you know that they are an indication that your body is not functioning at it’s best. You have those symptoms for a reason.

Masking symptoms with pain killers and supplements without addressing the cause can compromise your long-term health.

Sign-up to my mailing list

—>HERE<—-

If you have these symptoms please know that you can feel better. It may take time. It may take effort, but it is possible! With no help or guidance from medical doctors as to how to manage my diagnoses (first CFS and then Hashimoto’s thyroiditis), just a prescription for Thyroxine, for a long time I thought I was going to be virtually house-bound for the rest of my life. Thank goodness I took control of my health and made the necessary changes to feel better.

I read and researched. I used my background in Immunology to understand the science behind my disease, then I listened to my body and used my knowledge of nutrition to heal and get as healthy as possible.

Here is a list of some of the symptoms you may have, even if you’re taking thyroxine. How many of these do you have?

  • Palpitations
  • Fatigue
  • Slow speech
  • Slow movements
  • Brain fog/confusion/forgetfulness
  • Liver tenderness
  • Insomnia (yes, even with hypothyroidism)
  • Hypoglycaemia
  • Muscle and joint stiffness
  • Fibromyalgia
  • Pins and needles
  • Puffy, itchy, scratchy eyes
  • Puffy hands and feet
  • Cold extremities/ low basal body temperature
  • Irritable Bowel Syndrome (IBS)
  • Tinnitus/hearing problems
  • Restless legs
  • Hair loss
  • Eczema/ dry skin
  • Migraines
  • Blurred vision
  • Anxiety
  • Mood swings
  • Inability to cope with stress

I had more than 75% of these symptoms and I was misdiagnosed for 5 years. Now I live largely symptom free!

Get in touch to hear how we can work together to improve your health and get rid of your symptoms.

One to one coaching not for you? Feel better by Signing up for the Reboot!

If you have some of these symptoms and haven’t got a hypothyroidism diagnosis, then it’s advisable to talk to your doctor. These symptoms don’t mean you DO have hypothyroidism and are not meant for diagnostic purposes. If you are at all concerned about your health, then make an appointment to see your doctor.

I am happy to help you make positive dietary and lifestyle changes alongside your medical doctor.

Take control of your health and feel better!

With warmth,

Caroline x

P.S. Have you signed up to my mailing list? Click here for information and offers straight to your inbox, including FREE Pukka Tea when you register for The Reboot!

P.P.S. Interested in health coaching but not sure what to expect? Have  read of THIS page or send me an email HERE.  You can have a FREE Discovery Session with no obligation to sign-up for coaching. Remember, I can coach you no matter where in the world you are!

The Reboot

It’s officially Springtime! Hooray!

I love Spring – it is so full of colour and hope, especially after a long, grey winter (which they usually are here!). I find this change of season inspiring and optimistic.  After being in hibernation mode for winter,  I’m ready for the gorgeous sunshine we have had in recent days here in Devon – long may it last! It makes me want to grab life with both hands and go out and live it!

If only I had the energy and time (right?)

As you may know, I’ve had my health problems in recent years, and I know what it is like for your brain to want you to do something, but your body to outright refuse. I have been there, held captive by exhaustion and fatigue – willing my eyes to stay open long enough to read a book, or to stay focussed enough to make a serious phone call. Getting myself out of that state required a major Reboot. A focus on myself and my health. Read more about it HERE.

(Are you on my mailing list? Sign up —>HERE<<—)

Even now I know when I have been overdoing it. When I haven’t been getting my 7-9hours of sleep (I have two young kids, so this is pretty much a given), when I have been rushing from A to B and sorting everyone else out.  I notice that I am less focused, tired all the time and readily feel overwhelmed – I’m not functioning my best. I know that I am putting my health second, which is not sustainable and is not a good thing!

To battle tiredness I get tempted by sugary foods and caffeinated drinks to get me through the day. We all know that this is a temporary fix, and it usually leaves me feeling worse, not to mention the longer term consequences. But how many of us get stuck in this cycle?  I know I’m not alone in this!

It is time to break the cycle! Reboot NOW

There is no better time for change than Spring – shake off that winter lethargy and refocus on your health. Feel Better!

Give yourself the best chance at making positive changes and making them stick.

Check out my new health coaching package: The Reboot

Are you ready to have:

  • More energy
  • Better sleep
  • Weight loss
  • Less chronic inflammation
  • More control of your health

And more!

Flyer for web

Are you on my mailing list? Sign up

—>HERE<<—

Get updates, news and offers to your inbox. There’s a lot going on a Flourish – don’t miss out!

My Thyroid Story – Hashimoto’s Thyroiditis

We all have a story – something that has led us to where we are today. My health, and that of those around me, has repeatedly shifted the course of my life, changed my perspective and led to some serious personal development.

I have Hashimoto’s thyroiditis – an autoimmune disease that causes hypothyroidism.

This diagnosis came after I had been gluten-free for about 6 months, having put the family on a gluten-free diet because of symptoms my son had (dry skin patches, distended stomach etc). One day I came across a lonely packet of normal (full of gluten) biscuits. Being human, I couldn’t resist and I tucked into them. The next day my thyroid was the size of a tennis ball (or there abouts!).

Aside from “Gerty the Goiter” I also had or developed these lovely symptoms:

  • Brain fog
  • Fatigue
  • Muscle pain
  • Joint aches and pains
  • Muscle weakness
  • Weight loss
  • Headaches
  • Hair loss
  • Carpel tunnel syndrome

A blood test showed that my Thyroid Stimulatory Hormone (TSH) was ridiculously high at 96 (normal levels are approximately 4). My TSH was so wildly out of range because my immune system had been attacking my thyroid gland and preventing it from producing adequate amounts of the hormone Thyroxine (T4). As a result my pituitary gland was churning out TSH to tell my thyroid to produce more T4, but to no avail. I also tested positive for thyroid auto-antibodies.

Hence, I was diagnosed with Hashimoto’s Thyroiditis. Finally I had a reason for feeling tired and cold my WHOLE life (or at least since I was 15).

So, I was put on Thyroxine (replacement T4 hormone).

It occurred to me prior to taking it that Thyroxine stimulates metabolism. I was already struggling to maintain my body weight and, sure enough, as soon as I took the Thyroxine my body crashed. I became bedridden within 24hours and all my symptoms had worsened – it felt like my Chronic Fatigue Syndrome (CFS) days.

At the time I was caring for our two kids and my husband who had Cancer (read about our Cancer story here), so I simply couldn’t afford to be ill.

I had to take control of my health immediately. I did so by radically, but safely, adjusting my diet and lifestyle. Within two weeks I had more energy than I had had for years and my thyroid/CFS symptoms disappeared.

Looking back, I now know I was right to go to the doctor as a teenager with fatigue, as a student with exhaustion, anxiety and muscle aches and as a post graduate with persistent colds and lethargy. Each and every time I was dismissed as needing more sleep or for just being “a student”. In reality my body was struggling to deal with an autoimmune disease.

I don’t blame the doctors for this. Yes, it’s frustrating, but really it is a reminder that we need to be proactive and tenacious about our health – reconnect with our body, listen when something is wrong and then take action.

I’m being proactive about my health by concentrating on reducing the effects of this incurable disease so that I stay as healthy as possible for as long as possible!

Do you have thyroid issues? What are your symptoms and how do you keep them under control?

 

10 things I learned from Chronic Fatigue Syndrome / ME

I was diagnosed with Chronic Fatigue Syndrome (CFS) or myalgic encephalomyelitis (ME) in 2010.  I had been struggling to function for nearly a year and been told repeatedly that nothing was wrong with me – all tests were normal. I got CFS as I was writing my doctorate thesis and after having a really bad stomach virus that my body simply couldn’t recover from.

I was bedridden and/or housebound on and off for about 18months. I had extreme fatigue, brain fog, headaches, fibromyalgia – muscle aches and pains. I was uncontrollably losing weight, despite a voracious appetite, and my digestive system was playing up. At one point I also lost my vision.

It was a really hard time, though in amongst it all I completed my doctorate (yep, with brain fog…) and got married (albeit in slow motion)!  Despite those achievements, I faced the terrifying possibility that I wouldn’t ever be able to work or to have a family – how could I have kids if my arms were too weak to hold them?

It was time to take control of my health. I slowly managed to get myself functioning again by making significant changes to my diet and lifestyle. I have to keep a close eye on my health, particularly in light of a new diagnosis, but I am now able to have a busy, full life and I have two kids (who I can hold, cuddle and run around with!).

Here are 10 things I learned from CFS

  1. We don’t have an infinite supply of energy – diagnosed as a twenty-something this was news to me! It shouldn’t have been – I had spent a lot of my life feeling exhausted, but I had never really acknowledged or accepted it. It wasn’t good enough to be tired all the time – “I shouldn’t need to rest”, “I should keep going”, “naps were a waste of time” etc. I inevitably would pour another coffee or eat something sugary to see me through, then crawl into bed at 9pm.
  2. Energy should be spent wisely – Once you realise you only have a certain amount of energy to spend in a day, and that that amount is somewhat limited, you have no time for people and things that waste it – and that’s ok.
  3. Who gives energy and who takes it away – I realised that I invested a lot of energy into people. When I had CFS those who contributed to my life in some positive way and those who drained my energy became strikingly apparent. This was a really important life lesson. I stopped following-up with the “takers” and I felt immediately better. This was a clear lesson in self preservation.
  4. I am an introvert – and proud! – Despite having a keen interest in psychology, I hadn’t previously dwelt on, or investigated, which area of the various personality continuums I fall into. A very good friend of mine recommended I read “The Introvert Advantage”, by Marti Olsen Laney. For me it was life changing! I strongly related to this description: “Introverts draw energy from their internal world of ideas, emotions and impressions – they are energy conservers”. I realised that I had been living under the guise of an extrovert – perhaps to “fit in” to the extrovert world of science (which is bizarre as many scientists are introverts!).
  5. Physical activity doesn’t have to be high energy – many people with CFS are told that exercise is good – and for some a staged exercise regime works well. For a many years before CFS I would push myself into going to the gym, to swim or go to aerobics classes. In all honesty I hate the gym. I find nothing pleasurable in going at all, and now that makes sense. I much prefer being physically active outside, surrounded by nature or by positive non-judgemental people – its energising. I also realised that I don’t need to keep up with other people’s expectations of what a healthy exercise regime should be – its unique to me.
  6. My biggest energy drains – small talk, rubbish television, sugar, caffeine, anxiety, anger and stress.
  7. My biggest energy sources – one to one conversations with interesting people, time alone being creative and thinking, taking the time to enjoy and savour a really good cup of tea (caffeine-free), yoga, warm and nourishing food.
  8. My body knows what it needs – I just have to listen. For a long time my body had been giving me signs that things were not going well, but I did not acknowledged them. Had I been more connected with they way my body felt, and had a higher respect for it, my dip into the world of CFS may not have been so dramatic.
  9. Epsom salt baths are amazing – I believe everyone can benefit from bathing in Epsom salts! It rebalances magnesium deficiencies, soothes aching muscles, helps with sleep and is thought to encourage the elimination of waste and toxins (sip water while you bathe).
  10. What matters in life – who and what deserves my precious energy. I decided that I deserved my energy – my health was worth fighting for, that I wanted kids and opportunities to live a full life. My kids and family are worth my energy and so are the unique and beautiful people that I am lucky enough to call friends.

This is my experience with Chronic Fatigue Syndrome and I believe it was directly related to my recent Hashimoto’s Thyroiditis diagnosis. Everyone’s is unique – from the triggers to the symptoms and the factors that help or hinder recovery.

Want to regain your energy and take control of your health? Get in touch for a FREE Discovery Session to find out how!

Do you have experience with CFS? Do you know someone with it or who has had it? What did your experience with CFS teach you?

Comment below and don’t forget to Like and Share this if you enjoyed reading it 🙂

10 signs your thyroid is struggling

Tired in bed

It turns out I’ve had an under-active thyroid for the past 17 years. I have Hashimoto’s Thyroiditis, which is an autoimmune disease –  my immune system attacks my body.

Your thyroid is pretty important. It’s responsible for producing hormones that control metabolism, digestion, heart, brain development, muscles… the list goes on and on.  It’s therefore unsurprising that when it goes wrong the list of signs and symptoms is pretty lengthy – and it can be very debilitating.

Like so many people, my signs and symptoms were put down to “being a teenager” then, “being a student” then just “working too hard” or “not getting enough sleep”…

Tired, cold and in pain became my norm.

I wish I’d known about these 10 signs when I was 15:

  1. Fatigue/exhaustion. We’ve all been a bit over tired, but the fatigue I am talking about is on a different lever.
  2.  Anxiety – triple checking the car is locked or suddenly being nervous about leaving the house or driving the car.
  3.  Muscle and joint aches, pain and weakness (fibromyalgia-like)– Oh the pain!
  4.  Scratchy, full and sensitive eyes – Mine felt full of sand and about to pop out.
  5. Brain fog – yep, I had brain fog throughout school, my degree and my PhD – brilliant!
  6. Depression, lack of motivation and difficulty handling emotions – It’s hardly surprising with this list of symptoms, but it is more than that.
  7. Being cold, especially hands and feet – there was a reason I moved to the tropics!
  8. Weight problems – uncontrollable weight gain, or in my case weight loss.
  9. Sleep problems – wakefulness due to anxiety, being wakeful in the night and being unrestored by sleep.
  10. Hair loss and thin, grey hair – beautiful!

This is by no means an exhaustive list of thyroid signs and symptoms.

The good news is that many if not all of these signs can be managed through diet and lifestyle!

I am now fully functional, having been housebound for about 18months a few years back. I’m on thyroxine and I have made some dietary and lifestyle changes that me I no longer have aches and pains and my hair is slowly growing back.

Want some help getting your thyroid under control? Get in touch here for a FREE Discovery Session to find out how I could help you.

What are your thyroid signs and symptoms?

Photo credit: LichtCatchingToby via Foter.com / CC BY-NC