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RAREfest2020 promo images

RAREfest20, proudly sponsored by 

Evolution Education Trust logo
Healx Logo

• 28 NOV 2020 • VIRTUAL  festival • 





A FREE, VIRTUAL, interactive science, technology, advocacy and arts exhibition with a rare twist.  Visit exhibition stands, get involved with live demos, talks and panel discussions, view rare art, films and more…

FREE to attend, RAREfest20 is a full day Cambridge Rare Disease Network festival featuring interactive exhibits showcasing cool science, visionary technology, and pioneering organisations improving lives and bringing hope to those affected by rare diseases. 

Alongside the science and technology exhibition there’ll be inspiring talks from experts and powerful patient voices, rare disease inspired art and films.

 For a sneak peek of what you can expect, head to our RAREfest18 pages brimming with cool companies, scientists, tech experts, health pros and patients who took part in our first RAREfest exhibition. RAREfest20 exhibitor, speaker and film programme will be released later in the year.

The RAREfest20 festival aims to provide a window into this relatively unknown area of science and health to spark curiosity.  Join us online for a exciting and informative virtual experience. Open to patients, families, children, students,  healthcare professionals, researchers and companies,. Whether expert or curious, all are  welcome! 

We’re seeking sponsors.
DIscover how your company can be in the spotlight and support the rare disease community

“Be the change you want to see in the world”

Mahatma Gandhi

RAREfest20 Virtual Sponsorship Booklet[1]


Heartwarming, uplifting and informative, the world’s first-ever festival on rare diseases drew huge crowds to the Guildhall over the weekend of November 30 & December 1, 2018.

Mike Scialom, Cambridge Independent Newspaper

The event was absolutely fantastic. It was obvious how much hard work had gone into it and gaining the balance between industry and public interest must have been a tough navigation, which was pulled off unbelievably well.

Steve Smith, Head of Rare Diseases & Gene Therapy

Lots of people we’ve spoken to today are passers-by. They’re out doing their Christmas shopping. That’s wonderful because it means the topic is broadening out to the wider community.

Harriet Gridley, No Isolation AV1 Avatar

Volunteer for #RAREfest20?

Be a  part of our thriving community

There are lots of tasks to do in the run up to and during #RAREfest20. Whatever your skills and availability, we’ll be able to find something to suit you. Come and join your tribe!

If we all got involved, imagine the difference we could make? Don’t just follow us, interact with us and join our thriving rare disease community! There’s lots of ways right here to begin your journey with us…

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