News and stories

With a team that spans universities, NHS sites and patient-advocacy groups, and aims to improve every aspect of rare respiratory research and patient care, there’s always something going on at the LifeArc Centre for Rare Respiratory Diseases.

Roadmap for Rare

Roadmap for Rare

Our Roadmap for Rare event brought together rare disease experts and advocates to ask whether we can move fast enough, and together enough, to drive real progress for people affected by rare conditions.

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Coming together for rare: two days, three events, one goal

Coming together for rare: two days, three events, one goal

What a week of community, conversation and collaboration! Over two days and three events, we brought researchers, advisors, partners and clinical colleagues together in London to celebrate successes, share ideas and look to the future. As always, we had our eyes on...

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New Events

New Events

We’d like to spotlight on PCD Awareness Month – October 2025This October, some of the Centre’s researchers will join partners across Europe in raising awareness of Primary Ciliary Dyskinesia (PCD), a rare and often under-diagnosed condition.  The month is about: A...

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Annual Gathering

Annual Gathering

“From launching our first Lived Experience Advisory Board to preparing the foundations for the UK’s first rare respiratory disease biobank, it’s been a busy summer.  On 2–3 September 2025 at Mary Ward House London, we will host our first Annual Gathering at Mary Ward...

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Our First 12 Months of Success

Our First 12 Months of Success

Since launching in September 2024, the LifeArc Centre for Rare Respiratory Diseases has made significant strides in establishing a strong foundation for discovery, collaboration, and impact. One of our early successes has been building the Centre’s team. Across the UK...

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