Chapter 15: Beyond Survival: How I Built a Future from the Ashes of a Tragedy

“We are not what happened to us; we are who we choose to become.”

​When the accident occurred, I was in my final semester of a Bachelor’s degree in Economics. After three months in hospitals, I found myself living back with my father, barely mobile and unable to care for my child or my home. It was the height of the COVID-19 pandemic, and while the world was at a standstill, I was learning how to walk again with a physiotherapist.

​In those long hours between exercises, I felt a void. I decided to use the fact that universities had moved online. I contacted my professors, scheduled retakes for my exams, and started studying. It was my escape. Studying distracted me from the dark thoughts; it made me feel less “useless.” While my body was failing, my mind was sharp. I graduated the following year, proud that I had finished what I started.

  1. ​The Poverty of Disability

​By the time I graduated, I had returned to work and launched a fundraising campaign for my surgery in Cyprus. At that stage, a better financial future seemed like a fantasy. I had nothing. My salary was low; I couldn’t even afford medical care for myself or my child. My father had to mortgage our only home to fund half of my treatment. I lived in my child’s father’s apartment and drove his car. I felt like my only possessions were the clothes on my back and my uncomfortable shoes.

​For a long time, I felt a crushing sense of guilt whenever I thought about spending my own salary on myself—whether for clothes or a simple experience. It was as if having needed help for my surgery meant I had no right to a normal life. It took a long time to lift my head from the sand and realize that being a patient didn’t mean I had to stop being a person. During all these years, I was also fighting a long and grueling legal battle for compensation, but the procedures were so slow that I almost lost hope they would ever end.

  1. ​Proving My Worth

​Slowly, I began to adapt to my job. I was back in the same company but in a different position. My colleagues saw me as a person, not a medical file. My managers understood my physical limitations and the need for ongoing treatments. This motivated me. I didn’t want their pity; I wanted their respect. I wanted to prove I was an asset.

​I realized that the sheer logistics of managing my treatments had made me a master of problem-solving and adaptation. If I could manage a shattered life, I could manage a Master’s degree. I completed it with honors and an ease that surprised me. My opinion started to matter at work, my responsibilities grew, and my income moved from “minimal” to “middle.” My self-esteem began to return.

  1. ​The Battle with the System

​In the beginning, I was denied a disability pension for years. I didn’t fit into their “tables and criteria”—my diagnoses were complex, some even unrecognized by local medicine. One day, I decided to fight back. I didn’t hire a standard lawyer to write my appeal. I dug into the law myself, searching for every grain of truth I could hold onto. I wrote my appeal with a dose of sarcasm and bitterness toward the institutions. A few months later, I received the percentage I deserved. It’s a battle I will have to fight every two years, but I’m ready.

​I also learned to navigate the system. When I needed a complex surgery in Belgium, I didn’t turn to fundraising again. Instead, I mastered the institutional pathways and fought until the state agreed to cover the medical costs.

  1. ​The Call that Changed Everything

​One day, while waiting outside a doctor’s office after work, my lawyer called. After years of agonizingly slow litigation, we had a final court decision. We won the case against the insurance company.

​I almost fell off my chair in shock. For years, I had dreamed of what I would do with that compensation. When it finally arrived, the first thing I did was pay off my father’s mortgage and settle my debts to friends. My first “luxury” purchase? A personal laptop.

​Of course, requests for financial help from relatives followed. I helped where I could and started donating to campaigns I believed in. But then, I made a decision for myself. I wanted a home. A sanctuary I could decorate to my own taste.

  1. ​Building “On Green”

​Unexpectedly, my apartment found me. I signed a deal for a property “on green” (still under construction). I know the money won’t be enough to fully furnish it yet, but that doesn’t terrify me. I believe in my ability to grow, and even if I have to take out a loan later, I will have the peace of mind to do it. Winning the case also gave me the stability to afford the travel expenses for my ongoing treatments in Belgium without fear.

​Now, I fall asleep every night knowing that in three years, I will wake up in a place I can finally call home. Those three years will be my “training mission” to fully return to life.

​I’ve proven to myself and the world that I can survive. Now, I’m going to prove that I know how to live. I even got a tattoo to remind me of this path, should I ever lose my way. It feels like waking up from a long lethargy.

​My treatments continue today and will likely last a lifetime. But I refuse to let them stop the rest of me. I’ve learned to manage appointments and surgeries as mere details in my daily routine. Our diagnoses are a part of us, but they are not the whole story.

We are not defined by what happened to us; we are defined by the life we choose to build from the pieces.

I would love to hear your thoughts or share your own journey, please leave a comment below. I’ll make sure to respond to every single one of you – we should support and motivate each other!

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The whole story: The Journey


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