Top Tweets for #PCDLive
And we're off! Another #PCDLive underway.
This time we're joined with Kait and Emma with their talk "Stepping up to the plate"
#diet #nutrition #healthyliving #healthylifestyle #PCD #PrimaryCiliaryDyskinesia

This Thursday! Don't miss out on another amazing #PCDLive!
This month we have Kait and Emma who explain why nutrition is so important in PCD.
6.30pm start on zoom! Sign up here: https://t.co/KCxYs0ql1q

This month on PCD Live we are focussing on nutrition and it's influence on PCD.
Join us online with Kait Fitzgerald and Emma Farrell at 6.30pm on Thursday 25th May!
Sign up here:
https://t.co/KrvEfHB7uo
#PCD #PCDLive #Nutrition #Diet #HealthyLiving #Healthy
Don't forget to sign up to our next PCD Live on Thurs 27th April!
#PCD #mentalhealth #PrimaryCiliaryDyskinesia #PCDLive
This month on PCD Live we are focusing on Your Mental Health with Dr Anne Griffiths and Tami Vance.
Join us on Thurs 27th April at 6pm! (UK time!)
#PCD #PCDLive #PrimaryCiliaryDyskinesia #mentalhealth #support
https://t.co/y9QOpdjalR
This month on PCD Live we are focusing on Your Mental Health with Dr Anne Griffiths and Tami Vance.
Join us on Thurs 27th April at 6pm! (UK time!)
#PCD #PCDLive #PrimaryCiliaryDyskinesia #mentalhealth #support
https://t.co/y9QOpdjalR
Next up on #PCDLive we have Dr Mary Carroll speaking on #antibiotics
What are antibiotics? Why do we use them? How do we decide which are the best ones to use? What is antibiotics resistance?
Join us to find out the answers to these questions & more:
https://t.co/ZJrdLXxIpP
Tomorrow on PCD Live we have the fantastic @ferrer_mallol from @aparitohealth discussing PCD-ENGAGE!: the first patient-led clinical trial for PCD.
Don't miss it!: https://t.co/5aHdRGWv4O
#digitalhealth #lung #rare #raredisease #pcd #pcdlive #PrimaryCiliaryDyskinesia
Next up on PCD Live is PCD-ENGAGE with Elisa Ferrer (@ferrer_mallol)
Join us on Thurs 23rd Feb:
https://t.co/5aHdRGX2Um
#PCD #PCDLive #PrimaryCiliaryDyskinesia #scicomm #lunghealth #digitalhealth @aparito
Missed our last PCD Live? Good news! We recorded it and it's now available to watch!
PCD Live: Your genes have style with Prof Jane Lucas (@JaneSLucas1): https://t.co/YIA5JbizmB
@JaneSLucas1 #PCD #PCDLive #genetics #genomics #rare #raredisease #PrimaryCiliaryDyskinesia
Join us on Thurs 23rd Feb to learn about PCD-Engage: the first ever non drug-based clinical trial, built by people with PCD, for people with PCD.
https://t.co/5aHdRGWv4O
#pcd #digitalhealth @aparitohealth @ferrer_mallol #PrimaryCiliaryDyskinesia #PCDLive #health
Cilia or pizza?
Great talk by @JaneSLucas1 on #PCD and how your particular genetics might affect the severity your PCD symptoms.
#cilia #primaryciliarydyskinesia #tem #microscopy #pizza #support #scicomm #PCDLive

Is it really a #PCD talk without some high speed video microscopy? @JaneSLucas1
#PCDLive #hsvm #cilia #PrimaryCilliaryDyskinesia #support #community #genetics

So excited for our first PCD Live of the year! We've just started with the fabulous @JaneSLucas1
#PCD #PCDLive #Primaryciliarydyskinesia #genetics #scicomm #support #community

NEXT WEEK! Don't delay - sign up today!: https://t.co/UoakfSIhTw
@JaneSLucas1 #PCD #PCDLive #PCDSupportUK #PPIE
Please welcome back #PCDLive! First up for 2023 is @JaneSLucas1 with "Your genes have style" on Mon 30th Jan.
Have you ever wondered if the gene that causes your family’s #PCD makes a difference to the symptoms? Join us to find out!
Sign up: https://t.co/3sC6Gd2cgb

Please welcome back #PCDLive! First up for 2023 is @JaneSLucas1 with "Your genes have style" on Mon 30th Jan.
Have you ever wondered if the gene that causes your family’s #PCD makes a difference to the symptoms? Join us to find out!
Sign up: https://t.co/3sC6Gd2cgb

Want to know more about #bronchiectasis and #PCD? Check out @ProfJDChalmers chatting about it at one of our #PCDLive events!
https://t.co/IOtde8R6DK
#WorldBronchiectasisDay #PrimaryCiliaryDyskinesia
Loving dogs vs mops in this month's #PCDLive!
@Cellfie3 #PCD #Diagnostics #TEM #PrimaryCiliaryDyskinesia #Rare #RareDisease

Missed PCD Live: "That's rare, I doubt you have it" part 2? We got you! It's on our YouTube to watch now!: https://t.co/EkcklGyTx5
#PCD #Rare #RareDisease #Genetics #Lung #Diagnostics #cilia #PrimaryCiliayDyskinesia #community #PCDLive @LucyD28
Missed @ProfJDChalmers discussing #bronchiectasis and PCD? No worries - the recording is up on our YouTube!👇
https://t.co/P2iD2nzTmS
#Rare #RareDisease #PrimaryCiliaryDyskinesia #PCD #PCDLive
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