Catching the Heart Up with the Body

When I was 24, first diagnosed with Lyme, suddenly living in suburbia with my parents and swallowing down more pills each day than I had taken my entire life, I couldn’t let myself fully know how sick I was. If I did, I wouldn’t have been able to keep putting one foot in front of the other. So I told myself, daily, that I would be back to life on my terms in a few months, six at the most.

Nine months later, I had a P.I.C.C. line in and was on I.V. antibiotics. I ate breakfast and dinner with my drip going. Still, I told myself that I would be able to pick up where I had left off from my life in NYC. Ok, I had told myself a year in to living back in suburbia, I’ll be back to life in six more months, in another year, tops.

But it takes time to get as sick as I did and it would take another decade to get fully better. Over the years, I spent most of my time and money and energy trying to get better. Over the years, I slowly stripped away symptoms as I unraveled the layers of illnesses. I lived a half-life out of necessity. My health, or my approximation of it, was in delicate balance. If I pushed too hard in any aspect of my life, my health would collapse. I felt like a house of cards and the slightest thing outside of my routine—a missed meal, a forgotten hat and scarf on a cold day, a too late night, relationship strife—would knock me down.

I spent a lot of time in bed, waiting. I held myself back from living as hard as I wanted to, telling myself that once I was healthy, I’d have everything.

During that decade of living small and contained, I told myself that I would have everything once I had my health. I told myself that it wouldn’t matter how little I had done over the years; once I had my health I could approach everything in life with the vigor I wanted to. Now I am where I once only dreamed of being and feeling. And though life without illness is so much better and easier and thought I am doing everything that I want to be doing, I am surprised to find that the underlying emotions for me are a dull sadness and defeat. It is because, only now, in being healthy, do I understand just how very sick I was and can I know just how much I missed out on.

I am surprised to find that I am not just living in a state of elated joy, which is what I thought that I’d be doing once I got better. I’d have everything, remember? Of course I have to work through the dull sadness of loss. I fill the time that used to be filled with taking care of myself with meditation and long walks and fostering friendships. I am taking it easy and gently this winter and making sure to cook up soups and stews and ciders that are rich in color, scent and taste.

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Gratitude

There was a time that, when I thought of myself, the image that came to mind was of an old clay pot, dropped and shattered and badly put back together again. At that time, I was in so much pain, I hobbled when I walked and was so tired that I became anxious at the thought of leaving my apartment. I was 22.

These days, I write posts on healing, on compassion for the body—your body and how to train when dealing with a chronic illness. As I write, I always return to the time that I was sick for understanding, for a way in, for compassion on what my clients and readers are dealing with in their bodies.

Yesterday, I wrote on pain and when I did, I remembered when the pain and the fatigue were hardly indecipherable from each other. I was so tired that it hurt to be awake; I was in so much pain that it exhausted me. I remembered, as I wrote, how weak I used to be, as if a strong breeze could take me down. As I wrote, I recognized how strong and resilient I’ve become and how the sick person I used to be is no longer true.

When I think of myself now, I have an image of a giant trampoline, of its ability to bend deeply to the blows of people landing and regaining its shape so rapidly that it throws them in the air again.

I remember how it used to be, when there was no end in sight of Lyme Disease for me, just an endless slog of days marred by illness. The end of Lyme finally came but it seems that I was so busy living my life that I hardly noticed it until it had passed.

Hyperbaric O2 Treatment Number One

After the session, my eyes were open wider than they have ever been, I could not find a trace of fatigue anywhere in my body and my mind was awake and fresh and bright in the way that I am looking for but never find when I drink coffee.

I am pissed! Is this what healthy people feel like? Or could feel like if they took care of themselves? In this moment of brilliant mental clarity I am aware, more than at any other time, of how much I lost in those Lyme years.

I want to feel like this all the time.