Family · Health · Perspective

Living Heavy

Pandemic. Do I dare even say the word? I’ll just refer to it as “the big P.” It has us all fatigued. People are living heavy. We are edgy and impatient. My daughter calls it “harsh.” I believe it’s directly correlated to the overall environment the last couple of years.

In retrospect, WE were living with force. I was stressed trying to balance all the moving parts and keep us healthy. Constantly questioning myself if this was a good idea? Are we going to get sick? If we do, how sick will we get? What will it disrupt? School? Work? Let’s balance the kids’ need for socialization (school has been IN PERSON the whole time) with making health-based decisions. Make sure you are washing your hands! Who was sick today at school? It was exhausting. Just keep moving. For two years we lived like this.

Christmas Day all the questions were answered. I got sick with what seemed like a bad intestinal flu and fever early in the morning. I don’t remember Christmas at all. My husband wanted to wait to open gifts until I got better, but I refused to make the kids postpone Christmas morning. Scoot forward to day 3 of being sick and I took a home test. Positive, very quickly, I might add. Rona had finally hit our house. Day 5 (fever free!) I emerged from my room (without a sense of smell and modified taste) to my 11yr old son not feeling well. He ran a fever for 12 hours, headache, and intestinal issues. Two days later, I had a cranky 9year old with a stomach ache and headache. The final domino to fall was my husband. That night he developed a fever. He was sick for 36hours (intestinal) and thought everything was extremely salty. Weird.

We live in a rural area, so by the end of our self-imposed quarantine we loaded the vehicle and went for a country cruise. Interacting with no one, it was just a nice dirt road drive to get out of the house. Then it was over. Done. We’d missed Christmas with my family, a basketball tournament, work, and a gathering with friends. We put together puzzles, made Chex Mix, did crafts, played games, and watched Christmas movies – all together. Everyone recovered without medical intervention. No one experienced the respiratory symptoms. What a bizarre experience!

I have mixed emotions that I’ve discussed with my therapist. Part of me feels guilty that we had absolutely no complications. Even with my MS, I had no issues other than my illness lasting longer than everyone else in the family. It’s been drilled into us that if we get C19, we will die. If we get C19 and you aren’t vaccinated, or your immune system did not mount the proper response (hello autoimmune), you will die. Even if you did get vaccinated, you might have complications and die. Many people have. In no way am I downplaying that fact. It IS a fact. It’s a terrible, sad fact and I have grief and empathy for those who battled unsuccessfully. And yet, we didn’t. Survivor’s guilt.

On the other hand, I feel IMMENSE relief. After two years of somehow managing to avoid it, we’ve made it thru. We can live a notch lighter. I know we aren’t alone in this. I read an online article out of a major US city that voiced these exact feelings, both the guilt and the relief, from a handful of people the author interviewed.

A good friend of mine described the same situation after her family went down with C19 in January. We felt shame for being sick with it, followed by relief and guilt when we recovered. Neither her family nor mine was broadcasting on social that we were positive. We quietly let our immune systems battle it out in the privacy of our homes and told only people who had to know- family and those we had been around in the days prior. After recovery, we told our closest friends. That’s it. Why the stigma? We’ve all been living in the big P for 2+ years. Now, 2.5 months later, I feel comfortable writing about our experience and the reflections on it. I’m tired of living heavy. This is a step towards living lighter.

Life in QT over Christmas.
Fitness · Health · Perspective


Swim. Run. Bike.

A couple of weeks ago, I completed my second indoor sprint triathlon.


300m lap swim- this is actually only 6 down and backs in our local Wellness Center’s pool. 78 laps done in the previous weeks before I completely fried my hair with the chlorine and purchased a swim cap. Pink swim goggles and my navy one-piece- I felt pretty official! I managed to cut 1.5 minutes off my previous race time in swimming.

2mile run- Running is my jam. I like to get into a rhythm and just go for miles. However… sprinting is NOT my jam. Nerve pain and numbness in my leg plagued me most of the winter. My mileage was dialed way back. I didn’t expect the time to be good. Vomit was close to erupting, but I beat my previous two mile triathlon sprint by about 20seconds.

12mile bike- After the fall sprint tri, the organizer decided to add 4 miles to the challenge. My spinning seat wasn’t set correctly… my fault. Shredded legs and a little rub discomfort. About 2:10/mile.

Overall, I took 3rd female. I thought I would feel proud of my physical accomplishment.

Upon reflection, all I felt was humbled. Two days before this, I laid in the tube for two and a half hours. My annual MRI: brain and thoracic spine, with and without contrast- a yearly peek into my neurological system.

All stable. Nothing new. I’d have loved to hear that my lesions miraculously healed themselves. Same white dots in the same spots.

Randomly, I’ll have weird nerve and muscle symptoms. For years, I thought everybody did. Apparently not. MS does odd things.

Have you ever considered how fortunate you are to have working legs, fingers that feel, and a spine that doesn’t “buzz?” This isn’t for sympathy. These truly were not situations that I’d considered prior to about four years ago.

Humbled to be able to swim. Amazed at running. Grateful for biking.