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Myasthenia Gravis Xplained

Through storytelling

Meet Jayde

Hi, I’m Jayde!

I’ve got Myasthenia Gravis also known as MG. MG has affected me and a lot of the things that I can do but it also hasn’t stopped me from being able to do the things I love. Check out my video to find out more about my journey with MG.

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

About MG Xplained

Real People

The MG XPLAINED story is based on a real person – Jayde! It reflects her story, her experiences and her 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 MG 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 MG that have reviewed the story to ensure it is spot on in terms of medical information.

MG Xpert

Check out the expert that has been involved with MG Xplained!

Photo of Dr Stefan Blum

Dr Stefan Blum PhD

Consultant Neurologist

Read more

Produced in partnership with

Australia Myasthenic Association in NSW Inc

The Australia Myasthenic Association was formed in 1982 to provide patient support for myasthenic sufferers and their friends and families. If you have just been diagnosed or you have lived with the condition for a while, its nice to know you are not alone. The association allows members to communicate with people having similar experiences through a Facebook page, and attend calendar events. Please visit the website for more details.



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.

If you are engaging with Medicine X please note that you’re agreeing to our Terms and Conditions and our Privacy and Data Policy.

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