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, I realised that far too many patients are confused about their diagnoses, their conditions and their treatments. There’s a disconnect between the language that doctors use, and what everyday people understand. This can make you feel incredibly hopeless and anxious at an often very difficult time in your life.
We believe there is a better way. We believe all patients, regardless of age, gender, culture or condition, should have access to medical information they can understand! Everyone should feel informed and empowered, in order to engage with their doctors and be involved in making medical decisions.
This is why MEDICINE X was created.
Dr. Kim Chilman-Blair
Founder, MEDICINE X
About CIDP Xplained
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!
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.
Check out the experts that have been involved with CIDP Xplained!
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.guillainbarresyndrome.org
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.gbs-cidp-nsw.org.au
Kindly supported by
Kindly supported by
We are driven by our promise to save lives and improve the quality of life for our patients and their families, because living with a rare disease impacts more than just one person. We offer support programs and activities and we partner with patient advocacy organisations to improve and expand educational and outreach efforts. We also work with government authorities to ensure patients have access to the medicines they need to live life to the fullest.