You got a problem, thyroid?

It’s never a good thing to be told that you have a condition called “Grave’s Disease” – it’s a rather discouraging term. A disease of any kind is far from ideal, and especially not when it is referred to as 6-feet under…

Even more so when you don’t know what it means, and even more so than that when you have barely left your teens and are far too busy enjoying a busy social life.

This blog post is incredibly important and sensitive to me, with some detail not even my nearest and dearest are aware of, and I’d like to share with you a short-film that I filmed last year for the British Thyroid Foundation…

It took a lot of thought to agree to take part but it is for a much needed awareness campaign and for a medical charity with a direct personal connection. How could I say no?

Please share my story to those who may be able to seek comfort from it, and I’m of course happy to speak to anyone that wants reaching out to – just leave feedback at the end of this blog post or click here to send me a confidential email.

HERE GOES!! Eek!  *Bites knuckles”

Click HERE to view my 5-minute story, or copy and paste the YouTube link below in to a new window (PLEASE also read my story below):


To view more patient journeys (including mine) as well as an 11-minute film featuring Simon Pearce, a Professor of Endocrinology at Newcastle University, providing useful insight (also featuring yours truly), click here.

Please continue to read my story…

NEVER underestimate the power of the thyroid gland, all that comes with it and the complications it can cause. If you know anyone suffering, don’t ever dismiss, play ignorant or act uncaring.

Yes that includes you, Katie Hopkins, with your unprompted tweet “My local under/overactive thyroid self-help group meets in KFC.” Grrrrr…

It’s not about being fat or thin – and if that’s all you believe then you ‘gotta lotta’ learning to do! (Especially if you want to be my friend 😉)

The reason why the British Thyroid Foundation wanted to work with me is because I suffered a very rare case. I was incredibly poorly and exceptionally young to have gone through what I did. Although it has taken a bit of time, I have finally turned my life around – enjoying life and a successful career whilst surrounding myself with amazing family and friends. My biggest achievement is completing the London Marathon 2014 (running 26.2 miles non-stop from start to finish), something 8-10 years ago I would NEVER have dreamed of accomplishing.

Photo 13-04-2014 18 38 26 (1)

Pale & shattered but I did it! 26.2 miles!

My story

Nobody in their right minds believes that anything medical is going to happen to them during a stage of life where going out, boys, shopping, Sex & The City and saving up for their first pair of Manolo Blahnik’s were the only things that mattered.

As you can imagine, it was a shock when at just 20 years old I was diagnosed with a rather weird yet severe condition and my immediate reaction was “WTF”, a serious #FML moment. (Though hashtags weren’t a “thing” back in 2004!)

I had heard of a thyroid gland, and my Dad had already developed an underactive one, so I was vaguely aware of the existence of this mysterious gland that lived in ones throat/neck region. But I really did not have an ounce of understanding of its purpose.

Never often needing to drag myself to my GP, my Mum had noticed a change in me and after missing three consecutive periods and not being pregnant (trust me – I did check!), I decided it was time to visit my GP.

Apparently I had a bunch of symptoms, and a blood test form was in my hand within a few minutes of sitting in my doctor’s chair. I passed out at the hospital later that day mid-blood test (I think the worry mixed with the scratchy feeling of a blood test sent me over the edge!).

At 8:30 the very next morning, my mum answered the phone and got me straight out of bed to speak to my GP who was on the other end. I’ll never forget the look of fear on my Mum’s face as she passed the phone to me.

I became instantly hysterical as my doctor began talking, and he asked me to come to the surgery as soon as possible to discuss my blood test that I had less than 24 hours prior. I remember being so distressed, setting my Mum off in to a worried state also. Neither of us knew what was going on but my Mum drove me to the surgery straight away.

I had an overactive thyroid. But not just an overactive thyroid, but an insanely overactive gland to the point that my lack of menstrual cycles indicated my body had literally begun to shut down. Scary ey?

My blood pressure was high too, resulting in an immediate drug concoction of beta blockers and of course the meds to start getting my thyroid to behave.

I remember asking the what, why and how, and being told there is no exact science of why an overactive thyroid occurs. Sometimes it is through shock – such as an accident or pregnancy – or poor immune system – but my case completely baffled every endocrinologist I saw over the coming months.

My GP reassured me saying overactive thyroids are treatable and can be “back to normal” in six weeks. However, to be on the safe side he referred me to the endocrinology unit at the hospital.

I remember texting a handful of friends and some instantly were very excited for me about the fact I was apparently going to become ‘skinny’ (as though that was a good thing?) – I was a size 12 at the time so a little curvy but not enough to get excited about losing weight.

In the defense of these “friends” (some who are off my radar on a permanent basis – fyi), it highlighted the instant lack of understanding about the thyroid gland. When you have a thyroid condition the first thing people always refer to is “is that the one where you lose weight or put on weight?” It’s not anyone’s fault for not knowing, but it still makes my blood boil because it is so much more than that. In fact, I put on weight. I didn’t lose weight with my overactive thyroid which baffled most people I found myself explaining to.

This is such a key reason for why I working with the British Thyroid Foundation. There is such a lack of understanding about the thyroid gland – it is just so soul destroying when people focus on the fat/thin aspect, because I suffered such adverse side effects from treatment because of how extreme my case was.

Six weeks passed and I had made no progress. For the next 18 months I was passed along many endocrinologists and had countless blood tests every few weeks.

Treatment wasn’t working and having seen top thyroid specialists throughout the process, no one knew what to do with me and my health was now at severe risk.

By this point I had gained four stone in weight from the drugs. I had lost a lot of hair – my hair thinned drastically. My eyes had also started to protrude. My head was constantly fuzzy and I felt as though I had flu-like symptoms all the time. My neck felt so puffy too. My heart felt like it was constantly racing and my hands were always shaking.

Regarding my weight, hair, eyes, broken nails, poor skin etc, I remember asking so many questions about what I could to help – but I could never get a straight answer. Everything was about trial and error, which was draining.

There was a lack of care for side effects throughout the process and I was exhausted from the amount of time I was in clinic and even the frequent blood tests were p*ssing me off. I had spent a lot of money on prescriptions too (because hyperthyroidism is technically a temporary condition and doesn’t warrant free prescriptions on the NHS).

Having progressed my marketing career in to magazine publishing I was determined to not let my health get in the way of that. Working in those fashion-led environments full of beautiful people was not a confidence booster.

My confidence deteriorated from how I looked in the mirror. Friends and family may now recall that I barely surfaced for a year or so. There were only a handful of friends I’d be willing to see socially, and I would fret about any large social gatherings I’d have to attend. I felt low that so much time had gone by and my body was still trying to run itself in to the ground. By now I hated the world of science and medicine.

The only solution left on offer, seeing as my health was now at great risk, was to remove or kill off my thyroid gland completely.

I was offered surgery, but I opted for the radioactive iodine treatment instead, which was quite a scary option seeing as I had to be in isolation for a week, and have a whole list of do’s and don’ts such as to not wash my clothes in the same wash as my Mum’s clothes, or wash up my cutlery in the same dish water as hers, or go near children etc. I couldn’t come in close contact with anyone, let alone sleep in the same bed as anyone else.

It was also very weird (and funny to some) that I had to carry a card in my purse to confirm I had received radioactive treatment, in case I set off any security alarms, especially at airports. How embarrassing would THAT have been?!

The next 6 months or so was still a game of trial and error, now that my thyroid gland was slowly dying. I had to start taking thyroxine to make up for that hormone I producing less and less of.

Every 4-6 weeks I was monitored, and saw my thyroxine dosage prescription gradually increase every visit, until I was allowed to take the maximum – proving that my thyroid gland was no longer active.

I instantly felt better. My fuzzy head cleared, my eyes no longer protruded and other side effects started to subside.

When my levels were balanced, I showed signs of being able to lose weight, to which I then pro-actively began a realistic diet and exercise regime. As the weight dropped, my confidence grew. I continued to look after myself, managing to lose all of the weight I had gained – a total of four stone (Yikes!)

I felt like a new person. I was happy again, and my skin, hair, nails etc all improved. I enjoyed a new lease of life. I enjoyed socialising, holidays, shopping for fashion – all the things I loved before.

I now have the function of someone that has an underactive thyroid, because I don’t have a working gland to produce any level of thyroxine, meaning I have gone from one extreme to the next.

There are days where I feel sluggish and very tired, and days where my body just doesn’t want to function.

The best advice I can give any fellow thyroid sufferer (for both mind and body), is to maintain a busy schedule (work AND play!) to keep your brain ticking and your body energised. Look after yourself as best as you can – even if it means getting up 10 minutes earlier to walk to your office instead of getting the tube or bus. Surround yourself with those that best inspire you.

I would be lying if I say it wasn’t hard to maintain a healthy weight. I do have to work harder than others to keep fit and healthy – so I exercise as much as I can, I look after my skin and I have started to follow many food bloggers, finding recipes and foods that are not just about weight control, but are full of nutrients and good for our bodies – for example I eat a lot of bananas and I include pumpkin seeds on so many of my meals – including homemade muesli, salads and cakes. I have learned to find foods that provide me with what my body needs, as a result of not having a working thyroid gland.

I bet most of my friends and family forget that I’ll always struggle to shift the Christmas half stone – because for a few years now I’m in a stable place where my thyroid – or lack of – won’t affect my health or be a conversation point anymore.

For those of you suffering with any thyroid condition, at any stage, please don’t give up. I promise you that once your body finds its happy medium, you will feel better in yourself and will have a positive outlook on life. It just takes a bit of time, some trial and error and the occasional early night to ensure you get in enough beauty sleep. 😉

And who knows – you may someday run a marathon – like I did in London last year. A grueling challenge I never thought I’d do but is by far the biggest achievement of my life. Ten years ago I would never have believed I could be here now happily clutching on to my London Marathon 2014 medal.

Here is a brief science lesson, for those of you need a little level of understanding…

Your thyroid gland produces hormones that control every single cell in your body.

If you produce too much hormone (overactive thyroid or hyperthyroidism) your body is over working itself – increasing metabolic rate and blood pressure. If you imagine everything over-working itself (i.e. symptoms can include weight loss, regular/loose bowel movements, feeling hot etc) until your body eventually gives up from the pressure. Overactive thyroid glands can sort themselves out (with the help of a few weeks of meds) but sometimes they don’t, as per my experience.

On the other hand, an underactive thyroid (hypothyroidism), does the exact opposite – it slows everything down because it isn’t producing enough hormones. Your metabolic rate is slow, your blood pressure is low, and the side effects can include feeling tired, sluggish, finding it easy to gain weight, feeling cold etc. Although thyroxine helps to replace the missing hormones, lifestyle choices can certainly help as I have previously mentioned.

As I have said, this is a very personal subject to me, but one I have chosen to share with you as a result of my short film. If I can help or inspire at least one other thyroid sufferer out there, then I can be assured taking part in the British Thyroid Foundation short-documentary was a good decision.

Please do not hesitate to share my story or video with anyone you know who could be suffering with a thyroid condition. I’m more than happy to be reached out to for confidential conversation – even if it is to recommend food blogs or for general thyroid chit chat. 🙂

Thank you for reading, and thank you for watching.


For more information about all things thyroid, and to view films about other thyroid conditions please visit

Nothing is impossible


22 thoughts on “You got a problem, thyroid?

  1. Vivienne Lewis says:

    Well said Camilla, I remember you at that time. You have come through a difficult time, but you show us how we too can survive. I do mean survivie, because at some point in our journey to a healthy balanced thyroid we all feel that we won’t. My story is different to yours. I visited my GP for some totally unrelated problem. While chatting she said I know you came for something else, but I would like to have your Thyroid scanned. I was surprised although my good friend, an Optician had said several times during an examination that I should have my Thyroid checked. Results always came back as fine. I had the scan, then they did a needle biopsy (not as painful as it sounds) . The result was pre Cancer cells. I had to have it removed and quickly. That was 7 yrs ago. I still have problems. Hair, skin, weight and bowel . The drugs are constantly being changed. I am always tired. Unless you suffer from this condition no one will understand. Good luck to all youThyroid sufferers. If you think you have a problem keep on getting Thyroid checked. You know your body best. Love xxxx

    Liked by 1 person

    • flamingomonroe says:

      Thank you for leaving such a thoughtful comment. I couldn’t agree more – the thyroid is often talked about but there’s a lack of understanding. We have to listen to our bodies and it can take time to get our body happy again. So much awareness work needs to be done and I thank you so much for your love and support. xxxxx


  2. Katie says:

    You are an inspiration Camilla. It’s one thing to have strength and overcome things in life but to really conquer these things takes something special. You, have that. By speaking up and showing what can be achieved you will hopefully inspire those that need to find the something special. I hope I have been a support in the past, and I will continue to be one always. Love you to the moon and back Eddie xxxx

    Liked by 1 person

  3. Kirsty says:

    I’m 5 months post total thyroidectomy and 3 months post radioactive iodine for papillary thyroid cancer. This post was exactly what I needed to read.

    I’m still extremely fatigued and have gained so much weight, and still in the process of getting the meds at the right place. Of course I’m extremely lucky and grateful that I’m only a step away from the cancer being gone and that I’m still here. But I still feel sad about what I’ve lost in the process (or gained, in the case of the 3 extra stones I’m carrying!). Your story reminds me theres light at the end of the tunnel. I identify completely with your feelings of wanting to hide away. I’m glad to know it gets better.

    Thank you for inspiring me!

    Liked by 1 person

    • flamingomonroe says:

      Dear Kirsty. Thank you so much for your message. It certainly sounds like you have been through a challenging time. You sound incredibly brave too. You inspire me! There is indeed light at the end of the tunnel, just stick at it and you’ll get there. Please message me anytime you’d like to or to let me know how you are getting on 🙂 xx


  4. Stella Aquino says:

    Hi! Your post has inspired me a lot, thanks for sharing!
    I myself suffer from hypothyroidism… But for the last 5 years there has been no trends, so it either was too high or too low. Ever since I moved to London, it went back to almost normal, almost hypo but not quite. I do blood tests every 3 months, now every 6 months. I refuse to take treatments so I just keep busy and try to have a healthy lifestyle just as you described. I hate people when they say they are tired because they have no idea! Thanks so much for sharing

    Liked by 1 person

    • flamingomonroe says:

      Wow thank you so much for your lovely comment. I would love to learn what you do, so that you don’t have to take any treatment at all? And what your doctor feels about it? I completely agree with you – some people have no idea. Friday just gone I had 12 hours sleep solid! The more awareness we do the more people will understand. xx


      • Stella Aquino says:

        Welcome:) Well, it’s like you. I keep active and have a balanced diet. I need 8 to 10 hours of sleep but only get them on the weekends… I get regularly tested… Doctors in London seem to think I worry too much :s

        Liked by 1 person

  5. Ninni says:

    Wonderful article. Have you been following Stop the Thyroid Madness protocol? Your blog was posted on one of their private fb pages. After reading the comments, some of your readers could really benefit from checking it out, especially those who are still dealing with hypothyroid symptoms.

    Liked by 1 person

    • flamingomonroe says:

      Hi Ninni – thank you for your kind words. I’d love to reach out to anyone I can help or share my article with whoever you feel can benefit. And I also have lots of followers who can benefit from other sites and groups. I’d really appreciate if you could email me via my contact form with more details. x


  6. Teresa Lindholm says:

    What you are doing is so important, spreading information about the thyroid! 😊 Thank you! I will be showing all material to my daughter Julia 15 yrs, who got the diagnosis autoimmune thyreoiditis a year ago. First she was hyper-, but it soon turned into hypo-. She has been taking thyroxin for almost a year and at first it seemed to work well. During the summer she has had ups and downs…we’ll see how things develop. Really good for her to read about other young women with the same condition! ❤ I wish you all the best in life! Teresa

    Liked by 1 person

  7. Nishita (@nishmvk) says:

    Just found your blog through your Insta and this post really called out to me. I was diagnosed too at 20 with Hashimoto’s thyroiditis. At that time I had put on a lot of weight and was feeling very tired and sluggish. I ignored it because I was in campus and assumed the weight gain was because of poor eating choices.

    It was only when I came back home and seeing how aghast people were at my appearance that I realized something was wrong. Then I started losing feeling in all my limbs…very scary experience. Long story short, I finally hauled myself to the doc and got diagnosed.

    The symptoms are so subtle and creep up on you so slowly. It’s scary. I think now that I must have been suffering for more than a year with these symptoms without realizing.

    Liked by 1 person

    • Flamingo Monroe says:

      Hi Nishita. Thank you for finding me and taking the time to write. I hope you are receiving optimum care and attention during this time. Diagnosis is a big step in itself and you’ll be in my thoughts that you will feel better soon. XCamilla


  8. Meghan says:

    Hi Camilla,

    I just found your blog and I can’t tell you what a relief it’s been to read. I was diagnosed with Graves following a miscarriage this past Christmas. I have no symptoms but due to high antibody counts my doctor recommend that i treat it with RAI or surgery. I’ll be having a total thyroidectomy in 2 weeks as my husband and I don’t want to put off having children for another year. Which leads me to my question, one I hope isn’t too personal, but given that you went from hyper to hypo did you find you had any difficulty in conceiving as a result? Were you on Synthroid or a natural treatment? Any input you might be able to provide would be appreciated – all I seem to be able to find are horror stories on the internet and the ability to start a family has been weighing on us pretty heavily. Thanks!!

    Liked by 1 person

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