@Mill_lab @beatpcd@PCD_UK@PCDFoundation@PCD_ispm@lunguk @BlfResearch @mrc_hgu Great, thatβs fantastic to hear. We are looking to spread the word to patients all over Scotland and hear about their experiences. Excited to have your support!
We will be in touch shortly. Thanks π
The most used face masks among people with PCD are certified single use masks or reusable fabric masks. More results from the #covid_pcd study on our website https://t.co/1C5E3t3iWO #pcd#covid19#raredisease
Congratulations go to our very own @pcdmum in being awarded a British Empire Medal for her tireless work for the PCD Family Support Group in the Queenβs New Yearβs Honours list!π₯³
More info: https://t.co/3qroL3adOs
#PCD@lunguk@EuropeanLung#PrimaryCiliaryDyskinesia#champion
A novel real-world validation of two tools (PICADAR and NA-CDCF) that use routinely collected clinical data and help triage the need for primary ciliary dyskinesia diagnostic testing is performed, showing both tools perform well with equivalent performanceΒ https://t.co/fd8O3HjtXD
Well done #PCD community, ππ·π
Your regular participation in the survey is providing important information, so please keep completing the short surveys. If you have #PCD and are not yet involved in this international project, it's easy to join in https://t.co/JPazzoDPpl
Have you participated? Click on the link to see results π€, how many people have participated from each country π΄σ §σ ’σ ³σ £σ ΄σ Ώ and if you havenβt completed the questionnaire, there is a red βparticipate in the studyβ tab! π΄ @PCD_UK@PCD_Scotland@lunguk
https://t.co/YvEnZmlw2j
PCDers we need you! Please complete this questionnaire to help us understand the impact of Covid-19 on people with PCD. The study is open to anyone with PCD around the world: https://t.co/RCRi9ycKV1
#pcd#covid19#primaryciliarydyskinesia#survey#help