Patient foundation advocates play a critical role in supporting the work of the Kids First Data Resource Center through advocacy and outreach efforts, promoting researcher enrollment, and informing others about the value of Kids First in driving progress toward more effective treatments and cures of childhood cancer and congenital conditions.
facebook
BlueskyLinkedIninstgramyoutubeFollow @kidsfirstdrc EMAIL KIDS FIRST Privacy Policy Cookies
The Kids First Data Resource Center (“DRC”) comprises partnered institutions supported by the NIH Common Fund under Award Number U2CHL138346 as part of the Common Fund’s Gabriella Miller Kids First Pediatric Research Program (“Kids First”). All content, terms and conditions and policies associated with the DRC Portal and Website (the “Services”) are produced by the DRC. The views and opinions of authors expressed on the Services do not necessarily state or reflect those of the National Institutes of Health (“NIH”) or the U.S. government. Furthermore, the NIH does not endorse or promote any DRC entity or any of its products or services nor guarantees the products, services, or information provided by the DRC.
© 2025 Gabriella Miller Kids First Data Resource Center. All rights reserved.
