RDMD is building a platform for data sharing between patients with rare diseases, doctors and researchers.
RDMD aggregates and analyzes medical records and sells the de-identified data to pharmaceutical companies to help them develop medicines. In exchange for access to the data, patients gets their fragmented medical records organized into an app they can use to track their treatment and get second opinions.
- Nancy Yu
- Onno Faber
- Clinton Moore, @CystinosisCRN Board President, is featured in this full-length documentary as he shares their exper… https://t.co/J9UJlpT3gi
- Meghann learned her son was diagnosed with Niemann-Pick disease type C1, a condition with only 500 known cases in t… https://t.co/RA7RZtrPqV
- The diagnosis of their daughter Iris was unexpected, but Douglas & Christine became advocates. They joined RDMD to… https://t.co/2MqEqAINm9