Edmund Lau
Psoriasis
Singapore

Living with psoriasis has been one of the most defining experiences of my life. It has shaped my resilience, tested my perseverance, and transformed how I view health, productivity, and advocacy. While the journey has been far from easy, it is a story of survival, breakthroughs, and the belief that chronic illness should not define or limit a person’s potential.

The Early Struggles: Life with Psoriasis

For years, psoriasis controlled nearly every aspect of my life. Painful, inflamed patches covered my scalp, limbs, and body, making even simple daily activities uncomfortable and exhausting. Sleep was rare, energy was fleeting, and each flare-up chipped away at my physical and emotional strength.

More than just a physical battle, psoriasis deeply impacted my self-image and mental health. I often hid my skin beneath long sleeves and avoided social situations. The stigma surrounding visible skin conditions made things even harder. I felt isolated, wondering if I could continue pursuing my professional dreams while managing a disease that left me so depleted.

Despite this, I held onto my passion for teaching and learning. As an Associate Lecturer in universities across the US, UK, and Australia, I found joy in educating and inspiring students. But the reality was harsh. Some days, I could barely manage an hour of effective teaching before needing to rest. My condition constantly interrupted my work and sapped my strength. I tried every available treatment—creams, lifestyle changes, dietary shifts—but nothing brought lasting relief. Each failed attempt added to my frustration.

The Turning Point: Biologic Therapy

Everything changed when I was introduced to biologic therapy. Initially skeptical after so many disappointments, I soon discovered that biologics target the root causes of inflammation rather than just masking the symptoms.

The results were life-changing.

For the first time in years, my skin cleared. The pain, fatigue, and itching vanished. I felt free—not only physically, but mentally and emotionally. Suddenly, I could teach for 10 hours without crashing. I became fully present for my students, more interactive, and more energized. My transformation didn’t go unnoticed. I was not only back—I was better.

This recovery reignited my drive, confidence, and purpose. But it also gave me clarity: no one should have to suffer in silence or be denied access to the treatment that gave me my life back.

From Patient to Advocate

With my health restored, I felt a responsibility to speak up for others. Too many people with psoriasis and other chronic conditions are still fighting in silence—unable to access life-changing therapies because of cost, awareness gaps, or healthcare system failures.

My journey became about more than just overcoming a personal struggle. It became a mission to advocate for equitable healthcare, to educate others about psoriasis, and to push for change. Through my work with global patient organizations, I have had the privilege of sharing my story at international conferences, collaborating with healthcare professionals, and engaging with policymakers to elevate the conversation around chronic diseases.

Becoming a 10x Productive Chronic Patient

Today, I proudly call myself a “10x Productive Chronic Patient”—not because I’ve defeated my illness, but because I’ve learned how to thrive alongside it. I’ve found strength in vulnerability and purpose in adversity.

My commitment to lifelong learning continues to fuel this journey. In January 2025, I completed a Master’s in Health Economics, Management and Policy at the University of Newcastle. I have since been accepted into a Doctorate in Business Administration (Health) at University College London, where I aim to deepen my impact on healthcare systems and policy.

In my advocacy roles—as a Global Psoriasis Ambassador for the International Federation of Psoriasis Associations (IFPA) and Advisory Board Member of the World Patients Alliance—I work to improve treatment access, shape policy, and amplify patient voices worldwide. These roles allow me to engage directly with healthcare stakeholders and drive real change in how chronic conditions are managed.

A Message to Fellow Patients

To anyone living with psoriasis or another chronic illness: I see you. I know the pain, frustration, and hopelessness. But I also know that transformation is possible—with the right treatment, support system, and mindset. You do not have to suffer in silence. Advocate for your health, seek the care you deserve, and surround yourself with people who understand your journey.

I owe deep gratitude to my family caregivers, whose unwavering love and support carried me through the darkest times. Their strength helped me find my own, and their belief in me never wavered.

Looking Ahead

This is just the beginning. My mission is to continue advocating for patient-centered healthcare, raising awareness, and proving that chronic illness is not the end of the story—it’s a chapter that can lead to something powerful.

I invite healthcare professionals, patients, policymakers, and caregivers to join this movement. Together, we can dismantle the stigma, expand access to care, and build a world where no one is left behind because of their health condition.

Let’s keep pushing forward—for ourselves, for each other, and for a healthier, more inclusive future.

“Reclaiming Life: A Half-Century with Chronic Pain"