Subscribe Now

By entering these details you are signing up to receive our newsletter.


Meet the team


Rebecca Stewart

Rebecca is our co-founder and brings 30 years of client care experience and ethos to guide our dedicated team. With a passion for people and building networks, Rebecca has channeled a community approach to realising meaningful, accessible resources and the power of education through compelling story telling.Through the development of the company’s “safe hands” approach, Rebecca is committed to steering responsible and sensitive journalism and is active in driving this message forward.Rebecca is also co-founder and trustee of Teddington Trust, a charity supporting those with the ultra-rare condition xeroderma pigmentosum, supporting people internationally with vital protective equipment, education and health and well-being programmes.


Nicola Miller

Nicola is our uber creative co-founder and editor-in-chief. With a strong background in design and a passion for writing, Nicola is the driving force behind our creative vision, and uses her strategic experience in large-scale project planning to oversee our varied work, including RARE Youth Revolution.Nicola is co-founder and trustee of the charity Teddington Trust, volunteering her time to drive forward their mission—supporting families living with the ultra-rare condition xeroderma pigmentosum. Nicola is also author of the award-winning rare disease children’s book series, Little Ted. When not dedicating her time to rare disease, she is raising her two gorgeous sons, and is a rare mama herself.

Special Editions Editor

Emma Bishop

Emma’s background is in the arts, having completed a diploma in foundation studies in Art and Design and an MA in the history of art and design. She has previously worked in retail merchandising for various fashion brands. Emma’s creative talents, both in design and writing, are always innovative and perceptive to her client’s brief. Emma has a love of painting and sketching, but these days her artistic endeavors consist more of potato printing and making lolly stick people with her children, than painting watercolours!

Digital Editor

Geoff Case

Geoff is our digital editor. He graduated from Cardiff University with a degree in English literature and a postgraduate certificate in applied linguistics. Previously a teacher, he worked in education for nearly 20 years. He now uses his passion for reading and writing—and a keen eye for detail—to support others in telling their stories. He takes great pride and pleasure in working within the rare disease community. When he is not working, he enjoys the great outdoors and spending time with his family.

Business Development Associate

David Rose

David is our very suave and never-lost-for-words business development associate. He is a business economics graduate, who was diagnosed with occipital horn syndrome in 2016. David is the only known person in the UK with this syndrome. He is passionate about sharing his health journey, in the form of writing, advocacy and public speaking and also working with clients to share their journeys and raise their profiles through communication strategies. David is a keen Leyton Orient football fan, who regularly goes to games with his dad. In his spare time, you'll often find him planning his next adventure.

Team and Communities Associate

Rebecca Pender

Rebecca, also known as Becky, lives in Glasgow and, among other things, is mum to four young girls. Her eldest daughter lives with not one but two rare genetic conditions making her the only child worldwide with both. With a background of over 13 years in customer service, Becky loves nothing more than curating relationships with like-minded people across the world, making her the perfect fit to look after our charity and media partners as well as our social media channels. When she's not working, she loves a good box set or making memories with her daughters. You can usually find her with a cup of coffee in hand.

Editorial Assistant

Charlotte Cooper

Charlotte Cooper has an autoimmune condition, which she was diagnosed with during her undergraduate degree at the University of Plymouth, where she studied publishing. Charlotte went on to do a master’s in publishing. During her MA, Charlotte undertook a work placement at Rare Revolution Magazine, which led to a part-time position while she completed her studies, focusing on neurodiversity representation in literature. Having completed her MA, Charlotte now works full-time here at Rare Revolution Magazine as our Editorial Assistant who is never without a coffee beside her. When Charlotte is not working, she loves being out in nature on countryside walks in her Devonshire hometown or on Dartmoor, and likes to spend her evenings reading magical realism or crime novels.

RARE Youth Intern

Katie Callaghan

Katie is a well known face in the RARE Youth space having been a regular guest blogger and she also runs Cards for Bravery which encourages people to make cards for hospitalised children. Katie lives with Ehlers-Danlos syndrome and chronic intestinal pseudo-obstruction. She is passionate about transition from paediatric to adult care and has written and spoken publicly several times on this topic. Katie will lead on our Genomics and Relationships project. She loves to read A LOT and enjoys exercising her creative streak.
Skip to content