How Lupus Has Challenged My Desire for Control

I was one of those people who believed that thorough planning is needed for things to go as smoothly as possible. (Blame it on being an INTJ or having Monica Geller as favorite Friends’ character.)

At some point in time, I grew convinced that proper schemes, schedules and preparation would allow me to not only make the most out of every situation, but also to stay safe – yes, safe. That I could anticipate every little thing which could go wrong and equip myself to face it. That I would feel confident and at rest, enjoying peace of mind from knowing that everything was going to turn out fine because I was prepared.

And of course, it was just the opposite. I was perpetually anxious about not being aware enough, not getting enough done or not meeting deadlines which I imposed on myself.

Somehow, and fortunately, living with lupus is progressively challenging the control freak in me.

For a start, avoiding stress is an important part of preventing flares. I had to let go of useless responsibilities, learn to ask for help, and discover that things don’t need to go exactly as planned for them to turn out awesome.

Most importantly, however, was the understanding that I was dealing with a completely unpredictable disease – “a volcano,” as my rheumatologist sometimes call it.

No matter how hard I try to figure it out, a lot of things remain a mystery – hours of Googling would still yield results such as “It is assumed that…but no study proves…” or “More research need to be done to determine if…” or “…still remains unknown.”

On a day-to-day basis, I try to maintain a lifestyle which will minimize the frequency and severity of flares. But there’s a limit to what I can control and I can never know for sure how I’ll feel on a specific day. If one day my energy levels are at a peak, I might as well have to stay in bed the next. I make weekend plans knowing that I’ll possibly have to cancel them at the last minute.

In the long run, I don’t have faintest idea about how the disease is going to evolve. Will I develop complications? How am I going to be in six months, one year, five years? No clue.

All this was extremely disarming and I still often feel frustrated or vulnerable. On the bright side, however, it taught me to live for the moment in a way that no millennial wellness guru could ever have. The only thing I have for sure is now, and I’m learning to lean back and enjoy the freedom which comes from the absence of control.

This post originally appeared on With the Wolf.

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

Thinkstock photo via AntonioGuillem.

Find this story helpful? Share it with someone you care about.

Related to Lupus

text saying 'road to recovery' over a picture of a road

How and Why You Should Take Charge of Your Own Health

“Take charge of your own health!” “Be your own advocate!” These seem to be buzz phrases that we hear many people reiterate over and over again to people that are under a doctor’s care, have/had some type of illness or are trying to live a healthier lifestyle. However, nobody actually informs anyone of what this [...]
woman sitting in bed with dog

Why I Had a Photo Shoot With My Dogs After Doing Chemotherapy for Lupus

Recently, I did a photo shoot with an amazing photographer and close friend of mine. (I will include links to his pages at the end of this). I just finished my last round of chemo a couple of weeks ago for what will hopefully be a long time, if not forever (insert tentatively sarcastic chuckle). These [...]
Black and white image of a woman with curly hair, slight smile.

Why I'm Relieved to Have a Lupus Flare

This morning I woke up with the all-knowing feeling, “I’m going into a flare.” It’s the first one I’ve had since being in hospital over a month ago, and the last month has been pure bliss. I’ve been able to be a 24 year old and stay up late. I went out on weekends, still [...]
woman's arm with an IV in. she's holding a mug of coffee and studying for school

What 'Taking a Step Back' Taught Me About Accepting My Limitations

Over the past three months I’ve done a lot of soul searching and a lot of thinking, trying to grow personally. I have been learning to accept my limitations and to stop trying to fight the un-fightable. This all started around six months ago when I first made the application for Personal Independence Payment (PIP), [...]