Tag: resilience

  • Beyond the Machine

    Beyond the Machine

    Beyond the Machine: The “How” and “Why” of Living Strong on Dialysis.

    If you saw me on the street, you wouldn’t know I’m a kidney patient. You’d see a woman running an NGO, managing digital strategies, and advocating for a nation’s health.

    But behind that strength is a very specific, very disciplined “Hustle.”

    Too often, kidney advocacy stays at the surface level: “Drink water. Check your BP.” But what happens when the “worst-case scenario” becomes your daily reality? What happens when you are sitting in that dialysis chair three times a week?

    I want to talk about everything—the parts people are too scared to discuss.

    The “How” of the Access (Fistula vs. Catheter)
    Many patients start with a “line” in their neck or chest. It’s scary, it’s prone to infection, and it feels like a constant reminder of illness. The “strong” move is the Arteriovenous (AV) Fistula.

    • Why? It’s your own blood vessels. It’s under the skin. It’s safer for long-term use.
    • The Secret: It’s not just a surgery; it’s a lifeline. Protecting that arm becomes your new job.

    The “Why” of the Lab Detective
    You cannot wait for your doctor to tell you that you’re in trouble. You have to learn to read your own blood work.

    • Potassium & Phosphorus: These are the silent enemies. If your labs are high, your heart and bones pay the price.
    • The Power of “No”: Being strong means saying no to the “small water” or the “extra salt” even when you’re craving it. Discipline is the only way to feel “healthy” on this journey.

    The Myth of the “Concoction”
    In Ghana, when the diagnosis hits, everyone has a “cure.” A root, a herb, a tea. Let’s be clear: These things often finish what the disease started. Advocacy means being brave enough to tell people that the hospital—while expensive and tiring—is where the science of survival happens.

    My Message to You: I am healthy and strong not because I’m “lucky,” but because I am loyal to my treatment and it’s just by grace. I manage my blood pressure like a business. I treat my diet like a mission.

    If you are on this road, don’t just “endure” it. Master it.

    I’m Hilda Addo, and I’m here to show you that kidney failure is a turning point, not the end of the story.

  • February Reflections: Holding On, Moving Forward

    February Reflections: Holding On, Moving Forward

    As February ends, let’s remember that protecting our kidneys is not only for this month — it’s a lifelong journey. So we keep going, step by step, day by day.

    To everyone going through something — maybe family pressure, work stress, or life’s struggles — hold on small. Breakthrough is coming, slow but sure.

    If you are walking the journey of diagnosis, whether kidney disease or any other chronic illness, remember that with God, all things are possible.

    If you are waiting for marriage or the fruit of the womb, don’t lose hope. God is still in the miracle business.

    And to those already living with chronic disease or kidney failure, you are not alone. You are stronger than what you are facing. Don’t let the situation write your story for you.

    This month shouldn’t just end like that — let it leave impact in our lives and in how we take care of ourselves.

    Next month is Kidney Disease Awareness Month, and we go again, by God’s grace.

    “God is our refuge and strength, a very present help in trouble.” – Psalm 46:1

    You are worth more than your current situation. Don’t give up.

    Blessed weekend ahead 🌿

    My name is Hilda Addo, and I’m your kidney disease advocate.

  • From Diagnosis to Determination

    From Diagnosis to Determination

    PART 1 — The Dreams I Started With

    Growing up, I had big dreams.

    Dreams so big I couldn’t imagine who I’d be if I didn’t reach them.

    So I studied hard. I planned carefully.

    I wanted to become someone I could look back on and say,

    “Well done, Dr Hilda. You made it.”

    But life had its own plans.

    “For I know the plans I have for you… plans to give you hope and a future.”

     Jeremiah 29:11

    While I was still in school, I had already pictured my life ahead, university, success, the future I had carefully imagined.

    What I didn’t know was that life doesn’t always ask for permission before it redirects you.

    One thing I’ve learned on this kidney journey is this: it can be silent.

    No loud warnings. No obvious signs.

    Sometimes the quiet things we ignore are the ones that change everything.

    One day, my mum came to visit me.

    She looked at me closely and asked,

    “Hilda, are you okay?”

    I laughed it off.

    Mum, I’m fine. I just want to finish school, move forward, and make you proud.

    But life was already whispering a different story.

    I didn’t feel sick.

    Nothing felt wrong.

    The only thing that seemed off, I brushed aside as “normal.”

    Until one weekend at home, when everything shifted.

    A hospital visit.

    Concerned looks.

    Doctors asking questions that suddenly felt heavy.

    I remember sitting quietly, waiting for my mum, watching unfamiliar preparations unfold, and realizing that this wasn’t just a routine check.

    Today, when people hear my story, they’re often surprised that I’m living with kidney failure.

    But my response is simple:

    With God, all things are possible.

    That moment marked the beginning of a journey I never imagined, one that reshaped my dreams, my strength, and my purpose.

    And trust me…

    what came next changed everything.

    To be continued……

    My name is Hilda Addo, and I’m your kidney disease advocate.