Sharing from our friends at the National Down Syndrome Society. We believe that no child should be discriminated against in their fight...

#GivingTuesday #Transplant Today’s Giving Tuesday! There are endless ways to express your radical generosity. Here are 5 of ours! How do...

Join CareDx and Transplant Families for this informative discussion on the importance of advocacy and open communication with your...

Transplant Families and the @AmericanSocietyofTransplantation are pleased to present an update on COVID-19 and pediatric transplantation....

JOIN US THIS THURSDAY, SEPTEMBER 9TH AT 4 PM PST/7 PM EST Transplant Families is honored to host Analy Navarro as she reads from her...

For the complete updated document please go to the PIDS website. ACTION Learning Network has brought us easily distributable infographics...

The Stanford Children's Health Liver Care Center and Liver Transplant Program is presenting a patient webinar on biliary atresia from...

School lunches for transplant kids can be very different than for their peers. Transplant kids have certain dietary restrictions that are...

We at Transplant Families are always happy to find organizations like Give InKind that truly make our community better. Hospital life is...

Please join CareDx, Starzl Network for Excellence in Pediatric Transplantation, and Transplant Families, for this live interactive...

May 2021 Newsletter 🌱 - available now! Conference video links, congrats to our grads, thank you to our transplant nurses, mental health...

Pediatric Transplant Conference 2021 Videos now available in our library and on YouTube.

**Editor's note: We are privileged to be able to bring you Board Member Jill Brown and her daughter Kylee's story this month. Jill is a...

A conference for the pediatric transplant community that will mark the end of National Pediatric Transplant Week. We hope you will be...

Transplant Families February Newsletter (mailchi.mp)

We were so happy to catch up with the Buskirk family recently. When they were last interviewed, they had been through so much with their...

In honor of #RareDiseaseDay, we salute all the parent caregivers that support these amazing kids. We also have a call to action to...

Join us for the Move Every Mountain Hike-a-thon. This campaign is one that celebrates being active anytime after receiving your gift of...

There is so much going on already this year. We hope that you will take a look at the latest newsletter for community updates and events....

It was six years ago in January that Caylyn and Chris, as well as the world, welcomed the small miracle of Oliver. Oliver is unique...