Would you like to be part of this innovative and exciting project to deliver a special RARE Kids edition of Rare Revolution Magazine?
If you would like to sponsor or support this project and give Liberty and other young rare disease patients, carers and siblings a strong and powerful voice to be heard then we would love to hear from you.
Contact us now to discuss this wonderful project:
An annual rare disease magazine written for children by children!
Here at Rare Revolution we are passionate about providing a platform where rare disease can find a safe voice in a language that everyone can understand, making it truly accessible. To this end we are pushing the boundaries and leading in information innovation and are teaming up with part of the RareTogether initiative developed by British Paediatrics Surveillance Unit (BPSU) and Birmingham Children's Hospital, Rare Disease Centre to create a very special project.
We are opening up our magazine and letting the children take over once a year to produce an accessible, informative and engaging rare disease publication created specifically for children - by children! Our vision is to create a magazine where children can find information relevant to them, tell their stories in a safe environment, ask questions and take ownership of their RARE stories and experiences.
Our target audience is 8 to 18 years old. With a mix of professional and peer content we will enlist the help of a team of RARE Children to work with us on this special publication. From assistant editor, columnist, blogger, journalist, video content and photographer we want this to be a truly kid centric affair. Our aim is to engage and enlist our child team to help us with content that is relevant to them in the voice that matters - THEIRS!
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Rare Revolution Magazine is a free subscription, quarterly digital magazine. Free subscribe to receive our latest and future issues at www.rarerevolutionmagazine.com