I saw it coming, though ever so subtly. I would be sitting at a table talking with a friend, and the whole room would shift as if balancing on a delicate axis. I’d sip water and concentrate hard—on anything—until it would pass, only to have it wash over me again like a line of unending waves in the ocean. It quickly accelerated from occasional to everyday. I’d find myself sitting in a coffee shop working on a project, and having to brace the table before me to steady myself, although I wasn’t actually falling—yet. And so, on the day when it finally gave way, I was not too surprised to find myself collapsed on the couch for the whole of an afternoon.
It is difficult to remember that this used to be my regular existence.
Over a decade ago when I sat in that sterile room, my parents in those cheap chairs next to the exam table where I sat fidgeting; the doctor spoke it, “Yes, she does have Addison’s Disease”, and I wonder if we knew at all what it meant.
Back on that day, we wondered whether it would mean that I may not be able to have those three babies I kiss goodnight every evening now. Or that I should probably never try anything like running that half marathon I completed a couple of years ago, our third boy nestled safe in my womb as I crossed the finish line. I don’t think we knew back on that day, in that little room, when words of prescriptions and doses and tests were exchanged, really what kind of life I could expect to live. If I could ever chase big dreams like writing books or starting businesses or raising babies. We had no idea what to expect, aside from limitations.
Sometimes, on the hinge of words spoken or a diagnosis given or our own doubts crowding—we become a little afraid to dream. Because who wants to dream a dream that their limitations—be them physical, emotional, or other wise—will never allow them to chase after?
In that first handful of years following my diagnosis, my parents fought hard to dissect this disease, and learn every little detail of how it might be affecting my body. And they fought even harder to encourage me to never stop dreaming. And then, five years after we sat in that sterile room, they handed over the position of Chief Encouragers to my husband, as we stood on that altar and exchanged vows. And as he took my hand, he eagerly took on that responsibility to never let me give up on my dreams.
And he’s kept that vow.
And so, on weeks like these, when seasonal colds and stressful weeks culminate in my disease reminding me—hey, I’m still around—I’m caught a bit off guard.
We have a way of forgetting about our limitations. Somehow we become comfortable with them. We tame them. We create a system, balance the weights, and set up safe guards. It’s what my husband and I have been fighting for over the past years, as we’ve learned how to live a life abundantly—with a chronic illness. It’s a good thing. But then, when we finally become comfortable and well adjusted—we round a corner to find those inhibitions staring us in the face—the floor falls out from beneath us.
Whether they be physical, emotional, mental, or spiritual—whatever these limitations be, they have a way of reminding us that we are but clay and dirt and finite. We are limited. And it hurts, to want such big and beautiful and wondrous things for our lives, but to feel terribly hindered by things outside of our control. It hurt this week, in the midst of big dreams and plans and deadlines, to lay on that couch unable to even make dinner for my family.
And yet, I am discovering that my limitations are an invite.
This week, they invited me to lay and read that book I’ve been too busy to pick up. They invited me to watch my boys as they ran circles around the house in boy-made Superhero capes, exclaiming “It’s my pleasure!!” Every time I would ask them to grab my notebook or my blood pressure cuff.
My limits were my invite to not care about the dirty socks and half-completed art projects scattered across the floor, but instead to hold my toddler boy as he waited for me to fix his Lego truck. My limits were my invite to remember that I am, indeed, limited—and that’s ok. In fact, once in a while, I need to remember those limits. Because they have this stunning way of springing up within me a longing for that which is above and beyond and bigger than me and my limits. They make me ache for my Creator, who made me wonderfully, and calls me Very Good. The One who is my strength in weakness, my ever-present help. These physical limitations that drive me to that couch or my bed—they also drive me to my knees in prayer. And call me crazy, but it makes me a little bit fond of these hindrances.
Our limits have a thing or two to teach us about ourselves, our loved ones, and the pace of life. Sometimes they are our invite to rest, when we’ve been to stubborn to give ourselves a break. They invite us to ask for help, to accept grace, to stop. Refocus. Refresh. Restart. and Remember the One who gave us life, calls us to great things, and gives us everything we need—right in the midst of our limitations—to pursue those great things.
Back on that day when the doctor handed me a diagnosis I couldn’t, at fourteen years old, begin to understand the intricacies of, I couldn’t have anticipated the gifts hidden within. Limitations are funny like that, don’t you think? A blessing in disguise, if we choose to see and treat them as such. What is that limitation staring you in the face today? They stand there, intimidating and threatening and discouraging—and inviting. Take the invite today. The one that calls you to your knees, to rest, and to embrace a life that says that we are not enough—and that’s ok.