Closeup of a hand holding a flight ticket tucked inside a passport. Blurry background of an airport scene.

Balance Awareness Week 2023: Airport Spins

Image by Joshua Woroniecki from Pixabay

Making my way through the queue barriers, zig-zagging through the empty pathway, I feel like a mouse in some cruel maze experiment; dizzy and weary

I reach the queue at the security screening area and start to feel disorientated and lightheaded. It’s the height of the summer and travellers are packed into a small area, taking liquids and electronics out of their bags, grabbing extra trays, and walking through the scanners. The airport workers are shouting instructions: “Take out all your liquids, remove your belts, move forward.” I remove my laptop from my bag and place my phone next to it in the tray. I walk through the scanner, feeling slightly queasy. 

The artificial lighting causes pain behind my eyes. While standing by the conveyor belt, I notice my bag has been selected to be searched, while my laptop and phone pass through the scanners in their tray. I collect my belongings from the tray and go to stand near a wall where I can see the airport worker who is holding up people’s bags to be checked. My partner comes to stand next to me. 

I begin to feel hot. My surroundings are spinning. I cling to my laptop. Deep breaths. I focus on looking forward. My ears are ringing and the feeling of pressure in my head is building. 

The airport security officer checks a traveller’s bag, removing the forgotten liquids and putting them in a tray. Next, one of the traveler’s friends is called over and his bag is also checked. They’re part of a small group of guys travelling together, who are laughing and chatting. 

Voices are loud and distorted. People are walking past in a constant stream, leaving the area. I’m unsteady and overwhelmed. I lean against the wall, which offers support. Deep breaths. Time slows down. Ten minutes feel like multiple hours, as I wait to be called. 

Finally, I see the officer holding up my bag and I make my way to a metal table. I struggle to hear her instructions and tell her I am hard of hearing. She speaks across the table to me in a clear voice and I proceed to open each section of my bag for her to check. We find the culprit—a small bottle of hand sanitizer tucked away in the front pocket. I’m annoyed at myself. I could have spared myself this unnecessary overwhelm if I had just checked more carefully. I focus on remaining composed, smiling as the airport worker hands me my bag. 

I make my way out of the security area, through a corridor towards the Departures area. My knees buckle and I crouch down. The buzzing in my ears reaches a crescendo. I’m hot and the lights are unbearably bright. Disorientated. My partner helps me towards a chair and I sit down. Hunched over, staring at the floor. Exhausted. Embarrassed. Frustrated.

I am a seasoned traveller, living with Ménières disease and vestibular migraines. I am determined not to let my vestibular conditions stop me from exploring the world and visiting friends and family. But, it can be hard. Triggers such as visually busy environments and artificial lighting cause me to feel unbalanced and have heightened sensitivity to visual and audio stimuli. I have moments of feeling dizzy and disorientated, my tinnitus increases, my head aches with a feeling of pressure, and sometimes I feel nauseated. 

I’m writing this for anyone who finds busy and bright environments challenging: Know you are not alone. This recount is also for loved ones of those with vestibular disorders to hopefully stumble across one day. I hope my story will help them understand how difficult busy environments such as airports can be for people with vestibular disorders.

Do you also have a vestibular disorder? What environments do you find challenging?  Please share your experiences in the comments.

4 comments

  1. Good morning Carly! My name is Carolyn, I live in the pacific north west in Washington State in the U.S. and I too have been diagnosed with Ménière’s disease and Vestibular Migraines! I’ve had it since late 2019 and it was sudden onset after two sinus infections. I have had every test imaginable! I’ve been to vision therapy, balance rehab, and I’m going to do vestibular rehab again in November; however not looking forward to it!
    I wear concert ear plugs in loud places- I can’t handle the noise! I can’t go to shopping malls- or any other place that is “visually busy” I start to spin, get more off balance, lose spatial orientation- well, you know the progression!
    Thank you for writing your blog! I just came upon it in my search for vestibular treatment!
    I push through most days until I’m forced to stop and not move at all!
    I’ve cut down on work to 3 days a week; however electronics trigger the vestibular migraines! Artificial lights trigger, walking through the airports, I rarely fly any more. Restaurants can be triggering which I used to love going out to eat. Barometric pressure changes are big for triggers!
    Anyway, the louder and visually busy any environment is- seems to impact my vestibular system!

    Thank you again for sharing your story! It’s good to know I’m not alone and someone else gets it!

    Many blessings and peace be with you~
    Carolyn

    Liked by 1 person

    1. Hello Carolyn,
      Great to connect! Wow, your triggers and symptoms sound just like mine, though this all started for me after a sudden hearing loss. I also had vestibular rehabilitation, but quite a few years ago. I think it helped a bit. I have found that it is important for me to keep challenging myself everyday – going outside and moving. I also try to eat healthy, I do yoga, and walk a lot. Lack of sleep, travel, and weather changes are big triggers for me. I hate shopping malls too! – too much articficial light, people moving around me, and all the products on display! I absolutely understand your experiences of vestibular disorders and agree – it’s good to know we are not alone in this.
      I recently started having Botox injections to help with the vestibular migraine. I have juts had my third dose, which was an increased dose (they are every 3 months) and am still monitoring my symptoms to determine whether the Botox is helping. I will be writing a blog in January after my 4th appointment with the verdict 🙂 So far, my “bad” days have definitely reduced, though I do still have frequent flare-ups.
      Wishing you all the best with managing your symptoms.
      Carly

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  2. Thank you Carly! Yes I have a hearing loss in both ears, it’s not yet to the point of hearing aids-perhaps I’m in denial about needing one more thing because I notice I can’t hear certain sounds and I ask people to repeat things frequently! I’m looking forward to reading about your verdict on Botox as my neurologist said that is the next step after Ajovy which helps dampen the symptoms, but I am still chronically off balance with a feeling of dizziness like yourself! I don’t let it hold me back either I try to enjoy all that I can:-)

    Wishing you a wonderful holiday season!
    Best,
    Carolyn

    Liked by 1 person

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