A Journey of Strength and Self-Love: The Real Battle Beyond Cancer. 1400
Battling cancer was, in some ways, easier than looking for a job. I never thought I’d say that, but today, after an experience I’ll never forget, it felt like the truth. Let me share my story with you, and you’ll understand why.
It’s been two years since I fought cancer for the second time. During my treatments, I wore my strength like a shield, and my family was by my side, helping me navigate each painful day. But there’s one thing that has never fully healed: my hair. After all the treatments, my hair never grew back the way it used to. The texture changed. The thickness was gone. And, no matter how many times I tried, I couldn’t get it to look the way it once did.
I’ve worn a head covering every day since then—partly because I’m embarrassed by how uneven and thin my hair has become, and partly because I’m still trying to hide the parts of me that were ravaged by illness. Only a few people have seen me without it: my husband, my immediate family, and a few doctors. Everyone else only knows me as the woman who wears a head cap everywhere she goes.
But here's the thing: I know what kind of person I am. I know that I’m strong. I know that I’m kind. I’m kind to the lady sitting next to me who talks incessantly, not because she’s annoying, but because she has no one else to talk to. I know that she is the reason I kept showing up for treatment even when I didn’t feel like it. She had no one else, and I couldn’t let her go through this alone. That’s the kind of person I am—someone who lifts others up, even when I’m barely holding myself together.
But the world of job hunting has been far less forgiving. Companies, it seems, don’t care about the kindness you show or the strength you possess. They care about how you look, how well you fit into their idea of "professional." And today, on January 31, 2023, I had an interview that made me realize just how harsh and shallow the world can be.
The interview was conducted over Zoom, and I thought it went well—until it didn’t. As I sat there, waiting for the meeting to end, I could hear them talking amongst themselves in the background. They didn’t end the Zoom call properly before they began their conversation, and what I heard next cut deeper than any chemo treatment I had endured. “She had a head cap on. Did she know she was in an interview?” one person said. Another added, “She would look more professional if she showed her hair. I can’t tell what color her hair is.”
Do they know how much my hair is uneven? Do they know I have bald spots? Do they know how embarrassing it is to even think about showing anyone the damage cancer has done to my appearance? No, they don’t. And they didn’t even try to understand. Instead, they judged me—without knowing anything about what I had been through. They didn’t ask, “How are you doing?” or “What’s your story?” They simply looked at the surface, and that was enough for them to dismiss me.
In that moment, I felt my heart sink. I had already faced the terrifying uncertainty of cancer. I had lost so much. I had fought harder than anyone should ever have to, just to survive. And now, the battle was still ongoing—but this time, it was for my self-worth, my dignity. It was a fight I hadn’t anticipated, and yet it felt just as brutal as the one against cancer itself.
The first time I went to the grocery store after completing two years of treatment, I weighed only 93 pounds. As I shopped, I overheard someone whisper, “Does she know she isn’t even going to eat that food she’s buying?” It stung like a thousand needles. How could someone be so cruel, so judgmental, when they had no idea what I had been through? That moment stuck with me, just like today’s interview will.
But today, I made a decision.
Today, I decided that I would no longer hide the evidence of my battle. Today, I decided to wear my history with pride. I had spent so long covering up my journey, but now I realized that hiding it was only holding me back. I would no longer let others’ shallow judgments dictate how I see myself.
My pride had been hurt by their words, but in that pain, I discovered a valuable lesson in self-love. The world may not always understand me. It may not see beyond my appearance, my hair, or the way I dress. But I know who I am. I am a fighter. I am kind. I am resilient. I am worthy. And the people who matter—the people who truly see me—will appreciate those qualities far more than any superficial judgment.
So, today is the last day I will hide behind a head cap. From now on, I will wear my history proudly, and if someone can’t see the beauty in that, then that’s on them, not me. I’ve fought too hard to let anyone else define my worth. I know my worth, and it doesn’t depend on whether I have hair, or whether it’s uneven, or whether I wear a head covering.
Cheers to the unkind folks out there. You may think your judgment hurts us, but in reality, you are helping us kind folks realize just how important we are to others—and how important our purpose remains. You are helping me see that I don’t need to hide what I’ve been through to be accepted. I will stand tall, just as I did when I fought cancer.
Today, I took a step toward loving myself fully—every scar, every imperfection, and every piece of my history. And I will continue to walk proudly, with my head held high, no matter who else chooses to judge me.
Because I know my worth. And that’s all that truly matters.
From Diagnosis to Hope: How a Rare Brain Tumor Led Me to a New Purpose in Life. 489

A few weeks before my nineteenth birthday, I was sitting next to my mom when she pointed out something strange: my left eye wasn’t lining up with my right one. It made me look like I had a lazy eye. We both laughed about it at first—it did look a bit funny, after all. But when I mentioned it to my mom the next day, she decided to take it seriously. She made an appointment with a neuro-ophthalmologist, a specialist who could help us understand what was going on.
We went to the appointment on a busy Saturday. The doctor quickly checked my eye and suggested we come back another day when he could run more tests. We returned a couple of weeks later, and this time, the doctor asked me if I had been seeing double. I hadn’t even noticed it before, but I realized that I had been seeing double occasionally for some time. The doctor told me that my eye problem, which he diagnosed as sixth cranial nerve palsy, could be caused by something as simple as an infection. But, in rare cases, it could be something more serious—like a brain tumor.

He ordered a series of tests: a chest x-ray, blood work, and an MRI of my head. The chest x-ray and blood work came back normal, but when I went for the MRI, I started to worry that the diagnosis could be bigger than just an infection. My mom and I went to lunch afterward, trying to stay positive, and I went home to continue working on my online classes. I didn’t expect to hear anything until the next day, but a few hours later, my mom came into my room looking very upset. She told me I needed to pick up the phone—it was the doctor.
I’ll never forget that moment. My doctor’s voice on the other end of the line was calm but serious. He told me that there was a mass in my brain pressing on the sixth cranial nerve, and he suspected it might be a very rare type of bone cancer called chordoma. It grows at the base of the skull, and while it’s extremely rare, it was the diagnosis he feared. Two days later, right after my nineteenth birthday, I was officially diagnosed with chordoma.
The news was crushing, but I knew that I had to face it head-on. The first step was surgery to remove the tumor, but it wasn’t an easy process. I had complications—like infections and brain fluid leaks—but I made it through the surgery. However, there was still a bit of the tumor left, so I had to undergo proton radiation therapy to ensure it was completely eradicated. It was a tough journey, filled with pain and uncertainty, but I kept going, one step at a time.

In the midst of all this, I was also dealing with side effects. I developed chronic nerve pain, Hashimoto’s disease, and thyroid problems as a result of the treatments, but I refused to let it stop me. I was a freshman in college when I was diagnosed, and despite everything I was going through, I refused to let my dream of earning my degree slip away. I kept studying psychology and music, and I became involved in my college’s choirs, theater, and student life. I wanted to live my life as fully as possible, even though I was facing so many challenges.
Now, as a junior in college, I look back at everything I’ve overcome with a sense of gratitude. I’ve been in partial remission for almost a year, and I’m thankful for every day I get to live. I’m still working hard toward my goals, and I’m now pursuing a Master’s degree in mental health counseling. I want to become a therapist for young people with disabilities, rare diseases, and cancer—people who understand what it feels like to fight for your life. I also dream of performing professionally in my city’s orchestra and choir, and who knows? Maybe I’ll even audition for America’s Got Talent one day.
Through all the pain, the uncertainty, and the setbacks, I’ve learned that life is beautiful, even in the face of adversity. The journey I’ve been on has made me stronger, and it’s helped me find a purpose. I’ve learned the importance of perseverance, the power of hope, and the strength that comes from faith. I’m thankful to the Lord for everything He has done for me, for carrying me through the hardest times and guiding me toward a brighter future.

My story is one of survival, yes, but it’s also a story of transformation. I’ve gone from being a scared, confused young woman with a grim diagnosis to someone who is proud of what she’s achieved and excited for the future. I want others to know that no matter how dark things may seem, there is always hope. There is always a way forward, and the beauty of life can still be found, even in the most difficult moments.
So, here I am, with a renewed sense of purpose and a heart full of gratitude. Life is still a journey, and while I know I’ll face more challenges ahead, I’m ready for them. And with every step I take, I will continue to honor the strength it took to get here and the dreams that lie ahead.