At @Ciitizen we believe change will be driven by the individual alongside the organizations who tirelessly support and advocate for them. This #BreastCancerAwarenessMonth we are highlighting the amazing organizations we work with.
Meet our partners: https://t.co/25eHdkPXiG"
@HealthPrivacy@ciitizen @Invitae For #precisionmedicine to become a reality for all of us, we need patients to have access to their #data from many sources in structured, usable and sharable platforms. AND we need to enable patients to easily share their data with researchers developing #treatments and #cures!
🎉When two of your favorite partners merge. 😍 @Invitae +@ciitizen is great news for #raredisease especially #syngap1 patients who were the first rare group on the platform!
I am very pleased to announce that @ciitizen will be joining the @Invitae family of companies designed to bring the future of healthcare to our users. Ciitizen and Invitae are now jointly advancing patient-centric services and research. https://t.co/6hj6ZYa4gA
In Tania's last six months of life, we crisscrossed the country and saw 23 specialists, none of which had her full #HealthData.
@Ciitizen was born out of a need for accessible #MedicalRecords for all. Learn more about our story in @CBSNews: https://t.co/pEz8uefbPl"
In cancer clinical trials from 2008 to 2018, only 3% of participants were Black. @ciitizen article Demystifying Clinical Trials: Why aren’t more black breast cancer patients participating? https://t.co/3Jya7Nawc8 @mbcalliance
@keatonbedell@nikillinit@ciitizen Spot on. and why we started with cancer because from a data modeling perspective, its arguably the toughest. We've cracked cancer (solid and liquid tumors), expansion from there is easier ;)
@keatonbedell@nikillinit@ciitizen ...yes. Humans don't scale. Only tech does. We spent the first 2.5 years of the company exclusively tackling the unstructured notes challenge with our ML pipeline
Never knew we'd see our technology, #healthcare information exchanges, patient data rights, and Jack Nicholson's face in one post but @nikillinit made it happen. Check out his write up of Ciitizen below! 👇 #HealthRecords
Welcome to Ciitizen Rare Disease Week!
1 in 20 people will live with a rare disease at some point in their life and the majority do not have a cure.
Watch @nashafitter1 and Elli explain why we should all care!
#rarediseaseday#WRDD2021#ciitizen
https://t.co/lGQQzNIFeV
"Systems too often refuse to share data because they fear their patients will be poached. This mentality has to be changed because it endangers the health of millions of Americans.” #InteropForum#Interoperability
@vijaypande Many thanks to @vijaypande for his inspiring and humbling words! We’re incredibly excited to be part of the @a16z portfolio, working on behalf of patients.
I do still question how can a patient ever get a second opinion or advocate for themselves if they can’t get access to their own medical record? 5-10 business days is utterly unacceptable if a patient needs urgent care.