Writing
Essays on what the system
doesn't want said.
Writing about chronic illness, healthcare systems, patient advocacy, and building things when your body has other ideas. From Chronically and rois.life, consolidated here.
Mental health is the missing link in chronic illness
What is patient experience data?
We need more patient voices in MedTech
How public policy can change the mental health space
Patient voices in Digital Health products
All about Inflammation with Dr. Natasha Punia
What inflammation actually is. Why it matters more than you think. And what's happening inside when you feel this bad.
The Mindful Migraine expert
Migraine isn't just pain. It's a system, a pattern, a thing to understand. What changes when you stop fighting it and start learning from it.
Redefining mental health with Vanessa Pott
What mental health actually is, once you stop measuring it against the wrong standard.
Falk Schuster on living with Major Depressive Disorder
What it actually feels like. Not the textbook version. The lived version.
The Medical Anthropologist
What happens when a doctor studies systems instead of just treating patients. Dr. Margret Jaeger on why your healthcare doesn't work.
Samah Atout on war and mental health
What happens when lived experience becomes policy. How trauma, resilience, and the refusal to be silent drive real change.
The Complete Pocket Guide to Medical Appointments
For patients who've been dismissed, confused, or talked over. How to prepare, advocate, and leave with what you actually needed.
The skills nobody taught me to name
Machines handle information. Humans handle transformation.
From medic to patient
Patient engagement is not empowerment
The spoonie tax
Women in healthcare deserve better
Buy a nice mattress and grow old with dignity
Thirty-three doctors
The ABC of Public Speaking
From someone who had to relearn how to speak after years of isolation: what it actually takes to find your voice and hold a room.
The Little Book of Patient Communication
What actually works when clinicians and patients try to understand each other — and why most communication training gets the hardest part wrong.
The Algorithm Will See You Now
What AI can do in healthcare. What it cannot see. And the patients it will abandon if we don't ask harder questions about what we're optimizing for.
What Do Patients Want?
The gap between what patients say and what they actually want — and why healthcare's biggest failure is listening to the wrong questions.
Revolution From My Bed
How chronic illness rewired everything I thought about work, identity, and what it means to build when you're not okay.
Good days are dangerous
The worst crashes come after the best days. Why feeling good is a trap, and how I learned to stop falling for it.
The isolated island of illness
Chronic illness is its own country. Nobody visits. Nobody speaks the language. And the loneliness is the part that almost kills you.
7 lessons I learned from 7 years in bed
Not advice. Not inspiration. Just what became clear when everything else was taken away.
Just get up.
What doctors kept telling me while my heart rate hit 170 from standing. What I learned about rebuilding a body that forgot how to work.
A 5090 Won't Fix This
I realized that even top-tier gaming hardware can't compensate for what chronic illness took from me.
The Metrics We Don't Have
Someone told me 'Revolution from My Bed' helped them while bedbound. I realized I had no way to measure the impact that actually matters.
Building Spoons.world: What We're Learning
The real challenges and breakthroughs in building a patient-side community platform where lived experience becomes data.
What Do You Do?
On the impossibility of fitting into categories when your life is all one work.
The Exoskeleton
Why getting an exoskeleton to manage PEM and exercise intolerance changes everything — and nothing.
Chronically: Where the Honesty Lives
Why chronically.life exists. Essays on chronic illness, patient advocacy, parenting through pain, healthcare, and showing up.
My $350 mini PC beats your $2000 gaming rig and also harms the planet less
The Minisforum U790 APU runs PUBG smoothly, fits on a shelf, costs a fraction of a gaming tower, and might be the future of home gaming nobody is talking about.
Shipping into the void
The specific terror of building something real, making it public, and watching the users not arrive.
I replaced a £600 Apple Watch with a $26 Pine64 and I am fine
The Apple Watch Ultra is extraordinary. The PineTime does everything I actually need. These facts can both be true.
The loneliness nobody mentions and the freedom nobody warns you about
Working alone is both harder and better than everyone said it would be. Mostly at the same time.
Why does everything I love try to kill me now
A semi-serious rant about food intolerances, histamine, MCAS, and how the chronically ill seem to be losing foods at an alarming rate.
How getting smaller saved my digital life
iPhone mini. Mini PC. MacBook Air. The year I stopped hauling a gaming rig everywhere and finally felt like my technology fit my life.
The Entrepreneurial Body Keeps the Score: What Building a Business with Chronic Illness Really Looks Like
The Story That Changed My Life (And Can Change Yours)
Revolutionizing Medical Education: The Empathy Imperative
Why Five Days Changed Everything for Future Doctors
Invisible Illness, Visible Resilience
The Daily Price of Patient Advocacy
Dancing with My Demons to Help Others Find Their Way
Breaking Free from Social Media's Success Theater
Hi, I'm Roi Shternin
Hi, I'm Roi. I help organizations and their teams flourish under uncertainty by building a practical blueprint for resilience
An Exciting Update & A Special Offer
Your next speaker should be a patient.
Managing Energy with Chronic Illness
Revolution From My bed?
Where to start?
Sick of my Sickness.
The Healing Power of Empathy in Medicine
The Way Out
Health IT is broken, Let's fix it.
A Tapestry of Strength: Fostering Collaboration in Patient Advocacy
Every Chronic Illness Has a Mental Health Component
Case managers: The missing link of Healthcare
Invisible Champions: Why Supporting Caregivers Strengthens Us All
Lost in the Labyrinth: Why Health Literacy is the Key to Patient Empowerment
The Duality of Illness: Embracing the Journey While Demanding Recognition
The Bias Silencing Women in Healthcare
Rare Beyond Diagnosis: A Different Perspective on Rare Disease Day
The Forgotten Price of Chronic Illness: A Systemic Approach to Reclaiming Wellness
Beyond the Buzzword: Why Patients Should Be the Pulse of Healthcare Innovation
Reclaiming Empathy in Healthcare
How “Illness Porn” Changed Chronic Illness Forever
The Patient loneliness epidemic
The Invisible Burden of Chronic Illness Loneliness
The Day Mental Health Is As Accessible As General Practice
The Coming Healthcare Revolution
Fighting for certainty: Why Patients are seeking information outside of the doctor's office.
Patient Empowerment: A Year in Review and a Call to Action
Is it time to finally empower Patients?
We are not clients.
Embracing True Patient Centricity in Healthcare
Valuing Patient Time as Much as Clinician Time
The Urge to Prove Our Worth
Chronically Ignored
The Invisible Struggle: The Mental Health Toll of Chronic Illness
The Time is Now to Bring Mental Health into the Mainstream
Learning from Israel's Response to Collective Trauma
A Revolution in Medical Education: The Power of Partnership and Resilience
The Wounds That Do Not Heal: The Trauma of War on the Soul of a Nation
Ableism is everywhere.
Your next speaker should be a patient.
Unlocking the Superpowers of Necessity: Why Chronically Ill and Disabled People May Be Our Best Employees
Unlocking the Superpowers of Necessity: Why Chronically Ill and Disabled People May Be Our Best Employees
It's Time to Acknowledge Invisible Illness and Disability
It's Time for a Chief Patient Officer in Every Healthcare Organization
It's Time to Lift the Taboo Off Mental Health
Is it Our Job to State Our Disabilities?
Patients are experts too.
The Isolated Archipelago of Illness
Harnessing the Power of Patient Experience Data, Patient-Reported Outcomes, and Patient Empowerment in Chronic Illness Management
Health Literacy: The First Step to Empowered Self-Management
Introducing Patient Schools: Empowering Chronic Patients through Education
The Importance of Having Your Own Resiliency Toolkit
Empathy, Resilience, and Patient Empowerment in Medical School
Empathy Training: A Promising Intervention for Improving Empathy Skills
Uplifting the Human Side of Healthcare
Patient Empowerment: The Power of Post-Traumatic Growth
Empowering Change: Empathy, Equity, and Resilience in the Face of Chronic Illness
Empowerment, Resilience, and Advocacy: Transforming Patient Experiences Worldwide
Paternalism to Empowerment
Issue 3: Revolutionizing Healthcare through Empathy, Innovation, and Patient Involvement
Empowering Voices: Navigating Compassion, Advocacy, and the Patient Experience
Chronicles of Resilience: Empowering Voices in Chronic Illness
How to manage expectations as a Chronically ill patient? (and how to support them as an HCP)
Falling from Grace: Rising Beyond Relapse as an International Public Speaker with Chronic Illness
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