Hello [[INITIATIVE.AUDIENCE MEMBER.FIRST NAME]], 

I am so excited to share about one of our newest partnerships. Our collaboration with CanCare allows us to provide free, one-on-one emotional support to liver cancer patients and caregivers.

A liver cancer diagnosis does not just affect the person in the exam room. It impacts spouses, children, parents, siblings, and friends. Fear, confusion, and isolation often appear long before answers do. Through our partnership with CanCare, Blue Faery can connect individuals with trained and compassionate support volunteers who understand what it means to face cancer, not just clinically, but emotionally.

This one-on-one support is confidential, personalized, and available at no cost. Sometimes what people need most is not another pamphlet or statistic, but a real conversation with someone who truly listens.

While support is critical year-round, February also gives us an opportunity to focus on Black History Month and liver health. Black and African American communities face higher risks for liver disease and liver cancer, yet too often receive information too late or not at all. Earlier this month, we hosted our Love Your Liver Black History Month workshop to address these disparities directly. If you were not able to attend live, I strongly encourage you to watch the replay and share it with someone who might benefit. Knowledge truly can save lives.

Looking ahead, we are also preparing to launch our next The Truth About Liver Cancer workshop series in March, beginning with HCC and the Family Impact. Liver cancer does not happen in isolation. This session will explore how a diagnosis affects the entire family emotionally, practically, and financially, and will offer guidance and resources to help families navigate what comes next.

Everything we do at Blue Faery comes back to one simple belief: no one should face liver cancer alone. That is why we provide trusted information, meaningful support, and a strong community. Whether through education, advocacy, or one-on-one connection, we are here, and we are grateful you are too.

Thank you for standing with us.

Fighting Liver Cancer Together,
Andrea Wilson Woods
Founder and President 

We would love to hear how Blue Faery has made a difference in your life. Your story can inspire patients, caregivers, and advocates across our community, and sharing it is simple. When you open the link, please click the volume icon to hear Andrea's message before clicking the record button.

Join us on March 7, 2026 for the first The Truth About Liver Cancer workshop of 2026, featuring real life perspectives from two families who have navigated a liver cancer diagnosis. Through their stories, attendees will gain meaningful insight into caregiving, communication, coping, and family resilience.

A liver cancer diagnosis affects more than just the patient. It impacts the entire family. This webinar focuses on the emotional, practical, and relational challenges families face when someone is diagnosed with hepatocellular carcinoma.

💙Coming Soon: Houston HCC Lunch & Learn💙

We're bringing our HCC Lunch & Learn to Houston in April! While details are still coming together, we wanted you to be the first to know something special is on the way. In the meantime, take a look at the sizzle reel from last year's HCC Lunch & Learn to get a feel for the energy, the education, and the powerful conversations that happen when our community comes together.

Are you interested in sharing your experiences with Liver Cancer with others?

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 best to design a clinical trial that addresses the unique needs of individuals with this condition.

The virtual focus group would take place in February 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 to eligible participants.

If you are interested in participating in this opportunity or have any additional questions, please contact:
Lola Hill
Phone: 617-725-2750 ext. 427 
Email: lhill@ciscrp.org

*Indicates a paid listing. If your trial is no longer recruiting, please email Chasity right away.