This is my husband Terry dancing up the sidewalk to retrieve our newly delivered beach chairs after returning home from work. We finally have steady warm weather here in Green Bay, Wisconsin. Photo is a still image courtesy of our Ring Video Doorbell.
This is one of my favorite photos of my parents. They were visiting me at my home in San Diego, California in 1998. I was working on my Ph.D. and hadn’t yet decided which state I would seek licensure as a Psychologist.
After completing my postdoctoral residency in 2001, I decided to move back to the Midwest. I proceeded to get my Psychologist License in Wisconsin.
My parents were still able to enjoy the San Diego house during the winter months after my dad retired full-time in 2002. They were very happy to get a break from Northern Illinois winters.
In this photo, they are sitting on my back patio, which could not look more different than my current back patio here in Green Bay, Wisconsin.
I Knew Something Was Wrong
I’ve had a love for swimming since I was 4 years old. I learned how to swim in a pool in Pompano Beach, FL during one of our annual Florida family vacations. I later enjoyed using this pool at Forest Hills Country Club in Rockford, IL where my parents have been members since 1980. I was on the FHCC swim team and basically lived there during the summers in middle school, high school, and college. (Photo courtesy of Forest Hills Country Club)
Fast forward 20+ years to July 2016, and I am using the pool at the Princeton Gym in Madison, WI. I was just starting to get back to swimming laps, and I noticed that my left arm felt heavy and numb. I told my husband that something was wrong, and that was the beginning of a very scary time for us. My MS diagnosis came on August 26, 2016.
It is common for people that receive a life-altering diagnosis to go through a grieving process. It takes time to accept your new “normal” and to heal from the medical trauma that you endured. I am very thankful that I’ve had the resources, support, and education I need to adapt to my life with Multiple Sclerosis. I realize that not everyone has that, and I don’t take it for granted.
My husband Terry Clark just had his best sales year ever. He absolutely loves his job which draws on his natural talents and abilities. At 55 years old, he has definitely hit his stride. We are forever grateful to God for giving him this work opportunity 7 years ago, which brought him to Madison, WI where I was living at the time. We moved to Green Bay, WI 4 years ago so that he could help build an office and service area here.
I can’t lie. When the temperature in Green Bay, Wisconsin drops to -6° F (-21° F with wind chill), I miss the gorgeous San Diego weather. I lived there 8 years for graduate school and a postdoctoral residency. In those days, socks, coats, hats, and umbrellas were of no use to me.
My husband just left for work and said to me, “Stay in and stay warm.” Yeah, that won’t be a problem. I already have the fireplace going.
The Gift of Crisis
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
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