Dx29: Let's reinvent together the diagnosis of rare diseases

I need your help. Did you know that... - rare diseases on average take up to five years to be fully diagnosed? - the price of full genome sequencing has dropped down to just a few hundred dollars? - with the latest advances in genomic analysis and AI we can reduce the time to diagnose a rare disease to few minutes? Julian, the founder of Foundation 29, started this revolution 11 years ago when his second son was born, and he realized his son had a rare disease. The disease was severe and it changed his life and the life of his family forever. When a catastrophic event happens in your life you can either give up or fight. Julian chose to fight. During all these years Julian has dedicated his life to rare diseases. He has created a couple of patient organizations and works in Europe with the most important research organizations. He has done this in addition to his work. You can watch his history on this video

A couple of years ago he founded Foundation 29, a non-profit organization that works to explore how technology can help patients with rare diseases. Diagnosis is his main area of work. We have developed www.dx29.ai to provide a new platform to support physicians in their decision-making process and reduce the time to diagnosis to a few minutes. We need to find patients with rare diseases so we can improve the platform's accuracy. We all might know someone with a rare disease, or a disease with strange symptoms. We need your help. If you anyone that might have a complicated set of symptoms or someone that already has a rare disease please let them know about this platform. This simple gesture could transform the life of millions around the world.