I haven’t written in a while, mostly because life surprised me with something I hadn’t seen in months: energy. Real, functioning, 100%-battery-kind-of energy. And when you live with chronic Lyme, that’s basically winning the lottery. So for the last four weeks, I’ve been busy enjoying it to the fullest, like a kid who found the hidden candy drawer and refuses to tell anyone.
Now here I am, back in the passenger seat of my monthly pilgrimage to the Lyme specialist, the holy temple of antibiotics, blood tests, and “So… how are we feeling today?”.
And honestly? I really hope this is the last one. I feel good. OK, not “perfectly-oiled-machine” good, more like “the washing machine makes a weird sound sometimes but still works” kind of good. But that’s absolutely fine.
Obviously, my body decided to spice things up with a new symptom (because why not keep the plot interesting?): red, itchy hands in the morning. Cute. Annoying. Manageable. We deal.
But holy hell, the energy. It’s back. In full force.
And I feel invincible.
And it’s absolutely fucking awesome.
It’s strange to think that it’s been a year since I first heard the words chronic Lyme. I remember that moment so clearly, relief because I finally knew why I felt like a malfunctioning 90-year-old trapped in a 40-something body… and fear because I had no idea what came next. So my brain, being the loyal overthinking factory it is, went into full detective mode. Google tabs everywhere. Supplements everywhere. Hope and panic in equal doses.
But somehow, one step at a time, paths unfolded.
And now, one year later, I’m… different.
Wiser. Tougher. More resilient.
My mind and body have been to war together. I’ve learned so much about myself, especially how to say no without feeling guilty. And damn, that felt good. Like unlocking a cheat code in life.
So here I am again, in the car, staring out the window, mentally preparing for the doctor’s office. Except this time, my list of concerns has exactly one item:
“Can I stop antibiotics, please?”
That’s it. No dramatic monologue. No existential crisis. Just a quiet, hopeful question.
And whatever happens next, whether I stop today or in three weeks, I know the direction I’m going. I’ll keep supporting my body, but this time I’ll let the plants take over the battlefield. A softer army. A greener one. One that taste better than tinidazole, for sure.
Here’s to energy returning, to surviving the toughest year of my life, and to hoping this is the beginning of life after treatment, where the only thing I fight is the temptation to say “yes” to everything.
