How Travel Planning Changes With Lupus


Traveling is one of my greatest passions. From the very first moment I set foot overseas, I was hooked. I love the culture shock and being thrust into a world that’s completely unlike anything I’ve ever known. But traveling with a chronic illness is potentially dangerous on so many different levels, and never again will it be as easy as it once was when I was healthy.

There are so many “what ifs” involved in traveling with an illness like lupus, especially for the newly diagnosed like me. I don’t know what to expect on a daily basis, let alone when I’m completely out of my comfort zone in a foreign country with no safety nets whatsoever.

 

What if something goes horribly wrong while I’m traveling? What if my health starts to rapidly decline without warning? What if I present with symptoms I’ve never seen before?

I know traveling is risky, but whether I do it now or later in my life doesn’t matter. The risk will remain. The difference between traveling now or in 20 years is that I’m likely to have a much better understanding of my illness later in life. But that’s all that I know for certain.

I don’t know how fatigue will affect me in the future or if traveling will even be possible due to other complications. The time is now while I know I can.

The path to boarding the plane was arduous. Packing for an extended period of time is tricky in the best of times, but throw in a chronic illness and it’s headache-worthy. My greatest worry was medication. Though my condition is constantly improving, the medications I take daily — especially the immunosuppressants — are the only thing standing between me and a serious downward spiral in my health.

Knowing I was going for a month, it wasn’t a matter of just making sure I had sufficient medication for a month, I also had to consider the worst-case scenarios. What if I lost my luggage? Would it be enough to take it all in my carry-on luggage? But what if I lost my carry-on as well?

Ultimately, I couldn’t risk tempting fate. I’ve packed two months worth of medication so that unless I somehow manage to lose my luggage and have my carry-on stolen, I will always have at least a month’s supply on me. At the end of the day, I have to take the safest option as it’s not like choosing to leave a pair of shoes at home. I’m potentially playing with my health, and it’s just not worth leaving it to chance.

I have to admit sitting on the plane that part of me is terrified. This is not going to be like any other trip overseas, and I already knew it would be so much more difficult. I have to take my energy levels and fatigue into account, making sure to always listen to my body. I need to protect myself from the sun and make sure to take care of my photosensitive skin. And don’t even get me started on how stressed I am about trying to maintain my low-sodium diet through Europe!

two women taking a photo in front of the roman forum

But at the same time, after all I’ve been through in the last year, I know all of the hardship will mean this trip will be that much better — and that much more memorable. Although I know many people are worried about me, I needed this trip, and nothing was going to stop me from going. In the last 12 months, I faced personal hell with my health and I deserve the chance to chase a passion, the chance to have something good for the first time in a while.

I can’t ever escape lupus; it’ll follow me everywhere I go and make certain my life is never easy. But that won’t stop me. If it’s wrong to take risks, then I’ll live my entire life incorrectly because difficult doesn’t mean impossible. If there’s ever a chance, I want to take it — despite lupus!

This post originally appeared in Kristiana Page’s column “The Girl Who Cried Wolf” on Lupus News Today.

We want to hear your story. Become a Mighty contributor here.

TOPICS
JOIN THE CONVERSATION

Related to Lupus

illustration of a woman with colors splashed across her face

How Refusing to Define Myself by My Illness Causes Me to Forget My Limitations

I was a lot of things before lupus, and my diagnosis hasn’t changed. Of course, it is undeniable that my life has been altered by chronic illness, but not nearly as much as many might assume. When I think about what I’m capable of, my mind doesn’t go straight to how lupus may limit me. I tend to [...]
A woman lying awake at night, with a clock in the foreground.

What It's Like to Have Sleepless Nights Because of Lupus

Part of living with lupus is knowing that your body lives outside of the norm. It means accepting that, for the most part, you have no predictable sleeping pattern. And, if you should be lucky enough to regulate one, it’s pretty messed up. Living with lupus means you don’t live on the same timeline as [...]
illustration of a woman with light hair

Why I’ll Be Unapologetically Vocal About My Life With Lupus

Some might be ashamed of their status as someone with chronic illness; however, I’m not. I wouldn’t say I’m proud of it, but it’s also not something I’ll ever work to hide from the world. In fact, I’ll endeavor to share it as much as possible. Worldwide, millions of people are diagnosed with lupus, yet there’s [...]
A tired female runner, taking a break from her run with her hands on her knees.

Why I Tell People Chronic Illness Is 'a Marathon, Not a Sprint'

“It’s a marathon, not a sprint.” It’s something I tell people all the time about chronic illness. I know this in my heart, I know this in my head and on the good days I know this and understand. On the bad days, I’m tired of the fight, I’m exhausted from the non-stop battles, I’m [...]