Guest Voice: Fear shadowed my diagnosis, but I’m stronger than ever
Over time, I learned to focus on what I could control
Aranzazu Calzado, known to friends as Zazu, has lived in Houston, Texas, since 1996 after moving from Spain. She was diagnosed with primary progressive multiple sclerosis in 2021 and faces the challenge with resilience, relying on God, family, and friends as her support network. She finds joy in helping others as a pharmacist, and her passions include travel, photography, reading, cooking, and socializing. Zazu hopes to inspire others on their multiple sclerosis journey and remind them they aren’t alone.
When I was diagnosed with multiple sclerosis (MS) in December 2021, it felt like the ground had been pulled out from under me. The news came after years of unexplained symptoms, including fatigue, tingling in my limbs, foot drop, and leg weakness. I’d hoped it was something minor that could easily be fixed. But when the doctor said the words “multiple sclerosis,” my heart sank.
My initial feeling was shock. I’d heard of MS before, but it was always something that happened to other people, not me. The reality of the diagnosis was hard to grasp. I felt like I was in a fog, unable to fully comprehend what it meant for my future. The doctor explained the condition, its potential progression, and the treatment options, but it was difficult to take it all in.
Fear quickly followed the shock. I was scared of what the future held. Would I be able to continue working? How would this affect my relationships? Would I end up in a wheelchair? These questions swirled in my mind, creating a sense of dread that was hard to shake. The uncertainty was overwhelming, and I felt like I was staring into a void.
Sadness was another emotion that hit me hard. I mourned the loss of the life I had envisioned for myself. The dreams and plans I’d made seemed to crumble before my eyes. It was a deep, aching sadness that lingered, making it difficult to find joy in the things I once loved. I felt isolated, as if no one could truly understand what I was going through.
But amid the shock, fear, and sadness, there was also a sense of determination. I knew I had to face it head-on. I started researching MS, learning about the condition, and connecting with others who were living with it. Their stories gave me hope and strength. I realized that while MS was a part of my life, it didn’t have to define me.
Support from family and friends became crucial. Their love and encouragement helped me navigate the emotional roller coaster. They listened to my fears, offered a shoulder to cry on, and reminded me of my resilience. With their support, I began to see that I could still lead a fulfilling life, even with MS.
Acceptance came gradually. It wasn’t easy, and there were days when the fear and sadness resurfaced. But over time, I learned to live with the uncertainty. I focused on what I could control: my diet, exercise, and the treatment plan. I found new ways to enjoy life and set realistic goals for myself.
Being diagnosed with MS was a profound experience that changed me in many ways. It taught me the importance of resilience, the value of support, and the power of hope. While the journey is ongoing, I’ve learned to face each day with courage and optimism, knowing that I’m stronger than I ever imagined.
To submit your own Guest Voice for publication on Multiple Sclerosis News Today, please email your idea to our columns manager at [email protected] with the following included in the subject line: “Guest Voice: Multiple Sclerosis News Today.”
Note: Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Multiple Sclerosis News Today or its parent company, Bionews, and are intended to spark discussion about issues pertaining to multiple sclerosis.
About the Author
Leave a comment
Fill in the required fields to post. Your email address will not be published.