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Speaker slide for the Mapping Rare webinar. On the left is a portrait of Dr Ellen Moran. She is wearing a navy blazer over a patterned top and standing outdoors with greenery in the background. Text below the photo reads: “Ellen Moran, Scientific Programme Manager.” On the right is the Retina International logo and a text block describing Retina International as a global, patient-led organisation supporting people with inherited and age-related retinal diseases through research funding, advocacy, and education. The Rare Disease Day and Rare Diseases International logos appear at the top. A banner at the bottom reads: “Learn how we’re putting empowerment on the map! Mapping Rare: 17 February at 3 PM CET.”

Speaker slide for the Mapping Rare webinar. On the left is a portrait of Dr Ellen Moran. She is wearing a navy blazer over a patterned top and standing outdoors with greenery in the background. Text below the photo reads: “Ellen Moran, Scientific Programme Manager.” On the right is the Retina International logo and a text block describing Retina International as a global, patient-led organisation supporting people with inherited and age-related retinal diseases through research funding, advocacy, and education. The Rare Disease Day and Rare Diseases International logos appear at the top. A banner at the bottom reads: “Learn how we’re putting empowerment on the map! Mapping Rare: 17 February at 3 PM CET.”

Our colleague, Dr Ellen Moran, will be speaking at the Mapping Rare webinar for Rare Disease Day 2026, sharing perspectives from Retina International.

🗓️ 17 Feb 2026
🕒 3–4 pm CET
🔗 lnkd.in/db8HRPtj

English with live Spanish interpretation and multilingual captions.

#MappingRare #RareDiseaseDay

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