“I write about Parkinson’s because clear, honest information changes how people live with it. Confusion is its own kind of burden.”
HOW TO USE THIS GUIDE
You don’t have to read it front to back. Each chapter stands on its own — start wherever you need answers most.
- Just diagnosed? Begin with Part 1 and Part 3.
- Managing symptoms day to day? Jump to Parts 4, 5 and 6.
- Caring for someone with Parkinson’s? Part 10 was written for you.
- In a crisis right now? Go straight to the Helplines & Crisis Support section.
Below, you’ll find the whole guide laid out step by step. Click any chapter to read it.
If you’d prefer to hold it in your hands, it’s also available as a book through selected publishers.
THE GUIDE, STEP BY STEP
Part 1 — Understanding Parkinson’s
Start here. What Parkinson’s actually is, how it affects the brain and body, and what a diagnosis does — and doesn’t — mean for your future.
[Read Part 1 → (Coming soon)]
Part 2 — Diagnosis & Early Signs
The subtle signs that often appear years before diagnosis, how Parkinson’s is diagnosed, and why the process can take time.
[Read Part 2 → (Coming soon)]
Part 3 — Symptoms in Detail
A clear, plain-language tour of both motor symptoms (tremor, rigidity, slowness, balance) and the non-motor symptoms that matter just as much — sleep, mood, pain, digestion, and more.
[Read Part 3 → (Coming soon)]
Part 4 — Movement & Exercise
Why movement is one of the most powerful tools you have, which types of exercise show real benefit, and how to build a routine that fits your life.
[Read Part 4 → (Coming soon)]
Part 5 — Medication & Treatment
How Parkinson’s medications work, what to expect over time, and an honest look at surgical and advanced options like Deep Brain Stimulation.
[Read Part 5 → (Coming soon)]
Part 6 — Nutrition & Daily Life
Food, supplements, and the everyday hacks that make ordinary tasks easier — practical intelligence gathered from people living it every day.
[Read Part 6 → (Coming soon)]
Part 7 — Emotional & Mental Wellbeing
Anxiety, depression, apathy, and the emotional weight of Parkinson’s — why they happen, and what genuinely helps.
[Read Part 7 → (Coming soon)]
Part 8 — Tracking & Journaling
Simple tools and templates to track your symptoms, medication, and daily patterns — so you and your care team can see what’s really going on.
[Read Part 8 → (Coming soon)]
Part 9 — The Kill Parkinson Registry
How your everyday experience can become science. Learn what the Registry is, how it protects your privacy, and how you can help shape the future of Parkinson’s research.
[Read Part 9 → (Coming soon)]
Part 10 — For Care Partners
Written for the people who care for and love someone with Parkinson’s — how to support them, and yourself, with honesty and sustainability.
[Read Part 10 → (Coming soon)]
Part 11 — Practical, Legal & Financial
Navigating work, benefits, travel, and the practical realities of life with Parkinson’s — with specific guidance.
[Read Part 11 → (Coming soon)]
Part 12 — Glossary & Resources
Every term in the guide, explained in plain language — plus helplines, organizations, and where to turn for support.
[Read Part 12 → (Coming soon)]
Parkinson’s disease tracker and Downloads
The download section containing the tools and templates mentioned in the guide for recording treatment outcomes, symptoms, medication and daily routines – for you, your family and your therapists.
This guide is free because of people like you.
We’re a patient-led non-profit with no paid staff. Every contribution goes directly into keeping this guide free, translating it for more people, and building what comes next — including the Kill Parkinson Registry.
If this guide helps you or someone you love, please help us reach the next person who needs it.
