The Reality Of Chronic Migraine – Guest Post by Hannah

Hannah’s guest post is the 10th post in the segment on my blog, called “The Reality Of…” which gives others the ability to share their story and raise awareness of the disabilities, illnesses, impairments and invisible illnesses that they have.

Meet Hannah!

Hannah is the blogger behind Pages, Places, & Plates, a blog dedicated to reading, eating, and travelling. Her passion is sharing her experiences with others and helping them to make the right decision for their next book, food, or travel venture. She lives in Essex, England, on the Sunshine Coast with her partner and her Giant African Millipede.

My Story

I first experienced a migraine at 16 years old on the bus home from school and it really, really hurt. I didn’t understand what it was but presumed it was just a headache, and that perhaps my pain threshold was a bit pathetic.

During my A levels, I experienced them fairly frequently. I’d asked people if they might be migraines but most people reckoned they were just bad headaches – after all, I didn’t lose my vision like one of my classmates, and I wasn’t getting weird spots all over my eyes or throwing up. The symptoms weren’t the classic ones you might expect, so of course it was just me being weak. “Its just a headache” and “You don’t look sick” became phrases I’d hear all too regularly.

Over the years I accepted that they most likely were migraines – the pain was unbearable and occasionally I did experience other side effects, though not regularly. Sometimes I’d feel sick, and other times I might get quite dizzy beforehand. I became a bit more in tune with predicting them… If my speech was slurred, I felt hazy, or even a bit confused then generally it was a sign that a migraine was imminent. They started to affect my studies, and I’d find myself missing out on social events because of the pain.

It wasn’t until I was around 24 that I went to the doctor about it – it sounds silly, but I’d never gone as the attitude of people around me had convinced me that I was a fraud when it came to my self-diagnosis. I guess I also didn’t want to appear weak, but after a three-day migraine that had me clawing at the floor in agony, unable to do anything except lie there desperately trying to remember what it felt like to be pain-free, I realised that a trip to the doctor might not be such a bad idea.

Unsurprisingly, I was diagnosed straight away and given Amitriptyline to take daily to prevent the migraines plus another pill, should I experience the attack. Neither really made a difference and the Amitriptyline gave me some irritating side effects like an unquenchable dry mouth, so I decided to stop the pills and explore other avenues.

By this time, I’d worked out what caused my migraines: bright lights; heat; cold; sudden temperature changes; loud noises; strong smells; stress; not enough sleep; oversleeping; menstruating; being in the sun; screens; exercising; poor diet; lack of caffeine; other illnesses; crying; alcohol; travelling… It goes on. At one point I remember being so frustrated as it seemed everything I did just led back to me lying in a darkened room. Even sleep wouldn’t help sometimes, and the migraine would carry over to the next day.

During stressful times I’d become utterly miserable, usually getting the first signs around lunchtime and having a full-blown migraine by the time I left work. I then wouldn’t be able to de-stress in the evening as I’d have to just go to bed, ready to wake up again the next day to go back to work again… You can see why it could be difficult sometimes. Being a carer for my partner also made it hard and sometimes I’d struggle to juggle work, his mental health, getting household chores done, and looking after my own health.

To combat my migraines, I found that the only thing that really worked medically was Anadin Extra (providing I took them before the migraine hit). I had to get really good at predicting them, but I’d also have to make sure I didn’t take pills too often or they’d become less effective.

I started to really focus on self-care, putting my health as my priority and recognising when I was in a situation that could lead to a migraine attack. I still get them frequently (usually at least once a week) but that’s much better than every day, and only one migraine a month or so will turn into a full-blown attack that incapacitates me. Taking breaks when I need to at work has helped, as well as using blue light filters whenever I’m on a computer or phone and being militant about my self-care regime.

What would really help with my migraines is better understanding from the public – those that haven’t experienced a migraine can sometimes struggle to get why they’re so painful and end up belittling the experiences of those that do (intentionally or not). Had people not played down my experiences I might have sought help earlier, meaning I wouldn’t have spent so many days in agony.

The increasing number of screens in daily life is also making it worse and I don’t think migraine sufferers have really been considered with this – finding a job with limited screen time is difficult in itself (my job can be 7 hours of screen time each day), and now everything else from buying your groceries to checking in at the hospital can involve a screen. Fine for the average person, but when your head feels vulnerable they can be painful, sometimes impossible, to use.

If you know someone who suffers from migraines, be understanding and help them prevent and cure. Saying “it’s just a headache – it will go away eventually” doesn’t help – listen to what they need and provide it. If you’re an employer, understand that your migraine-suffering employees may require a few more breaks, but this is better in the long-run as it helps them be more efficient and stop taking even more time off because they couldn’t prevent the attack.

A little compassion goes a long way and makes it so much easier to treat the issue. I don’t feel guilty or fraudulent when I experience migraines now but I know many people still do, and this is something that really needs to change.

My Favourite Superhero

My favourite superhero is Deadpool! I can totally relate to him using humour to deal with difficult situations (even if underneath he’s actually feeling pretty fragile) and I love how he gets the most he can out of most negative of circumstances. He’s a bit more real than other superheroes to me, and he hasn’t let his superpower abilities change who he really is as a person. Also he’s hilarious!

Thanks Hannah for sharing your story with my readers and me!

If you would like to keep up to date with Hannah, then you can follow her blog, Pages, Places and Plates, on Twitter, Instagram, Facebook and Pinterest!

Posted by

Hey fellow superheroes! I'm Ami, I'm 24 and I live in Norfolk, UK. On my blog, UndercoverSuperhero, I openly talk about my recovery journey which stemmed from being in hospital and a specialist neurological rehabilitation centre for 9 months. I talk about how I maintain a positive mindset whilst coming to terms with my disability. I love superheroes, so much so that my partner and I are having a superhero themed wedding! I generally like to talk about anything and everything on my blog, I also have an ongoing series called "The Reality of..." which allows readers and bloggers to raise awareness of the disabilities, mental illnesses, chronic illnesses, impairments, that they live with as it is so important to raise awareness! Everybody has a voice! 💚

18 thoughts on “The Reality Of Chronic Migraine – Guest Post by Hannah

  1. Thank you Hannah for sharing your story with us and raising awareness about migraines. I have a friend who suffers from them, although not as frequently as you, and it does make her really sick and dizzy. It is unfair how some people just brush off people with migraines as if they don’t matter and that’s why it is so important to raise awareness about them so well done for doing so. I hope the migraines get less frequent as time goes on and wish you well for the future, Hannah. x 🙂

    Liked by 1 person

  2. I had to run out of an exam at uni and throw up in the bathroom. I was found crying on the floor. My boyfriend at the time told me “it’s just a headache”. Thankfully a mate at uni who knew about migraines left him without a leg to stand on. Stay strong. I feel your pain.

    Liked by 1 person

  3. Oh my gosh, this!! I suffer from migraines and while they are not as frequent as yours, they are debilitating. I get a numb tongue and face, my speech slurs and I lose my vision or see spots everywhere. It is terrible. I have even fainted from my migraines and feel so sick to my stomach. No one truly understands just how awful they can be unless they have experienced them. Thank you for sharing x

    Liked by 1 person

  4. Thanks for sharing Ami and Hannah!
    I experience migraines but fortunately not too frequently. My first one was when I was 13 years old and my vision went funny on the way to school and then in my first lesson (RE) my teacher sent me home – with the suggestion that I had a migraine. They went on for a few weeks and then that teacher suggested I get my eyes tested and my prescription doubled in strength :-O

    My GP has never bothered to try to medicate because my attacks are so random – I only get one or two a year. I always get the visual aura though and that is terrifying because I am so scared that I am suddenly losing my sight and am I having a stroke? That it takes me a while to realise that I’m about to have a migraine and I need to make sure I’m at home ready for when it hits.

    I definitely agree that employers could do with listening to staff more – especially those with health issues. It would save so much loss of productivity if they would allow more frequent breaks that would in turn lead to fewer sick days.

    Liked by 1 person

      1. Oh yes – took them completely away for a few years. If I start getting migraines regularly I go and have a check up (even if it’s early) and my prescription almost always needs to be increased, then they settle down again.
        If only it was as easy to solve the random ones that I get once every six months or so that don’t seem to have a cause! I’m just grateful that they are so rare for me xxx

        Liked by 1 person

  5. I think there definitely is more that can be done for migraine sufferers. Like you say, a little compassion goes a long way! I’ve only ever suffered from 2 or 3 thankfully but I wouldn’t wish them on anyone, they’re horrific and it’s so much more than a headache. One or two girls I used to work with suffered with them and they’d just be given no sympathy whatsoever apart from being told to go and have a drink of water and some paracetamol! A really informative post, thanks for sharing 🙂

    Liked by 1 person

  6. Great post. I too have been a sufferer of migraines since adolescence. Thankfully mine are not nearly as frequent although they typically come in clusters (misery loves company). I have tried newer drugs with each evolution of them but still none work consistently. (My wife actually is a neurologist so she is very understanding about them but even she can only do so much for them). I too have found being able to predict them helps somewhat. Having a cancer diagnosis, however, was a rather unhelpful development (imagine that!) as it just raised stress levels to heretofore unattained levels. Anyway, your piece is very important. Thank you for sharing it.

    Liked by 1 person

  7. Thank you Ami and Hannah for sharing your story. I agree it is important to raise awareness so that others do not suffer silently and as you say, those that do not have migraines or understand them can show more compassion.

    Liked by 1 person

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