Funding life saving research for Primary Ciliary Dyskinesia - donate today and help us find a cure!

Joined January 2022
6 Photos and videos
PCDresearch retweeted
Excited to be at the Rare Diseases Industry Accelerator Day « getting cilia moving » organized by @PCDresearch in London today. Amazing line up of speakers. It will be a great day! pcdresearch.org/gettingcilia…
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PCDresearch retweeted
That's a wrap on this year's @beatpcd @ErnLung meeting! Thank you @mgoutaki @Shoemelia for your efforts and growing this motivated community 😊👏 See you tomorrow at #ERSCongress
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PCDresearch retweeted
7 Jul 2023
Last night we hosted the official launch of our #RareDiseaseTranslational Challenge. We'd like to say a huge thank you to those who attended the reception and thank our speakers for delivering inspiring talks throughout the evening. lifearc.org/strategy/rare-di… #RDTC #LifeArc2030
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PCDresearch retweeted
NATA is proud to support #RareDiseaseDay 2023, working with @EpilepsyRUK, @ActionforAT and @PCDresearch to translate research into benefits for patients with #raredisease. rarediseaseday.org #NucleicAcidTherapies #oligotherapeutics
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Today is #RareDiseaseDay! We are proud to participate in this campaign to raise awareness of rare diseases. The ultimate aim is to reach equity in social opportunity, healthcare and access to diagnosis for all people with a rare disease. This all starts with raised awareness!
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There is still time to submit an application for this exciting project! We are looking forward to reading the applications 📝
Together with the MRC funded Nucleic Acid Therapy Accelerator (NATA) we are delighted to inform you that we will fund a two-year post-doctoral fellowship (£200,000) to start Q3 2023. Please read on for more details! 1/6
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Together with the MRC funded Nucleic Acid Therapy Accelerator (NATA) we are delighted to inform you that we will fund a two-year post-doctoral fellowship (£200,000) to start Q3 2023. Please read on for more details! 1/6
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We are now looking for specific project proposals from people who would like to be a supervisor. If you would like to submit a proposal, please contact me (Dr. Harriet Holme) at: pcdresearch@outlook.com. 5/6
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To be eligible, any overseas supervisors will need to partner with a supervisor based in the UK. The deadline for submissions is the 28th February, 2023. We look forward to reading your exciting proposals! 6/6
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Ever wondered what your donations are used for? This is a quick insight into what your donations can do! 👇 #PCD #PCDresearch
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If you would like to donate, use this link: checkout.justgiving.com/c/32…

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We attended the @beatpcd conference this weekend and it was fantastic to hear from all of the researchers, patients and support groups from around the world. We gave a quick intro to our charity, please get in touch if you have any questions! #PCD #BEATPCD #PCDresearch
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Watch our latest video to find out about what causes PCD 👇 If you would like to donate, please use this link: checkout.justgiving.com/c/32… Please also share our charity with your own network, raising awareness helps us access new resources! #PCD #PCDresearch
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You can help raise money for PCD Research by donating online #JustGiving justgiving.com/campaign/PCDR… #londonlandmarkshalfmarathon #llhm2023 #pcdresearch

PCDresearch retweeted
16 May 2022
Many of you will have noticed a new charity recently, called @PCDresearch . We're excited to work alongside each other to improve the lives of people with #PCD. A quick guide to what each of us do! PCD Support UK: pcdsupport.org.uk/ PCD Research: pcdresearch.org/
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My friend Ian Brooks is fundraising for PCD Research. Check out their @JustGiving page and please donate if you can. Thank you! #JustGiving justgiving.com/fundraising/i…