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rare diseases

By Anthony Vecchione | 04:03 pm | November 19, 2024
The company will use the funds to support people who are managing rare and complex conditions.
By Jessica Hagen | 05:57 pm | May 01, 2024
The new platform for will offer video visits for rare disease diagnosis and longitudinal care.
By Emily Olsen | 12:16 pm | October 11, 2021
Dr. Nadia Chaudhri, a neuroscientist and professor, shared her experience with ovarian cancer on Twitter, showing how social media can be a powerful tool to connect and educate on chronic or serious illnesses.
By Emily Olsen | 02:13 pm | August 24, 2021
The platform lets patients with rare diseases access their medical data and participate in research studies.
By Laura Lovett | 11:45 am | August 21, 2020
After her daughter's PFIC diagnosis, Claire Brinkley searched for a way to connect with other parents with similar experiences and questions. 
By Paul Wicks | 05:04 am | February 28, 2020
Ahead of Rare Disease Day 2020, Paul Wicks, scientific advisor for Ada Health, writes about the potential of digital learning health systems in helping patients receive the right care faster.
By Tammy Lovell | 06:18 am | October 18, 2019
The investment will be used to build a clinical-stage portfolio for rare diseases, including treatments for Fragile X syndrome.
By Laura Lovett | 05:18 pm | February 20, 2019
The three companies announced a slew of pilots employing machine learning, collaborative digital tools and blockchain technology. 
By Laura Lovett | 05:40 pm | October 22, 2018
The London-based startup plans to use the new money to build a patient engagement platform and data analysis tool. 
By Dave Muoio | 01:53 pm | August 20, 2018
RDMD, a Bay Area startup leveraging personal health records to accelerate clinical research of rare diseases, has raised $3 million in seed funding.