For most of my life, the same people were around me. I’m sure we had our awkward moments, but my friends had grown comfortable with my disabilities. Past the third grade, I don’t remember feeling as if I needed to “train” my friends on how to handle my high-risk limitations.
If my friends had questions about my disabilities, they either didn’t ask them, or they learned to watch me closely and found the answer themselves. My world was simple. My friend group was small, but everyone had my back and I had theirs. Any chronic issues of my life were talked about as if they were everyday occurrences and common knowledge.
Over time, I forgot I was disabled. But then I returned to Indiana to attend college.
All the sudden, my body-guard best friends were nowhere to be found. I was the new kid on the block, and I was obviously an oddity that needed observing. I quickly discovered my disabilities were still scary to some people, and down-right annoying to others. My confidence took a hit every time I had to apologize for my twitching limbs, my awkward stutter, or my random seizures.
It felt even worse every time I had to explain my limp, my crooked arm, or the reason I eat food with my right hand squeezed between my legs at all times.
I swallowed my pride and pushed forward, though. My new circle of friends learned to chuckle at my quirks, accept my limitations, and they realized asking for help didn’t mean I was weak. For the first time in two decades, I had to learn how to teach my friends.
Learning how to teach Peter, first as a boyfriend, and then as my husband, was a totally different experience. He had a right to know what was actually happening to my body, but all I wanted to teach him was how to cope with the awkwardness of my existence. I felt like I had something to prove.
Every time I attempted to prove to Peter that loving me was a totally normal and romantic adventure, I failed miserably. Most times, my attempts to prove my independence and strength left us both hurt, scared, and confused. For a time, I didn’t really care about the price of my short-sighted actions.
My antics were based on my fear of losing Peter. I was confident that if he realized how broken the cage of my body was, he’d walk away from me entirely because I was too high maintenance. I had to learn to trust Peter, and I had to learn to accept that God could equip Peter to handle my disabilities better than I ever could. We both learned—through trial and error—that our marriage needed authentic transparency and a willingness to talk through anything.
Training my friends how to handle my disabilities had been easy. I helped them cope with the differences because I love them. But with my husband, I had to let him help me bear the load because he loved me. Supporting me and defending me are two things he is biblically called to do as my husband.
I had to learn how to trust Peter’s heart and countenance with the Lord. When we confront yet another medical hurdle, I’m often unable to be exactly what Peter needs in a wife. It’s during those seasons, as a wife, I run to my Jesus and shout at the top of my lungs, “In my weakness you are strong, Jesus. You have to be enough.”
Our marriage is beautifully lacking in quite a few ways. But when my physical limitations force me to fall short for Peter, I’m forced to look for Jesus. And in much the same way, when Peter can’t fix, understand, or help bear my turmoil, he is forced to realize in a much deeper way that Christ is my savior, not him. We’re both learning to remember that although we may still be learning what coping with disabilities is like, Christ is all-knowing and never had to be trained in the first place.
(Over the next several months, to find the other blogs in this series, type marriage with disabilities in the search bar.)