It’s Rare Disease Day!
Happy Rare Disease Day everyone! We have been astounded by all of the engagement we have received for this year’s campaign already. Don’t forget to post your stripy sock photos […]
Happy Rare Disease Day everyone! We have been astounded by all of the engagement we have received for this year’s campaign already. Don’t forget to post your stripy sock photos […]
Happy Lunar New Year! As we welcome the year of the horse, remember to show some support for their stripey counterparts. As you may know, there is an old rhetoric […]
Medics for Rare Disease’s new, ultra-compact training video is now available to watch here. In the run-up to Rare Disease Day, 28th February, we are striving to get the video […]
Join Medscape for a live educational session, ‘When to Suspect a Rare Disease in Any Practice Setting’, featuring our very own CEO Lucy McKay. This live-streamed event will take place […]
Join Central and South Genomics for an insightful webinar in recognition of Rare Disease Day, where they will bring together patients, healthcare professionals, and researchers to explore the latest in […]
26 January 2026: Medics for Rare Disease today announced the launch of a mini training video that will help HCPs become more ‘rare aware’ in five minutes. Since 2022, the […]
Rare Disease Day 2026 is your chance to stand with the 3.5 million people in the UK living with a rare disease, and to take one small action that can […]
Thanks so much to everyone for getting involved with this year’s Rare Disease Day! It’s been amazing how many of you have shown your stripes and they all look fantastic! […]
Happy Rare Disease Day! We can finally reveal the special segment recorded with Medscape for Rare Disease Day. We would like to thank everyone involved in making this happen, it […]
With my head hung down, trying to hide my morning face away from the scurry of staff hurrying between the shift changeover, I scan the floor for those familiar patterns; […]