Rare disease stakeholders have converging paths. Our journeys involve each other and intersect at every stage. No two journeys are the same, but the desire for a better tomorrow is universal.
At Beacon, we believe that stakeholders must work together to move the dial forward for rare disease. By bringing individual talents, expertise and knowledge to the table, the community can transform the patient experience without having to reinvent the wheel. The rare community is greater than the sum of its parts when we aid each other and play to everyone’s strengths.
The Rare Disease Showcase
Our Rare Disease Showcase is an event series that celebrates the innovative rare disease projects taking place across the UK and wider world.
Our Showcase series introduces rare disease stakeholders to each other and invites them to share their experiences, work, research and expertise with the wider community.
By sharing and combining the rare community’s skills, we are creating an unstoppable movement that brings real change to those living with rare disease.
Drug Repurposing for Rare Disease Conferences
Our Drug Repurposing for Rare Diseases Conference highlights the role that drug repurposing plays in lowering the cost and time associated with traditional drug development.
We highlight the best examples of rare repurposing in the field to encourage patient groups to get involved in research. Drug repurposing projects are not only led by patient groups, but also by industry, researchers and clinicians. Our Drug Repurposing for Rare Diseases Conference sparks cross-sector conversation and collaboration to ensure that new, repurposed treatments reach patients faster.
Join our Community Mailing List to be amongst the first to hear about our next Drug Repurposing Conference.
The Student Voice Prize (SVP)
The Student Voice Prize is an annual, international essay competition that raises the profile of rare disease within the medical field, particularly with medical students, nurses and scientists who may have never come across rare diseases in their training. Although rare diseases affect approximately 350 million people worldwide, little time is dedicated to them in medical school.
The Student Voice Prize challenges the doctors, nurses and scientists of tomorrow to think about rare disease today. After all, with a lifetime risk of 1 in 17 in the UK, it’s not rare to come across them! We host The Student Voice Prize in collaboration with Medics4RareDiseases. The winner of the competition is published in the Orphanet Journal of Rare Diseases, amongst many other prizes.
Join our Community Mailing List to be amongst the first to hear about our the next Student Voice Prize.
Rarely Heard Podcast
“Rarely Heard” is a brand new podcast for the rare disease community, where each episode delves into what it is really like to live with a rare disease.
We bring a variety of personal perspectives and challenges to light, which have rarely been heard due to fear of judgement, embarrassment or simply society’s noise.
Come with us as we explore the unspoken rare truths around mental health, dating, university and work.