Headlights For Brain-Fog

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Where I live in Australia, we don’t get fog very often.  Occasionally you’ll see images of the Sydney Opera House on early morning television, with mist rising off the harbor and a notification that the ferries will be cancelled for a couple of hours, but that’s about it.  There is, however, one road between Sydney and a city called Wollongong which regularly gets foggy.  I’m not going to pretend to understand the science of it all, but whatever the required altitude, bowl-shaped-terrain, temperature or humidity is required to make fog, it all seems to condense perfectly right there. 

When I say ‘fog’ I mean that cars on the road slow down a bit, but that’s about it.  Driving visibility isn’t really impacted, its more that the scenery around the car becomes fairytale blurry.

There was one time, however, a few years ago, when I found myself alone in the car as the fog on this road became particularly thick.  It was beginning to be hard to make out the road two or three cars ahead, and it seemed to be getting worse.  I started to stress.  “Sh!t, sh!t, sh!t,” I thought as I tried to remember what I was supposed to do.  Was it turn off your headlights (I think they bounce off the fog and shine back in your eyes?) and turn on your fog-lamps.  That seemed right, but what was the setting for my fog-lamps?  I guessed they were the ones that Sydney-siders use to park in a public garage; small lamps down low that still help you get around the carpark, but not so bright they annoy other drivers.

By the time I had decided this was the way to go, I was struggling to see the car in front of the car in front of me.  “Am I supposed to pull over?” I wondered out loud.  “I’ll have to be quick enough that the car behind me doesn’t hit me, but not too quick because I don’t want to hit the car in front if they have the same idea… sh!t” (there was a lot of swearing going on in this car trip.)  “Maybe I should just stick to a steady pace and keep going, but put on my hazards,” I decided, “but then again, will that make the car behind think I’ve come to a stop?  Will that accidentally set off a chain-reaction of braking???  SH!T!!”

For the life of me, I can’t remember what I decided to do.  I think the car directly in front of me put its hazards on as it slowly kept driving and was swallowed by the dense mist (a bit like it was in a Stephen King horror story), and so I followed suit.

I know that it only lasted a few minutes, the fog lifted, and we were all on our way again as if nothing had happened.  Given how underprepared and ignorant we were (or at least I was), it was lucky no one crashed (it’s not the first time I’ve written about near-misses!).

Much more recently, I was reading a migraine-chatgroup on Facebook which was lamenting about brain-fog.  Most people tended to agree it was worst at the tail-end of the migraine; when the pain was subsiding but the brain had not yet returned to normal.  It was if, I thought, we were all still driving, just more slowly and deliberately; everything was stressful, anxious effort.  The only difference to the car-metaphor is that the fog was internal not external.

Because the fog is not visible to anyone else, there’s no real way for others to know what’s happening.  We don’t have hazard lights that we can switch on to announce what we’re going through, and remind those around us to slow down, have patience, accommodate the altered conditions.  It’s as if the Stephen-King-cloud is mysteriously (and oh so ominously) on the inside of our car alone.

Perhaps you’ve seen a car drive by that’s filled with smoke.  It doesn’t seem to happen much in Australia anymore (our smoking rates keep declining and I think it might be illegal to smoke while driving (especially when there’s kids in the car)).  Anyway, I can remember seeing a car full of teenagers shrouded in smoke decades ago.  I have no idea what they were smoking, but given they all looked pretty happy in their dusty-halo I could probably hazard a guess.

Pity that the fog that fills our bonnet rarely brings a smile to our faces.  We drive through the day as best we can, and if you’re anything like me on one of these days, the main thing that preoccupies your hazy-thoughts is your ultimate destination; home.

Migraine, like most chronic pain problems, is an invisible disease.  Many of us are so used to the pain, are so high-functioning, that others don’t notice we’re in the thick of it.  Perhaps we need to invent a way to show people where we’re at… a battery icon we can wear on our chest, (or a fuel gauge like the one I’ve written about before).  Imagine how convenient it would be; we wouldn’t have to rely on other people’s empathy or guessing.

If you or anyone you know is an invention-wizz, perhaps we could convince them to set aside whatever mad-scientist thing they’re up to, and ask them to invent us pain-people hazard lamps that blink when we’re lost in our brain-fog (just make sure the blinking doesn’t get in our eyes, because, you know, lights are a migraine trigger and all that!). 

Until then, I guess the best thing we can do is communicate with words.  In the same way I wrote about explaining to others about personal space boundaries, don’t assume others know where you’re at.  You might have to specifically tell people that part of your mind has gone ‘off-road’, and you’re metaphorically burning rubber and going nowhere, so please be patient.  It’s not demeaning, or demanding, it just makes common sense at a time when it’s not so common.

Take care and think clearly, Linda x 

PS – In one of those manifesting ‘trust the process’ moments, at about the same time I was putting the finishing touches on this post, I came across a global initiative called “Hidden Disability Sunflower” where you buy a pin, wristband or lanyard with the sunflower motif on it, and wear it as a means of letting the world know that you might be struggling and need a little bit more time and space to get about (it is basically a form of my proposed hazard-lights only much prettier). I am told by friends on LinkedIn that the project is quite well recognized in the UK (go you guys!) – but I haven’t seen them at all in Australia. There’s only one way to fix that – off to the shops for me!: HDS – Global (hdsunflower.com)

(Image source – The University of Reading, in England introduced the scheme on their campus in 2020… that makes me (and Australia) SO behind (oops!): UoR joins ‘invisible disabilities’ Sunflower scheme – UoR Student blog (reading.ac.uk))

Here are some stats from their initiative’s Migraine page (here):

PPS – based on the fact that 1 in 7 people get migraine, chances are you know someone who has migraine – so don’t forget to let them know about the little fledgling community we have going here… they’re always welcome.

PPPS – Let me know if you’ve seen the Sunflower logo in your country! xx


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40 responses to “Headlights For Brain-Fog”

  1. sedge808 Avatar

    ‘Where I live in Australia, we don’t get fog very often’

    same here. South Australia.

    Gavin.

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      Oh! I don’t know why, I assumed SA would be foggy… not as much as the ACT or VIC… but… there you go. I’ve only ever been to Adelaide once decades ago – all I remember (and I might be very wrong) is that it was very flat! Linda xx

      Liked by 1 person

      1. sedge808 Avatar

        I get excited when it happens. G

        Liked by 1 person

        1. The Mindful Migraine Blog Avatar

          🤣🥰

          Liked by 1 person

  2. joannerambling Avatar

    Don’t see fog around Newie much but it does happen, thankfully never while I was driving. I feel like I spent 4yrs walking around in a fog which has for the most part cleared now. I can remember way back when seeing a car of teenagers smoking with the windows up, what a stupid thing to do.

    Migraines are a hidden condition which is debilitating and one most people do not understand as they have never had a true migraine, just a bad headache they called a migraine.

    I have seen the sunflower pin being advertised and have thought about getting one for my sister Sue as BPD is also a hidden condition people do not understand.

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      I bought the sunflower pin as well – I think I’m more likely to wear that than the lanyard, because it’s more discrete. Looking forward to it arriving in in the mail so I can test it out. Glad your fog has lifted, and best wishes to your sister – BPD has a lot of stigma attached to it, so sending her lots of support! xx

      Like

  3. markbialczak Avatar

    We get fog frequently here in the Northeast U.S., Linda, and we say it’s like driving in pea soup. Not fun and could be dangerous, as your tale illustrates well.
    I like the sunflower pin, a lot. I’m all for allowing those who need a bit more of a wide berth all the space and time they require to navigate.
    You remind me for the first time in a long while that many decades ago, I had experience “helping” somebody close to me through her migraine bouts. She’d prefer me not to leave … lie still and quiet as can be … so at the end stage she could grab my hand and wordlessly just be there as she came back to normal.

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      😔your presence would have been a big comfort- during bad migraines even my heartbeat sounds too loud and an eye mask is too heavy, but the loneliness is often the worst thing after hours of pain. Small acts of kindness always make a big difference… and wow, does the world seem to need such kindness these days! Xx

      Like

      1. markbialczak Avatar

        The next time you are in that spot, Linda, you can think of an offered hand.

        Liked by 1 person

        1. The Mindful Migraine Blog Avatar

          OH! You made me a bit weepy – thank you!! xox

          Liked by 1 person

  4. Brenda Avatar

    Despite being in the UK, I hadn’t heard about the sunflower so need to check it out. Like your reader above, I also suffer from CFS and the migraines seem strongly connected with that. But brain fog is such a common feature with both. Having some visible, non-verbal way to communicate how I’m feeling would be great

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      On the advice of another reader, I’ve just purchased a tshirt that reads something to the effect of “brain fog alert” – it might be a fun way to remind people I’m struggling. I bought the sunflower lanyard, but I’m nervous about wearing it… it screams “look at me” in a way I’m a little uncomfortable with… but we’ll see… it really would be great, as you say, to alert people we need a bit of extra time.

      Liked by 1 person

      1. Brenda Avatar

        I also wonder if, during periods of brain fog I’d have the wherewithal to think about the sunflowers … but something would be useful going into class … but I’d need to be careful the students don’t try to take advantage. I guess pushing through when we’re struggling is something else we do, which can make things worse

        Liked by 1 person

        1. The Mindful Migraine Blog Avatar

          I hear you – I did wonder if I wore the lanyard then I might get extra help on public transport, but get charged double in a cafe! I know that’s not very kind, but the thought did cross my mind… pushing through is what we all do, and to be honest it’s all we can do sometimes, I guess it’s just important to take it easy when we can to give our body and brain time to rest and reset whenever possible. (Teaching would be hard with brain-fog though – you must be pretty seasoned and really know your stuff to make it work!) xox

          Liked by 1 person

          1. Brenda Avatar

            Yeah, I’ve been teaching for 21 years now but on the days it’s really bad I try to give them research tasks. It helps that I teach adults and it is a heavily theoretical area

            Liked by 1 person

            1. The Mindful Migraine Blog Avatar

              So impressed
              👏💜👏

              Liked by 1 person

  5. Destiny Avatar

    I agree with this, Linda …”whatever mad-scientist thing they’re up to, and ask them to invent us pain-people hazard lamps that blink when we’re lost in our brain-fog”

    though we’d have to omit the mad scientist part when requesting 🤭lol..

    have a great day 🤍💫

    Liked by 2 people

    1. The Mindful Migraine Blog Avatar

      Do you think? I sometimes think they wear the ‘mad scientist’ label with pride… but you’re probably right, better to be safe than rude! Xx

      Liked by 1 person

      1. Destiny Avatar

        with pride sounds good… put this way…I’d want to be a mad-scientist too…

        Liked by 2 people

        1. The Mindful Migraine Blog Avatar

          🤣🥰

          Liked by 1 person

  6. Edward Ortiz Avatar

    Great analogy, Linda. I remembered when we moved to Belgium that we had to install a rear fog light in the cars that we took there. It was a red light that we installed on the rear right side that we needed to turn on during dense fog. Instead of a big invention, maybe a shirt that says “Brain-Fog, don’t talk to me today” or something like that will do.

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      Oh gosh – great idea – I’m so doing that! Give me a couple of weeks to get it and I’ll be wearing that tshirt with pride!! I even found one with the headlight logo!!🤣

      Liked by 1 person

      1. Edward Ortiz Avatar

        You should post a picture if you do.

        Liked by 1 person

        1. The Mindful Migraine Blog Avatar

          It’s already ordered and on its way – stay tuned for a photo and full credit!! 🥳

          Liked by 1 person

          1. Edward Ortiz Avatar

            Awesome!!! 🤩

            Liked by 1 person

            1. The Mindful Migraine Blog Avatar

              🥰

              Liked by 1 person

  7. silverapplequeen Avatar

    I’ve never seen that sunflower.

    Migraine runs in my family. My mother got them; I get them; my older brother gets them. I’m not sure who else gets them.

    We have certain mental illnesses in our family. I am bipolar. We also have depressive illnesses, autism, eating disorders & anxiety disorders. How this may or may not tie in with migraine I do not know.

    In my own personal case, I am sure that a history of concussion (5+) has a bearing on my migraines.

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      The sunflower is apparently about 8 years old and I’ve never seen it either. The information about migraines being genetic seems pretty strong, whilst the information is more confusing about the relationship between migraines and other mental health issues (but the statistics appear to support there’s definite correlations), and I know there’s at least one other reader whose migraines started after a concussion a couple of years ago.

      Liked by 1 person

      1. silverapplequeen Avatar

        I had my first concussion at the age of 3 on Christmas Day ~ I fell down the cellar stairs. I’ve had concussions all through my life, because I was a very active kid. As an adult, I’ve had concussions because of taking beatings from violent men. My spine is disintegrating from these beatings. All these contribute to my migraines.

        Liked by 1 person

        1. The Mindful Migraine Blog Avatar

          I’m so sorry for the trauma you’ve been through 😔 it saddens me deeply that such bad people exist. I still only read positivity and generosity in the words of your blog which makes your resilience all the more astounding. It makes me feel humble too that my migraines are mostly related to stress and hormones, nothing like your legacy pain. Here’s hoping that the future holds the promise of such much deserved joy. Xoxoxox

          Liked by 1 person

          1. silverapplequeen Avatar

            “bad people exist” … remember, I live in the United States

            Liked by 1 person

            1. The Mindful Migraine Blog Avatar

              We have our fair share here too – the nightly news is overflowing with them – I’m just lucky enough to have only become entangled with a couple of them in my lifetime, and in both instances, I was lucky enough to notice the red flags (or have them pointed out to me) in time. xx

              Like

  8. Mike U. Avatar

    I’ve never seen the sunflower symbol in my area, but I’m extremely reclusive and never go out in public so it may be a thing that I just haven’t had the opportunity to notice. It’s a nice gesture, for sure, and I think it’s certainly a symbol deaf people could use as deafness is definitely an invisible disability. 🌻

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      Yeah, I’m very taken by the idea, but I’m also thinking that some people are reclusive or shy as you say. I’ve ordered mine, but I’m already a bit weak-kneed about the idea of wearing it… it draws attention to me when I’d often remain under the radar as it were. I think on a plane (which is where it started) makes sense, and maybe public transport, but not so much, say shopping… I’ll update you soon! Xx

      Liked by 1 person

  9.  Avatar
    Anonymous

    Half close your eyes so that your upper eyelid is sagging and your frown lines are at their peak and you’re sure to get someone say “are you having a bad day or do you feel unwell” “Can I help you”.

    Us Fibromyalgia and Chronic Fatigue Syndrome sufferers know exactly what you’re talking about with the Brain Fog term.

    Liked by 3 people

    1. The Mindful Migraine Blog Avatar

      I love the idea that people would offer assistance if you were friendy face, but I’m also (politely) a bit sceptical. I’ve been in situations where people seem to avoid those who look like they need help. Grab a can off a high shelf for a granny – sure, that’s easy and quick, but someone who’s struggling with their mobility; everyone seems to run away – maybe nervous they’ll make it worse?? Here’s hoping for a world with more empathy and less fog!! Xx

      Liked by 1 person

  10. Poetic Spirit Avatar

    Thanks for another great post. I always learn something new. Hope you’re feeling okay. Blessings.

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      Today’s a good day thank you! Happy to help 🥰

      Liked by 1 person

  11. Mary K. Doyle Avatar

    I see the similarity here. We had three days of storms and heavy air, which prompted a mild migraine. Your right in that no one else understands why we are a bit off.

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      I’m surprised when even my nearest and dearest seem bamboozled by my bamboozlement given how frequent it is! Sigh, we just have to keep 4WDriving it!! Xx

      Liked by 1 person

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