When post-viral ME/CFS first appeared in my life over 30 years ago, it was like a sudden, uninvited guest that turned everything upside down. The plans I had carefully laid out—the career, the teaching, the travel—came to a screeching halt. My body, which once felt like a reliable vehicle for my ambitions, became a source of constant limitation.
For many people today, especially in the aftermath of COVID, the experience of long COVID or post-viral ME/CFS can feel like a similar trainwreck. The life you knew, the expectations you had, are suddenly out of reach, and you’re left grappling with a new reality—one that modern medicine often struggles to explain, let alone resolve.
I remember the early days well. The confusion, the depression, the overwhelming frustration that came with the unrelenting fatigue. In the beginning, it was hard to see any way forward. It felt like I was being asked to surrender everything I had worked for, again and again. Every time I hit a new limit, I had to lower the bar, lower it again, and lower it even further. It was a painful process of letting go, not just of my physical abilities, but of my identity and the future I had imagined for myself.
But over time, and through countless moments of surrender, I began to see that while the path I had planned was no longer possible, there was another way forward. It was a quieter path, more inward, but it was no less valuable. Writing became my outlet, my way of contributing to the world, even while living in solitude and spending much of my time in bed.
For those of you reading this who are newly facing the reality of post-viral ME/CFS, I want to acknowledge that this is not an easy journey. It’s okay if you need to take breaks, both from reading and from the mental and emotional load of processing what this diagnosis means. Be gentle with yourself, and if you find the post too long, take it in pieces, come back when you’re ready. The key is to pace yourself, in life and in reading.
Surrendering to a New Reality
One of the hardest lessons I had to learn was surrender—over and over again. Post-viral ME/CFS teaches you that you can’t control everything, no matter how hard you try. Every time I felt like I was getting close to managing the illness, there would be a setback. My energy would crash, and I’d find myself in bed for days or weeks at a time. At first, it felt like defeat. I had to give up so many aspects of life I’d taken for granted.
But over time, I realized that surrendering wasn’t about giving up. It was about accepting what is, rather than constantly struggling against it. The more I fought the reality of my illness, the more frustration I experienced. Letting go didn’t mean that I had to stop hoping or working toward better health, but it did mean that I had to stop resisting what I couldn’t change in that moment.
Surrendering, in this sense, became a way to make peace with the limits of my body, to find moments of ease even when everything else felt out of control. It was an ongoing practice, one that I still revisit, especially on difficult days.
Navigating Others’ Reactions
In addition to learning how to surrender, one of the most difficult challenges I faced early on was dealing with other people’s reactions. In those early days, many people didn’t even believe post-viral ME/CFS existed. I heard things like, “You just need to drink more coffee,” or, “Have you thought about taking naps?” Even when I was officially diagnosed as disabled by the government, my own mother thought I was just lazy and needed to be more active.
This kind of misunderstanding, disrespect, and dismissal is, unfortunately, a common experience for many who suffer from post-viral ME/CFS. Family, friends, and even doctors would question or deny my experience. I’ve heard stories of doctors telling their patients not to even talk about ME/CFS because it “doesn’t exist.” It was often treated as a garbage-pail diagnosis, or dismissed entirely.
While there is more understanding of post-viral ME/CFS today, the stigma still remains. Making peace with this aspect of the illness has been a long journey. What helped me most was cultivating compassion, not just for myself but for others. As Jesus said, “Forgive them, for they know not what they do.” Having compassion for the people in your life who may deny or diminish your experience is a key part of finding peace.
An Evolving Perspective on Post-Viral ME/CFS
In the early days of my journey with post-viral ME/CFS, I found myself going through what felt like the stages of grief as described by Elizabeth Kubler-Ross. At times, I thought I might be dying, and I cycled through stages of anger, grief, depression, and confusion. Acceptance didn’t come quickly, and it took years of processing and reflection before I could reach that place.
One of the major steps toward acceptance came when I read How to Be Sick by Toni Bernhard. This book resonated deeply with me, and for the first time, I felt like someone truly understood what I was going through. Toni’s reflections on illness gave me a new sense of validation and self-respect, and her practical tips helped me develop a healthier way of relating to my experience. I highly recommend this book to anyone struggling with post-viral ME/CFS.
Then, during a meditation class organized by students of Sogyal Rinpoche, based on The Tibetan Book of Living and Dying, I began to find deeper peace. It was around this time that I discovered a Tibetan sutra titled Transforming Suffering and Happiness onto the Path of Enlightenment. This teaching profoundly shifted my perspective once again.
As I read the sutra, I realized that my anger, frustration, and negative emotions were not only draining my energy but also exacerbating my symptoms. It became clear to me that these stressful emotions were making my condition worse, and that when I was able to relax, let go, and find inner peace, I had greater capacity and longer periods of activity without crashing—or without crashing as severely. This was an important revelation: cultivating acceptance, forgiveness, and inner peace didn’t just feel better, it actually minimized my symptoms.
Shifting Perspective: The Sutra That Changed Everything
One passage from the Tibetan sutra resonated deeply with my experience of post-viral ME/CFS:
“Whenever we are harmed by sentient beings or anything else, if we make a habit out of perceiving only the suffering, then when even the smallest problem comes up, it will cause enormous anguish in our mind.”
This teaching hit home because, for a long time, I had been focusing only on the suffering. Everything in my life had become an enemy—my body, my circumstances, even the people around me. The more I centered my awareness on the pain and limitations, the heavier everything felt. Even the smallest setback would feel unbearable.
The sutra showed me that the more we focus on suffering, the more it grows and colors everything we experience. By recognizing this, I began to understand that shifting my focus away from the suffering and toward acceptance could help me find peace. It wasn’t about denying the reality of the illness, but about no longer letting it dominate my entire perspective.
The true transformation came not only by making peace with suffering but by learning to approach both suffering and happiness with the same equanimity. I had to remind myself that when I’m unhappy, this too shall pass, and when I’m happy, this too shall pass. This reminder became a useful way to stay balanced through the ebb and flow of life—the good days and the bad days, the good months and the bad months.
Additionally, I found comfort in William Blake’s words: “He who kisses the joy as it flies lives in eternity’s sunrise.” It reminded me to appreciate the little moments of happiness, to savor them without attachment, knowing that they, too, are fleeting. This perspective helped me not to be disturbed by the constant changes and to find a sense of peace amidst it all.
Discovering a New Path: Writing as Healing
As I continued to navigate the ups and downs of post-viral ME/CFS, I eventually found a new passion that helped me stay connected to the world and give expression to my inner journey: writing. Although much of my life is spent in solitude, and my physical abilities are limited, writing has become my outlet, a way to contribute and share what I’ve learned.
Through writing, I’ve been able to explore the lessons of impermanence, forgiveness, and acceptance, not just for my own growth but as a way to offer encouragement to others walking a similar path. Chronic fatigue may limit what I can do in the physical world, but it has opened up this creative space where I can still connect, reflect, and contribute.
In this way, writing became not just a coping mechanism but a practice of karma yoga, an offering. It’s a way to kiss the joy as it flies, even amidst the challenges of chronic illness, and to embrace each moment—whether in suffering or happiness—as an opportunity for growth.
🙏🕊️🙏
“He who binds to himself a joy
Does the winged life destroy;
But he who kisses the joy as it flies
Lives in eternity’s sunrise.”
— William Blake, Eternity
Inspirations of Love and Hope 
Thank you 🙏