So so proud of my roommate @j_richards27 and the amazing @thelukewhiting on publicly announcing Evergrow, whose mission is to ensure our future on Earth by enabling and accelerating every project that reduces humanity’s carbon footprint.
https://t.co/GoAP2R30IE
I am so proud of the @_allstripes team and our community. Big milestone - we've raised $50m in new capital to continue our mission to unlock new treatments for people affected by rare disease. Onwards! #RareDisease#Funding
Excited to have @_allstripes’s CEO @nancyyu25 on the next Gene Fixers this Thursday, Mar 4 at 2:00 PM PST on @joinclubhouse.
We’ll discuss how patient data is powering clinical insights and turbocharging genetic disease research.
Join us! https://t.co/EZfPYFUNZD
Happy rare disease day! @_allstripes collaborates with Sheryl Sandberg and Adam Grant’s @optionb and our patient ambassador community to raise awareness in the rare disease community. 💪 https://t.co/n10Ri2wxVm
It’s #RareDiseaseDay! The experience of every person affected by rare disease matters, and here at AllStripes we’re honored to partner with patients and caregivers to unlock new treatments. Who are you fighting for this Rare Disease Day? #RareDiseaseDay2021#ShowYourStripes
I find this thesis fascinating.
Would love to hear what both traditional VCs and project finance investors think of it.
What would a fund need to do structurally to be able to capture the upside from both?
https://t.co/9L6UVwIbwy
We are excited to announce our partnership with the Orphan Disease Center and @PennMedicine to advance clinical understanding of #rarediseases. Read more through this press release: https://t.co/jy1BovFcaP
This is a story that Judge Jeffrey Sutton shares about an encounter late in my dad's life, when he bought his friend Ruth two dozen roses for her birthday. "Some things in life are more important than votes."
AllStripes works with patient foundations to complement their registry efforts with data insights that can jumpstart new research. Thank you for your partnership! #rarediseases
It’s official, RDMD has a new name: AllStripes Research! The zebra is the global symbol for the rare disease community – AllStripes represents the collective strength of patients and families coming together to drive forward treatments. Visit https://t.co/fVaBxpScBu! #raredisease
The zebra has long been a symbol for all the rare disease warriors out there, so to us, AllStripes represents the collective strength of patients coming together to drive forward and unlock new treatments.
“When you hear hoofbeats...”
We started RDMD two years ago to unlock new treatments for people with rare disease. Throughout my time as a researcher and at 23andMe, I've found it fascinating that patients and drug researchers are often on the same side of the table seeking new treatments,
Today we've renamed RDMD to AllStripes. We love this new look because we're committed to unlocking new treatments for all 7,000 rare disease communities.