Whenever I’m having a difficult day, he goes out of his way to be silly and make me feel better.
I captured one of these moments last fall. On this particular day, I was feeling very scared about an upcoming doctor’s appointment. He threw on his silly hat, dropped to the ground to play with my feet, and started singing the Rocky Theme Song.
And it worked. I felt instantly better.
Humor is so important in a marriage. You never know what life is going to throw at you, and being able to laugh together, even during the serious moments, is a beautiful thing.
As difficult as it was being diagnosed with Multiple Sclerosis in 2016, it also Woke Me Up. It pushed me to take full ownership of my life, and to set long overdue limits and boundaries with everyone in my life. I now only allow genuine, supportive, and kind people in my inner circle. And the freedom I feel is tremendous.
My crisis started the first week of August in 2016. Within a few days’ time, I lost function in my left hand and forearm. Just like that. No warning. Boom. All the things I took for granted and did on a daily basis, I could no longer do. I couldn’t type, hold a plate, wash my hair, tie my shoes, open a jar, hold the steering wheel. It was terrifying. The medical appointments and MRIs that followed were equally terrifying. By the end of the month, I had a diagnosis. Multiple Sclerosis.
I spent the month of August in constant prayer, seeking God for strength and courage. I can honestly tell you that by the time I received the diagnosis, I accepted it gracefully. Was I extremely sad and scared? Absolutely. But I accepted the results because I knew by Faith that nothing just happens. That this was God’s will for my life.
Since that time, I have regained 100% function in my left hand and forearm. I still have the tingling sensation, but that is a minor inconvenience. The first gift I received from this crisis is that I no longer take my body for granted. Typing this post right now with both hands is such a blessing to me. Given there is no cure for MS and that it is a progressive disease, there is no telling what parts of my body will be affected and when.
Which brings me to the second gift of this crisis. If you do research on MS you quickly find out that it’s all a big mystery. They don’t know what causes it, they don’t know exactly why the medications help, and everyone experiences the disease differently. So basically, you are forced to accept the fact (that we humans try so hard to ignore) that life is unpredictable. You are forced to take life one day at a time, to pace yourself, to set priorities, and be adaptive. And this has brought great clarity and focus to my life.
The third gift of this crisis is that it strengthened my relationships with my husband, family, and friends. I found out on a much deeper level how much people loved me, valued me, and cared about me. I tend to be the strong one in a group, always taking care of others. It was very healing for me to be vulnerable and allow others to take care of me. I was surprised by people’s compassion and experienced incredibly sweet moments with my loved ones.
The last and most important gift of this crisis is that it has brought me closer to God. I know with 100% certainty that I could not live with Multiple Sclerosis without Him in my life. He gives me the strength, peace, joy, and courage I need to move forward in my life. And for that, I am eternally grateful. I leave you with a Bible verse that has been on my desk since the day of my diagnosis. “For I am the LORD your God who takes hold of your right hand and says to you, ‘Do not fear. I will help you.'” Isaiah 41:13