I’m lying on the couch, contemplating how often we take our health for granted.
Sometimes I mourn the girl I was before this, before I found out Lyme was the reason I’m not myself, why I’ve been constantly exhausted and experiencing weird symptoms for the past three years.
It’s evening. I am one with the couch, my legs feeling like stones, heavy and detached from my body. I’m thirsty, but too tired to walk to the kitchen to get a glass of water.
The only thing that motivates me is the “poison” I need to take in five minutes: the antibiotics that have filled my belly twice a day for the last four months, aimed at fighting this “sentence.” So I start moving to the edge of the couch, telling myself, “You can do it.” And I do. I’m proud of myself that I also managed to brush my teeth to get ready for bed, as I can feel my energy “left the building” an hour ago, and I’m literally running on fumes.
Someone once told me Lyme is a marathon, the path to recovery is long and painful. Now I get it: slow progress in symptoms disappearing despite taking antibiotics for the last four months, not knowing how tomorrow will be (good or bad), symptoms reappearing, and feeling like you’re starting from scratch every time you change something in the treatment.
Sometimes I wonder if all this will go away, if I will be the fortunate one to say I beat it, or the less fortunate who will struggle with this until they are “done and dusted.”
I guess I’ll see. I’m curious how next month’s travel of 600 km to see the Lyme specialist will go. Will she say I need to take the “poison” for one more month, or will the symptoms go away? I guess we’ll see. In the meantime, I will enjoy the sun, the sausage dog in my lap, and maybe a good sauna break this weekend.
