Heading to Washington, DC 🇺🇸 with the @AmericanLiverFdtn to advocate for liver health, transplant access, donor protections & disease prevention.
Proud to represent Georgia for the 2nd year in a row on bills that save lives and reduce long‑term healthcare costs.
#LiverHealth
National #DonateLifeMonth starts in April! Here is a calendar with key dates and ways you can join all month 💙💚 Check out https://t.co/cPn8kOsh0Z for more info & resources! ✨
🚨 URGENT PLEA FOR A LIVING DONOR - CLICK BELOW FOR INFORMATION AND PLEASE SHARE THIS STORY! 🚨
South Georgia Family Seeks Living Donor As Son Endures Nightly Peritoneal Dialysis
Visit our #GiftOfLife category for to help many more in need of living ...
https://t.co/drxtdMCoaO
Proud to be this year’s #LiverLife Walk Chair 💚
100+ liver diseases. Awareness matters.
$5 = impact
Join my 50 Warriors & support liver health ⬇️
https://t.co/e5h1WY8IMg
I hope this will be allowed. The Liver Circle will be hosting a zoom with the chair of the host committee, Transplant Games of America tomorrow at 11 am. This is your chance to ask all things Transplant Games, the link is on our website.💙💚
https://t.co/j6PqturLcP
The Center for Information and Study on Clinical Research Participation (CISCRP), together with a pharmaceutical company, is planning a virtual focus group with adults diagnosed with metastatic hepatocellular carcinoma (mHCC) and/or their care partners to discuss their experiences, share general thoughts on clinical research, and provide feedback on a proposed clinical study evaluating a new treatment for mHCC.
The goal of the focus group is not to recruit for a clinical trial, but rather to learn from patients and care partners how to best create a clinical trial that addresses the unique needs of individuals with this condition.
The virtual focus group would take place in March 2026, with the exact date and time to be determined based on participant availability. The focus group will be conducted virtually using an online platform (Zoom) as a single 2-hour meeting.
As a thank you for your time, CISCRP will provide an honorarium for those who are eligible and participate.
If you are interested in participating in this opportunity or have any additional questions, please visit: https://t.co/uwAIcI2SMk to fill out your form and we’ll get back to you shortly.
ALF’s Health Policy Round-Up is here, and there’s breaking news on the Living Donor Protection Act (LDPA).
We’re also tracking major public health leadership updates that could shape what’s next.
Get the full update: https://t.co/ZSnqbbnarZ
#HealthPolicy#LivingDonation #LiverAdvocacy #PublicHealth
#TransplantEquity
Today, American Liver Foundation is proud to announce a new partnership with @heliogenomics that empowers millions of Americans to find out if they are at risk for, or already have, liver cancer. #Livercancer is rapidly becoming a public health crisis and is often called a “silent killer” because most people have no symptoms in the early stages.
“Our goal through this partnership is to provide advanced tools so that we have an educated, informed public which understands their liver cancer status before it’s too late,” said Lorraine Stiehl, CEO of American Liver Foundation.''
Read more about how this partnership is advancing early detection and saving lives: https://t.co/s8OQtP3bS4
#LiverCancerAwareness #EarlyDetectionSavesLives #LiverHealth #CancerPrevention #ThinkLiverThinkLife
Hi, X👋It's been a minute. I'm back with something meaningful to share. I've been named Chair for the 2026 Atlanta Liver Life Walk- and I'm ready to raise awareness + hope. 💚
Liver disease affects approximately 100 million Americans. An estimated 80-100 million people in the US have some form of fatty liver disease (now called steatotic liver disease).
I’m going to Washington, DC April 29th and 30th! I’ll be joining @American Liver Foundation for the 2025 Liver Life Advocacy Summit. to be on Capitol Hill to advocate for the 100 million Americans affected by liver disease.
On my way to Washington, DC!