CIDP Xplained


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CIDP Xplained

Through storytelling

Meet Mark

Hi, I’m Mark!

I’ve got CIDP, also known as chronic inflammatory demyelinating polyneuropathy. It took several years to finally find a diagnosis but once I was diagnosed and had the right treatment and management plan under control, I started to feel a whole lot better. If you want to hear more about me and my story, check out the video.

Medicine X Story

Working as a medical doctor, Medicine X founder, Kim Chilman-Blair realized that far too many people are confused about their diagnoses, their conditions, and their treatments. The language that doctors use, and what everyday people understand can be two totally different things.

Here at Medicine X, we believe that everyone should feel informed and empowered so they can engage with their doctors and be involved in making medical decisions. That’s why Medicine X isn’t just another boring and complicated fact sheet – we explain medical issues through stories based on real people. It’s relatable, simple, and gives you the information you need.

We hope this helps you on your journey!

About CIDP Xplained

Real People

The CIDP XPLAINED story is based on a real person – Mark! It reflects his story, his experiences and his advice to others. There have also been lots of people who contributed along the way with their stories and advice. Thanks to everyone who helped create CIDP Xplained!

Our Team

The MEDICINE X team are doctors, artists, and creative writers that all work to make sure of one thing – the information is easy to understand. No more medical jargon! Everything is correct and up-to-date!


Each of the stories we create is different, so there are experts in the field of CIDP that have reviewed the story to ensure it is spot on in terms of medical information.

CIDP Xperts

Check out the experts that have been involved with CIDP Xplained!

Photo of Professor Steve Vucic

Professor Steve Vucic

Senior Staff specialist in neurology, clinical academic and translational researcher

Read more

Photo of Karen Wells

Karen Wells

Clinical Nurse Specialist

Read more

Produced in Partnership With

The Guillain Barre Foundation of Australia is a registered charity which aims to increase public awareness through education and raising funds for the research & treatment of Guillain Barre Syndrome until a cure is found. The foundations main purpose is to advance health by supporting and improving the quality of life of patients and families, and to be recognised as the Australian resource for GBS.

The GBS Association of NSW

The GBS Association of NSW Inc. was formed over 30 years ago by a group of patients and specialists. The associations aim is to support and provide information to GBS/ CIDP patients, their partners, family, friends and healthcare professionals within and beyond the hospital environment.

Kindly supported by

The editorial content of this website is written and developed independently of the sponsor. The information provided by Medicine X is of a general nature and is not intended as a substitute for medical advice. While Medicine X has made reasonable efforts to ensure that the health information contained on the website is accurate and up to date, you should not act in reliance on the information provided and you should always seek the advice of a healthcare professional. Never disregard professional medical advice or delay in seeking it because of something you have read on Medicine X websites, apps, email communications or in our communities. If you think you may have a medical emergency, call your doctor or emergency services immediately.

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