Post by CureRare

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๐—ฃ๐—ฟ๐—ฒ๐˜€๐˜€ ๐—ฟ๐—ฒ๐—น๐—ฒ๐—ฎ๐˜€๐—ฒ: "๐—ง๐—ต๐—ฒ ๐—ฑ๐—ถ๐—ฟ๐—ฒ๐—ฐ๐˜ ๐—ฝ๐—ฎ๐˜๐—ต ๐—ฏ๐—ฒ๐˜๐˜„๐—ฒ๐—ฒ๐—ป ๐—ฝ๐—ฎ๐˜๐—ถ๐—ฒ๐—ป๐˜ ๐—ฎ๐—ป๐—ฑ ๐˜€๐—ฝ๐—ฒ๐—ฐ๐—ถ๐—ฎ๐—น๐—ถ๐˜€๐˜" ย  A recent article published by the Odenwaldkreis tells the story behind CureRare and the vision driving the digital tool RareNavigator. It highlights what many families affected by rare diseases experience: long diagnostic journeys, countless detours and years of uncertainty before reaching the right experts. ย  CureRare was founded by Claudio Cinquemani, a father of a child affected by a rare disease, along with two partners. What began as a deeply personal search for answers has grown into a clear mission: to ensure that people living with rare diseases can connect faster and more directly with the right specialists. At the heart of this mission is the AI-powered RareNavigator, a digital solution designed to connect patients, patient organizations, researchers and medical professionals through verified data sources. The tool is being developed in close collaboration with the Center for Rare Diseases of the University Hospital of Bonn (ZSEB) and the University of Applied Sciences of Central Hesse (THM) and is funded by the German Federal Ministry for Economic Affairs and Energy (BMWE). CureRare is also supported by the Mentor Network of the Odenwaldkreis Economic Development Agency. The article shows how innovation emerges when personal commitment, interdisciplinary collaboration and technology come together โ€” with the goal of reducing diagnostic delays and turning hope into tangible support for millions of people worldwide. ย  Read the full article (German): https://lnkd.in/dkamW93r Christoph Meyer zum Alten Borgloh; Jidnyasa Gujar #CureRare #BMWE #ZSEB #THM #RareNavigator #SelteneErkrankungen #unraremeย #PatientAwareness #RareGenetics

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