Join the community in coming together to raise awareness for #RareDiseaseDay2026 at our Joint Nation online event on Thursday 5 March, at 10.00 - 12.00. Register your place now: www.eventbrite.co.uk/e/rare-disea...
#RareDiseaseDay #RDD2026 #Rarequity
🚨New: Blog from our colleague Dan O'Connor for #RareDiseaseDay: Prevention can be the most powerful treatment of all.
A timely read highlighting why equity & prevention are vital. @geneticallianceuk.bsky.social
🔗 Read more: www.abpi.org.uk/media/blogs/...
#RareDiseaseDay2026 #rarequity
Our colleague Dan O'Connor attended the packed @geneticallianceuk.bsky.social Rare Disease Day event yesterday. 🧑🤝🧑
Great to see so many people calling for equity for rare diseases.
Download the @geneticallianceuk.bsky.social's advocacy pack 👉http://bit.ly/4rp81yB
#rarequity #RareDiseaseDay
There's only one week to go until #RareDiseaseDay. Did you know that only 1 in 20 rare conditions have an approved treatment or medicine? With there being over 7,000 identified rare conditions, that leaves thousands of conditions with no available treatments.
#Rarequity
Did you know 1 in 17 people will be affected by a rare condition at some point in their lives?
Take a look around you and have a think about how many people that really is! Help us spread the word so changemakers know why they should #CareForRare.
#RareDiseaseDay #Rarequity