Thrilled to work with Vijay Pande and the fantastic team at a16z! x.com/ciitizencorp/s…

"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

I just published “My Sister Tania” medium.com/p/my-sister-ta…

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 Nasha Fitter and Elli explain why we should all care! #rarediseaseday #WRDD2021 #ciitizen youtu.be/UPOfV5TWF6o

Memes are the only way to explain what we are building at Ciitizen... check out Nikhil Krishnan write up on us

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? hubs.li/H0HYXMr0 MBC Alliance

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 CBS News: cbsn.ws/3x9Y3ol"

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. blog.ciitizen.com/ciitizen-super…

🎉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!

Congratulations to Anil Sethi and the Ciitizen team — Invitae makes an amazing partner for the next stages of the mission.

@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!

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: bit.ly/3xMzNKp"

Proud of our work with @LLSUsa featured in the AACR report outlining the impact the COVID-19 #pandemic has had on #cancer #research and #patientcare. Dr. Saltzman, you inspire us all everyday!

If you remained at #PMWC18 this afternoon, wander over to Track 5 where we are excited to dialogue with members of @ciitizencorp on ways to collect, organize and share their data! #hcldr #hitsm

Just in case you need to help someone understand that it is YOUR RIGHT to access your own health data. Thanks to @healthprivacy @ciitizencorp #PMWC18 #ptexp

"The only way to solve this is to share data." - Tania Simoncelli regarding trying to provide clarity around VUS genetic results. We need mind share to validate benign and/or determine deleterious nature of results. #PMWC18 #genetics

"Data sharing is critical. It's hard." ~ Dr. Lincoln Nadauld of Intermountain Health Yep. This is why we need to allow patients to be stewards of their own data. Much more feasible (in my lifetime) than interoperability or silo busting. #PMWC18 #hcldr cc @ciitizencorp

Roses are red, violets are blue. #HIPAA says I can #getmyhealthdata, and you can get yours, too. #healthpolicyvalentines. Happy 💌 day Mark Savage

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.