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Bonnie Annis is a breast cancer survivor, diagnosed in 2014 with stage 2b invasive ductal carcinoma with metastasis to the lymph nodes. She is an avid photographer, freelance writer/blogger, wife, mother and grandmother.
Losing an online friend to cancer reminded me that grief is real even across screens and that survivor guilt and gratitude can coexist in the same moment.
I learned about my friend’s death the way many of us now learn life-altering news, alone, with a screen glowing in my hands. I had gone to her Facebook page and her website, expecting an update, a familiar post, a small sign that she was still out there doing the brave, exhausting work of living with cancer. Instead, I felt a heaviness settle in my chest before I saw anything at all. It was intuition, maybe, or the way silence can speak louder than words. An internet search confirmed what my heart already knew. She had died in October. I didn’t even know she was gone.
We met in a Facebook group for women living with breast cancer. Our diagnoses came almost exactly one year apart, hers first, then mine. Her cancer was triple negative; mine was invasive ductal carcinoma: different subtypes, different treatment paths, different risks. But cancer has a way of flattening differences. What rose to the surface instead were the shared human details that mattered more than pathology reports: we both had grown children, devoted husbands and a deep love of art. We understood each other’s fears without needing to explain them.
We never met in person. Still, she became a real friend in every way that counts. We communicated through blogs, texts, emails and letters, small lifelines strung across distance and time zones. We talked about chemo side effects and scan anxiety but also about books, creativity, marriage, faith and the strange beauty that can show up even in the middle of illness. On days when my body felt foreign and my future felt fragile, her words reminded me that joy could still be found in unexpected corners.
Her cancer journey was relentless. She endured chemotherapy twice and, when the cancer returned, faced a third round with a determination that humbled me. Eventually, she was told the cancer had spread to her brain and cerebrospinal fluid. The prognosis was devastating: two to four months to live. Yet she kept fighting, not in a loud or dramatic way, but with a quiet courage that showed up in her willingness to keep living fully, even as the odds narrowed. I believed she was still doing OK. I believed there would be more time.
There wasn’t.
Grief is complicated when the relationship exists primarily online. There is no funeral invitation in the mail, no shared casseroles, no familiar faces to gather with and say, “Did you know her like I did?” The world keeps moving, unaware that a person who mattered deeply to you is suddenly missing. It can feel illegitimate to grieve so intensely for someone you never hugged, never sat across from at a coffee shop. But the grief is real because the relationship was real.
What broke my heart most was not just her death but the unfinishedness of it all. I never got to tell her how much she meant to me. I never got to say goodbye. I never got to thank her for helping me find joy on some of my darkest cancer days. Cancer already takes so much: health, certainty, peace of mind. In this case, it also took my chance to express gratitude while she could still hear it.
As a cancer survivor, her death stirred fears I work hard to keep in check. When someone who walked a similar road dies, it can feel like the ground shifts beneath your feet. Survival guilt creeps in, uninvited and uncomfortable. Why am I still here when she is not? What does her outcome mean for my future? These questions don’t always have answers but they demand to be acknowledged.
I am learning that grief and survival often coexist. One does not cancel the other. I can be grateful for my life and devastated by her loss at the same time. I can celebrate clean scans while mourning the friend who didn’t get that news. Holding both truths is part of the emotional work of survivorship.
There is also a lesson here about presence and urgency. Cancer friendships tend to skip small talk. We go straight to what matters. And yet, even with that depth, we sometimes assume there will be time later to say the most important things. Her death reminds me that “later” is never guaranteed. If someone has walked with you through illness, fear or grief, tell them now what they mean to you. Say it plainly. Say it often.
Though I never got to thank her directly, I am trying to honor her in the way I live. When I encourage someone newly diagnosed. When I choose joy on a hard day. When I create art even when my energy is low. Her influence did not end with her life; it continues in the quiet ways she changed mine.
Cancer communities, especially online ones, are made up of fragile threads of connection. People come and go, sometimes without warning. But those connections matter. They hold us up when family and friends can’t fully understand what we’re going through. They remind us that we are not alone in the long nights of worry and the endless waiting rooms. And sometimes, they leave an imprint on our hearts that lasts far beyond the last message exchanged.
If you are reading this as someone living with cancer or loving someone who is, I invite you to pause and consider the relationships that have sustained you along the way. Who has helped you feel less alone? Who has spoken hope into your fear? Reach out while you can. Say the words you might be saving for later.
And if you are grieving an online friend, know this: your grief is valid. Love does not require physical proximity to be real. The bonds formed in shared suffering and shared hope are powerful, even if they exist across screens and miles. It is ok to mourn deeply. It is ok to carry them with you as you continue to live.
I didn’t get to say goodbye to my friend. But I carry her with me — in my gratitude, in my art and in my commitment to live fully while I can. In that way, her life still speaks and her friendship still matters.
This piece reflects the author’s personal experience and perspective. For medical advice, please consult your health care provider.
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