This 100% for a disease that depends on videomicroscopy for diagnostics through to much needed developing therapeutics. Some say 'there's no such thing as bad publicity', especially in rare disease, but disinformation takes even more work to try to tackle. #StopTheSlop #PCDAwarenessMonth

October is #PCDAwarenessMonth 🌍

Primary ciliary dyskinesia (PCD) is a rare genetic condition where cilia in the airways do not move properly. @European_Lung has a range of resources available which healthcare professionals can share with their patients: https://bit.ly/4hPK6oM

💙 October is #PCDAwarenessMonth.

PCD is a rare genetic condition that can affect the lungs, ears and sinuses.

👉 https://europeanlung.org/en/information-hub/lung-conditions/primary-ciliary-dyskinesia-pcd/

Thank you to PCD patient organisations across Europe and beyond for supporting the community.

While #NikonSmallWorldInMotion has been quiet over #CiliaGate, the story has broken mainstream media here in the UK just in time for #PCDAwarenessMonth www.bbc.co.uk/news/article...