Informational Posts / News

International Women’s Day and How Thyroid Disease is a Feminist Issue

Originally published on 8th March 2018
Last updated on 8th March 2024

The 8th March marks International Women’s Day, commemorating the movement for women’s rights. Hypothyroidism and Hashimoto’s affects a lot more women than men (7-15 times more women), but sadly a lot of women, when they go to the doctor complaining of tiredness, depression, brain fog, memory problems, weight gain etc. are made to feel as if they are hypochondriacs. 

Rachel Struggling With Mental Health Thyroid

Disbelieved Women

Myself and many other women have been made to feel as if we’re making up our complaints of thyroid symptoms or are brushed off with “Well this is all normal for a woman your age”, “It’s all in your head”, “Just eat less and move more”. Read my article about medical gaslighting here.

Middle aged women are especially likely to be told that it’s all normal for someone their age and then sent back out the door with nothing more.

As someone who had symptoms since my teen years, I also experienced difficulties in getting diagnosed and being listened to, as doctor’s felt that I was too young to really be experiencing all the symptoms I said I was (muscle cramps, heavy fatigue, poor stamina, irregular periods, depression, anxiety, acid reflux, brittle nails, aches and pains). I was told that it was ‘all in my head’. It wasn’t.

Men are Believed Over Women

Research indicates that physicians are more likely to interpret men’s symptoms as biological and women’s symptoms as psychosocial. That is, that women’s symptoms are a result of a mental, rather than physical, illness.

Which doesn’t surprise me. But it is still wrong nonetheless.

I have noticed better results when I take my husband with me to a doctor appointment. I find that they’re more receptive to what he has to say about me (even if he’s saying the exact same things I raised with the doctor alone, in a previous appointment), and the doctor has even spoken to my husband directly about me, as if I wasn’t sat in that very room!

What We Feel is Real

Many women are shrugged off, made to feel as if they’re making their symptoms up and then are dismissed for years, before eventually being diagnosed with a thyroid condition. All along they were actually living with a real health condition. It wasn’t just existing in their heads, it was absolutely real. 

It is not ‘normal’, ‘expected’ or has to be ‘put up with’. Hashimoto’s and hypothyroidism  wreak havoc on many peoples’ lives. Mainly women too.

Of the 750 million people living with thyroid disease across the world, as many as 60% are undiagnosed. Are they undiagnosed because doctors are dismissing their concerns and not thinking to run the appropriate tests? Especially with women who they decide to prescribe antidepressants for instead?

The fact that the symptoms are so varying, means it can make it difficult to catch and diagnose the condition, but as so many people have it, it’s obvious that we need more regular screening to get those living with it treated sooner.

We also need more people (especially doctors) to be more aware of thyroid disease’s existence and manifestation, especially in females. Doctors need to be listening to their female patients more closely and not dismiss their concerns just because they’re a woman, and obviously an hypochondriac who’s also probably depressed and loves the attention (note the sarcasm in my voice).

The Risk of Missing That Diagnosis 

Failure to pick up on Hypothyroidism and Hashimoto’s early enough can lead to patients experiencing miscarriages, mental health issues, hair loss, impacts to their relationships, weight fluctuations, loss of ability to do as much as they used to (hobbies, social life, work life, exercising all affected) and even cognitive effects, such as brain fog and experiencing memory issues. Many women are losing years of their life unnecessarily.

What are your thoughts on this topic? Share in the comments below.

You can click on the hyperlinks in the above post to learn more and see references to information given.

About Author

Rachel Hill is the highly ranked and multi-award winning thyroid patient advocate, writer, speaker and author behind The Invisible Hypothyroidism. Her thyroid advocacy work includes writing articles, authoring books, producing her Thyroid Family email newsletters and speaking on podcasts and at events about the many aspects thyroid disease affects and how to overcome these. She is well-recognised as a crucial and influential contributor to the thyroid community and has a large social media presence. Her bestselling books include "Be Your Own Thyroid Advocate" and "You, Me and Hypothyroidism".


  • Irene Forshaw
    March 11, 2022 at 9:56 am

    One of my bitterest thoughts (yes this remains an issue for me) is the sheer waste. Not only to individual lives, mostly women, their partners, their children and dare I say the world. Many women, myself included, have been unable to make the contribution to society we would have wished because of the medics inability to see what they are being presented with by the patient. The perpetuation of the myth of the hysterical women is almost unbelievable; if it was not actually still happening. From an economic point of view, from which everything seems to be calculated these days, it makes less than no sense to misdiagnose such a huge number of individuals. I am assured “It’s very easy (and cheap) to treat” (Ha) but then why is it so difficult to diagnose and so easy to create a living hell for the patient? Frankly I think it borders on criminal. Thank you Rachel for creating a space for the issues you cover. A light at the end of a very long tunnel.

  • Hildur Jónasson
    March 10, 2022 at 10:42 pm

    I had all the classic symptoms for 15 years before I was diagnosed – fatigue, hair loss, constipation, extra weight that wouldn’t budge no matter how I ate/exercised, skin so dry I scratched myself until my skin bled. My doctor prescribed antidepressants and they didn’t seem to do anything. Thankfully I found a doctor who is a MD and practices functional medicine who diagnosed me. It took me 15 years to find a doc who was able to help me. I am now mostly vibrant as long as I stick to a balanced eating/sleeping/exercising/destressing regimen. Don’t lose 15 precious years, educate yourself, demand more from your healthcare provider (all the right tests) or keep searching for a doctor who is up to date on thyroid disease.

  • Hedi
    March 8, 2021 at 10:42 pm

    One of your strongest ones x


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