Today’s a difficult day for me. Air travel. It’s nothing new, in fact as a nomad I travel constantly from state to state depending on what seasonal job openings there are. With epilepsy it’s not impossible to get a driver’s license, but I’d say it’s more on the rare side if someone with epilepsy drives. Having photosensitive epilepsy (affected by flashing lights) is rarer than people think if they’ve never met someone with epilepsy. Only around 5% of people with epilepsy are photosensitive. If you’re interested I explain my epilepsy in more depth here: Formerly Known As Petit Mal: My Epilepsy
“Ambulances for me, are like irony on wheels.” from BBC Three Video-Things Not To Say To Someone With Epilepsy
When I’m traveling there’s a few guidelines I like to follow to make traveling with epilepsy less stressful and more enjoyable. Note that this is the system that works for me, everyone’s epilepsy differs, and their needs may vary.
Plan Accordingly: The best time to purchase a flight is around fifty days out from the departure date. I recommend choosing an aisle seat if possible. Giving you plenty of time to organize things you may need such as extra medications for longer trips.
Sleep Well: A lot of flights, especially if you’re on a budget like me, may be more financially friendly if they’re early departures or red eye flights. No shame in being budget smart but be sure to get an adequate amount of sleep the night before if you’re not a fan of sleeping on planes. (Around 8-10 hours.)
Come Prepared: While traveling I usually have one checked bag and my backpack as a carry on. In my backpack, alongside my laptop and my current novel obsession, I have my emergency medication and an extra pair of clothes folded neatly inside a plastic grocery bag.
Medical ID Bracelet or Necklace: Having some sort of medical ID with your name, home address, primary care physician or emergency contact number could benefit you in case of an emergency.
Communicate: Admittedly, the first time I tried to converse with people sitting next to me I was quite embarrassed. However, more times than not we end up having an intelligent conversation on epilepsy and they speak about their friend that has epilepsy or a family member. Communicate to them that there’s a possibility of you having a seizure and what they can do to help. We’re all human.
Out of the dozens of flights I’ve taken, I’ve had two seizures at the airport before boarding and none while airborne. (Knocks violently on every piece of wood. Ha-ha.) By becoming more comfortable and actively speaking about my epilepsy to others, I believe that air travel has become less stressful overall. Taking the time to note what I need to be safe and relaxed while traveling instead of worrying what others might think was the most difficult, but most important note I remind myself every time I fly.
I hope this finds you well and that you don’t let your epilepsy deter your traveling desires. If there’s any travel tips I missed or some that you’d like to add, feel free to comment below!
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