When no one believes

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A while ago I did a post on how a very British lady called Sarah Colwill developed a Chinese accent after a severe migraine. The post included a reference to how Ms Colwill lost friends because they thought she was pretending (read more here).

At the end of that post, there was a video of two Australian ladies who both developed Irish accents. One of the ladies underwent a brain scan, and the results showed there were some abnormalities with her brain. Poor thing, (at the 14th minute of the episode) she burst into tears – not only was she being told her brain was not normal. Her MAIN REASON for the tears, however, was a strange relief: it was objective proof, after many years of suspicion, that she was not faking.

UGH.

If you’ve ever had migraines, or another chronic pain condition, then the chances are your symptoms are often invisible to others.

Sometimes they might even be intermittent, which means you can be smiling as you walk through the office door in the morning, and then struggling to form a sentence and staggering towards the exit an hour or two later…

I can see how this might look iffy to an outsider… especially an unempathetic, uncurious stranger. And, when I’m super honest, I can admit that even I wasn’t overly sympathetic to other people’s migraines when I was younger. I vividly recall that I assumed another lady was lying about her migraine because she didn’t look “sick enough” based on my personal standards at that time.

[I will never stop apologizing to her, wherever she is, for my ignorance: “I have a migraine” is not a lie.]

Migraine is often referred to as a “bad headache” by those who don’t know better. It’s a casual comment, but it can feel crushingly dismissive to anyone who has experienced the whole-mind-body-soul-catastrophe that is a migraine event.

My bad migraines are hemiplegic, which means I become partially paralyzed down one side of my body. But even that’s not overly obvious to others. The projectile vomiting which should assist in clarifying how sick I am, still isn’t always enough. I remember a stranger telling me it was too early to be drunk (as I was vomiting into a bush thanks to the sudden onset of a migraine while wearing a business suit). Another time, a taxi driver refused me service because he thought I was drug-affected.

Then there’s family and friends. They are generally more patient and understanding, but not always. There’s a whole book that I reviewed that talks about the drama of the “not tonight honey, I have a headache” debacle. Another on migraine survival“, includes the migraine-affected-author explaining how her (ex)boyfriend told her to drive herself home… and her tennis coach called her lazy.

But what about healthcare professionals? Surely they should be the most understanding? Not always. And this dismissiveness takes the distress up a notch. I’ve written before about doctors behaving badly (here) and the ‘Not Tonight’ post included this quote from migraineur Cindy McCain: “The first doctor I went to basically said, ‘Well, you’re just neurotic, you’re just stressed, your husband’s a senator. Go home, put your feet up, and have a drink.’ […] What affected me the most was being talked to like I was dumb. That infuriated me.”

Sigh.

[Oh! And don’t forget the advertising executives! Especially those of the past, who were anything but sympathetic in their sales pitches: Migraines – as advertised.]

My point is: sometimes one of the worst things about being chronically ill is people not believing that you ARE ill.

I’m not alone in this double-discomfort.

Here are three other blog posts I have come across which mirror the emotions beautifully. (Or horribly sadly – depending on how you look at it). Each post deserves to be read in full:

What If – Waltzing With Migraine: “No one wants to hear about your headache. Do you even really have a headache? […] What if they had believed me?”

Fragments from the Migraine Archive | Another Spectrum: “Migraine does not always follow the textbook. […] They speak to the quiet endurance of being disbelieved, the civic cost of diagnostic rigidity, and the emotional labor of explaining what cannot be easily explained. […] they ask, gently but firmly: What if we believed people the first time?

A tough break and a wow moment| painintheBECK: “….I thanked him for believing me & his other patients. When he said, ‘of course I believe you!’ I had to explain how many times a patient like me has to explain and re-explain and advocate for ourselves because doctors do not believe.”

Lastly – a short while ago, a comment was left on a book review, in which Boozilla said this:

Once I was in the ER in a terrible situation, and the nurse said, this is going to hurt. I said, I get migraines. His face drained and he said, OH GOD. That is the gold standard of pain. Then he smiled and said, no worries.

Just like the lady who wept with relief that she had a brain scan to show she was not faking, or the interaction with a medical professional who ‘gets it’, these sorts of moments of recognition are often as fleeting and ephemeral as a flown-feather, but land as heavy as an iron anchor; their resounding thump leaves a migraine-patient feeling seen and heard and understood.

Here’s hoping there are more “I believe you” moments, and a lot less doubt, shoulder shrugs, and “deal with it” comments.

It’s the main reason I keep tippity-tappetty-ing away at my keyboard. I hope I can raise awareness about the nightmares that migraine-peeps go through, so that there will be more empathy and understanding.

I see you.

I get you.

And I’m sending you lots of digital hugs, gentle light and laughter, and healing vibes galore.

Take care taking care, Linda x

*

PS – If you are keen to try to find your own way ahead, improve the way that you can advocate for yourself or improve communications with those around you in general, here’s links to 7 of my prior posts that include some tips and tricks you can try, in alphabetical order (just because):

Be the CEO of your own body

Compassionate communication

Death by papercut (managing micro-aggressions)

How do you respond to pain-ignorance?

Mansplaining migraines (and painsplaining away)

Migraine Love Language

(Un)solicited advice for migraines


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48 responses to “When no one believes”

  1. Lynette d'Arty-Cross Avatar

    Thanks for your very informative post. It’s brutal how often people are not believed when it comes to this medical condition (and many others). I’ve been accused of faking a peanut allergy so I think I get some sense of your situation (I carry an EpiPen). Humans can be so judgmental when they really have no idea and of course it doesn’t help that there are in fact fakers out there, too.

    1. The Mindful Migraine Blog Avatar

      I don’t carry a grudge because I’m a skeptic too (but hopefully not so judgmental!) have a wonderful week xx

  2. James Viscosi Avatar


    You see this a lot too with aneurysms, where people (especially women) present at the emergency department and get told they have exhaustion, dehydration, even migraine, and sent home with painkillers. Sometimes multiple visits are required to receive a proper diagnosis, and delays like that are precisely what you don’t want in that situation. (BTW, the thing that skewed my self-reported pain scale when I was in ICU was the kidney stones, because I kept comparing everything to them. I remember one time I was kinda holding my head and maybe moaning a little and the nurse asked me what my pain was on a scale of 1-10 and I said a three. She was like, “That doesn’t look like a three to me” and went and got me more painkillers. 💊)

    1. The Mindful Migraine Blog Avatar

      I’ve come to the realisation that I might have to tell a fib next time I go to emergency (fingers crossed I don’t have to) and remember to bump up my number to be taken seriously – because once you get chronic migraine, everything starts to feel like a low number, but for the ‘average’ person it would be a lot more… I think kidney stones are meant to be up there on the pain scale… poor you 🙁

  3. The Oceanside Animals Avatar

    Java Bean: “Ayyy, some humans just love to accuse other humans of malingering or faking. Just another reason why having big brains just gets in the way sometimes. If people could just sniff things out like we dogs do, they would understand each other a lot better!”

    1. The Mindful Migraine Blog Avatar

      I read somewhere that some dogs can sniff out illness… so maybe we need a dog at the hospital who does the triage instead of the nurse!

  4. Sarah W Avatar

    Thank you for this post Linda. As someone who experiences migraines and other invisible conditions, not being believed is sadly far too common. My late mother never believed I was ill and as a result, our relationship in the last years of her life was irreparably damaged. Sad really. But I’m so grateful for the blogging community where people generally get what we go through.

    1. The Mindful Migraine Blog Avatar

      💜😔I’m so sorry for the way things unfolded for you, but I too feel blessed that there is a strong community of believers and supporters here… you guys saved me and I feel honoured to be able to repay the digital love back 10-fold xx

  5.  Avatar
    Anonymous

    Excellent post!!! I know from personal experience that it is appalling when medical professionals make light of the pain a patient is describing. (I had migraines many years ago. The doctor I went to was dismissive and useless. However, after doing my own research, it turned out that I needed to be gluten-free in order not to induce migraines. It worked!)

    1. The Mindful Migraine Blog Avatar

      Hooray! 🎉 I love it when people find their own way to health and happiness – of course it’s frustrating not to get the support you need, but it also an act of ultimate empowerment – you’re the CEO of your own body / life, so yay you! 🥳

      1. magickmermaid Avatar

        Thank you! 🙂 (I’m not sure why it says “Anonymous”. It was me. 🙂 )

        1. The Mindful Migraine Blog Avatar

          Ahhh…. that’s just WordPress being wordpressy!

  6. katelon Avatar

    In an ER visit one time, I had one doctor say to the nurse, she’s just faking it to get the drugs, go on and give her the drugs. I reported him. Thankfully I don’t get migraines anymore. But I have great empathy for those with silent illnesses.

    1. The Mindful Migraine Blog Avatar

      Ugh 😣 the “drug seeking” narrative is very strong in Australia, I have been denied treatment twice because the medical examiner decide I could just do with some more sleep rather than risk their license… I get it…. But, when you know you’re sick it’s disappointing not to be heard 😔💜 glad you’re better now, and thank you for taking the time to share your story xx

      1. katelon Avatar

        The good thing that came out of that ER visit, was the rude doctor referring me to a great mind body therapist, thinking it was all in my “head”. The therapist didn’t cure my headaches but he started me on the path of working with great mind/ body holistic therapists.

        1. The Mindful Migraine Blog Avatar

          Wow, great – I had a sort of similar experience with my neurologist that sent me on my whole mindfulness path – I will always be so grateful that I made the pivot; there’s still migraines, but none as bad as before! So glad you found relief to xx

  7. Mary K. Doyle Avatar

    The mind is so fascinating.

    1. The Mindful Migraine Blog Avatar

      It really is 🌟

  8. Gail Perry Avatar

    Having both migraines and a couple of other chronic pain conditions, I have to have a big shout out to the physician who recognised the true extent of migraine pain. After my recent shoulder replacement surgery, my surgeon said that anyone who had suffered chronic shoulder pain prior to surgery would find the surgical pain easier to manage than those who had not. It was his way of recognising the severity of my earlier pain. Now that the shoulder pain is gone (!!), I can begin to search for ways to manage the rest of my chronic problems.

    1. The Mindful Migraine Blog Avatar

      I often wonder if these doctors went through pain themselves, or are they just very empathetic… either way, it feels like a gift when they come along! 💕so glad your shoulder has healed beautifully!

  9.  Avatar
    Anonymous

    Thank you, Linda

    1. The Mindful Migraine Blog Avatar

      My pleasure – hang in there 💕

  10. Dana at Mindful Caravan Avatar

    Thank you for this, Linda. I see your caring through your sharing!

    1. The Mindful Migraine Blog Avatar

      My pleasure – wish it were otherwise for us all, but hopefully the recognition of what people go through helps xx

  11. daylerogers Avatar

    Linda, I’m so sorry for the way you and other migraine sufferers have been treated with such a dismissive attitude and a sense of “you’ll get over it soon enough.” I can’t walk in your shoes, but I can empathize with the massive challenge of what happens when you endure a migraine, not knowing what symptoms will show up. I value your bravery in sharing honestly about the reality of pain. Maybe it’s because it’s easier to marginalize what you’re experiencing that attuning to the pain that is there. I applaud your wisdom and grace in how you share this.

    1. The Mindful Migraine Blog Avatar

      thank you always for being so understanding – I am better than many others I have met; my heart goes out to everyone who finds themselves on the margins!

  12. silverapplequeen Avatar

    Half the time, when I tell people I have a migraine, they think I’m making it up to get out of something I don’t want to do. The other half, they think I have a hangover, although I quit drinking a long time ago.

    If they do believe me, they want to know what I did/ate/where I was that triggered the migraine. So it’s all my fault no matter what.

    1. The Mindful Migraine Blog Avatar

      Ugh – 😣- people often think they’re being curious, but too much of the “did you, can you, why not?” Can be exhausting…

      1. silverapplequeen Avatar

        It’s none of their fucking business.

  13. Susana Cabaço Avatar

    You illustrated well the “pain” of not being heard or believed when the pain and discomfort of migraine are excruciating enough. You are definitely raising awareness on this subject, and I truly enjoy reading from you, Linda! Thank you for being you and for being here! Lots of light and blessings your way, dear friend! Always! ✨🙏💖🌻🌈

    1. The Mindful Migraine Blog Avatar

      Sending love, light and laugher right back to you! xx

  14. Poetry By Maggie Watson Avatar

    Linda you do an amazing job of raising awareness.
    I tip my hat to you.
    As I have mentioned (I don’t get a migraine often now), but there are so many illnesses that are invisible.
    Why would anyone FAKE being sick.
    Wishing you a good week ahead 😘❤️🙏

    1. The Mindful Migraine Blog Avatar

      Look, it blows my mind too that anyone would fake being ill… most people don’t understand invisible illnesses until they get one 😔

      1. Poetry By Maggie Watson Avatar

        Exactly 😪

  15. richardbist Avatar

    It’s sad that some people can’t understand invisible symptoms. How many people die each day due to doctors and specialists not looking deeper, asking more questions, listening a little more intently?

    Migraines are one of those silent illnesses that isn’t understood unless experienced, it seems.

    A good read, Linda. Hope you have a wonderful week ahead. 🙂

  16. Johnbritto Kurusumuthu Avatar

    A deeply moving reminder that not all pain is visible. Being believed can mean so much to someone living with an invisible illness. Your honesty beautifully highlights the need for empathy, patience, and compassion instead of judgment. Sometimes, simply saying “I believe you” can be a powerful act of kindness. ❤️

    1. The Mindful Migraine Blog Avatar

      thank you kindly! I was amazed how many people wrote the same things in their posts; it really is powerful to know that you are seen and heard and understood – thank you for being someone who supports people like us!! 🌟

      1. Johnbritto Kurusumuthu Avatar

        🤝🙌🎉

  17. thomasstigwikman Avatar

    That is a lot of suffering. I am so sorry you have to endure all of this plus people not understanding. About the accents. It is quite difficult to fake an accent in the long. It is funny how people can be so distrusting. I have an accent when I speak English because I am originally from Sweden and I perfected my English as an adult. There’s nothing I can do about my accent and yet people have accused me of faking my accent.

    1. The Mindful Migraine Blog Avatar

      How odd?! I can’t imagine telling anyone that they sounded as if they were faking (even if I was suspicious) – as you said, if your accent is consistent, it’s most likely the real deal… I wonder what people think you stand to gain from faking an accent?? ugh, how frustrating!

      1. thomasstigwikman Avatar

        A lot people mistakenly believe that accents are easy to get rid of or change, but they are not. Arnold Schwarzenegger has been in the US for decades and he can’t get rid of his accent. It is perfectly normal and something you can’t control.

        1. The Mindful Migraine Blog Avatar

          Curious – which language do you dream in?

          1. thomasstigwikman Avatar

            Interesting question. I typcally don’t remember my dreams in great detail but I’ve caught myself speaking both Swedish and English in my dreams.

            1. The Mindful Migraine Blog Avatar

              Ah! Very cool!😎

  18. Darryl B Avatar

    Linda, so sorry you have to deal with this soul-crushing illness day out and day in. I read the other post about advertising…no words 😑

    1. The Mindful Migraine Blog Avatar

      I’m actually feeling so much better these days which makes it easier to handle the strangeness of it all … AND – I can also acknowledge that my life has been so good for so long, I’m #blessed to only find myself on the margins in my 50s. It makes me all the more passionate to help those who have experienced this drama much longer than me! Thanks for being one of the ‘good guys’!!

  19. boozilla Avatar

    SMOOCH..gently of course!

    1. The Mindful Migraine Blog Avatar

      squeezy-hugs right back at you lovely! xx

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