CNCF Hope Children's Neuroblastoma Cancer Foundation

06/24/2026

The countdown is on!

The 2026 CNCF Parent & Caregiver Education Conference is just one month away, and we can't wait to bring families together for a weekend of learning, connection, and hope.

💛 Hear directly from leading neuroblastoma experts
💛 Connect with families who truly understand
💛 Gain knowledge, resources, and support for wherever you are on the journey

July 24–25, 2026
Chicago Marriott Oak Brook

Travel assistance is available. Please contact Nicci at [email protected] for more information.

We hope to see you there!

🔗 https://fundraise.givesmart.com/e/yqxTvw

06/23/2026

💛 Supporting Families. Funding Research. Building Hope.

Every donation helps CNCF provide education, support families, and advance neuroblastoma research.

Together, we can do more.

www.cncfhope.org

06/22/2026

A neuroblastoma diagnosis changes a family forever.

The questions. The decisions. The uncertainty.

That's why CNCF is here—to help families find trusted information, meaningful support, and a community that understands the journey.

The CNCF Parent & Caregiver Education Conference is at the heart of that mission, bringing families together with leading neuroblastoma experts, survivors, and other families who truly understand. Because knowledge brings clarity. And clarity brings hope.

Together, we are stronger than neuroblastoma.

www.cncfhope.org

06/19/2026

Have you registered yet for the 2026 CNCF Parent & Caregiver Education Conference? 💛

Join families from across the country for a weekend of education, connection, support, and hope. Hear from neuroblastoma experts, connect with other families who understand the journey, and gain valuable information and resources.

📅 July 24–25, 2026
📍 Chicago Marriott Oak Brook

Travel assistance is available. Please contact Nicci at [email protected] for more information.

Register today:
https://fundraise.givesmart.com/e/yqxTvw?vid=1oio19

06/18/2026

Most people have never heard the word neuroblastoma.

But for hundreds of families each year, it's a word that changes everything.

Neuroblastoma is a rare childhood cancer that most often affects babies and young children. It develops in the nervous system and can be difficult to detect in its earliest stages.

💛 About 750 children in the U.S. are diagnosed each year
💛 Most children are diagnosed before the age of 5
💛 More awareness can lead to more support, research, and hope

The first step is simply knowing the word.

Neuroblastoma.
Say it. Know it. Defeat it.

06/17/2026

No family should face neuroblastoma alone.

CNCF is more than an organization—it's a community of families, survivors, researchers, healthcare professionals, and supporters working together to make a difference.

Thank you for helping us bring hope, support, and resources to families when they need it most.

Hope Unites Us.

To learn more, go to www.cncfhope.org

06/16/2026

Neuroblastoma may be rare, but the need for research, support, and education is not.

Every donation to CNCF helps fund programs and resources that bring hope to children and families facing neuroblastoma.

If CNCF has touched your family, helped you learn, connected you with others, or given you hope, please consider supporting our mission.

Together, we can do more.

Donte Today: https://www.cncfhope.org/donate/

💛 Hope Unites Us.

06/15/2026

🌽 Every bag tossed helps bring hope. 💛

The Shuck You Cancer Co****le Tournament is more than just a night of friendly competition — it's an opportunity to come together as a community and support children and families affected by neuroblastoma.

Whether you're aiming for the championship or just looking for a fun night out with friends, your participation helps CNCF continue funding research, education, awareness, and support programs for families facing this disease.

📅 Friday, July 17, 2026
📍 West Dundee, IL
💲 $60 per team

Grab a partner and join us for a night of fun, connection, and making a difference.

Register today:
https://fundraise.givesmart.com/e/BhQwJg?vid=1oowg5

****leTournament

06/12/2026

Join families from across the country for a weekend of education, connection, support, and hope.

Email from Children's Neuroblastoma Cancer Foundation   Hello CNCF Families, We hope you're doing well. As someone who has attended a CNCF Parent & Caregiver Education Conference in the past, you know

06/11/2026

When symptoms don't add up, testing can provide answers.

Because neuroblastoma symptoms are often vague and can look like everyday childhood illnesses, doctors rely on several tests to make a diagnosis:

🔹 MRI, CT, and MIBG scans
🔹 Blood and urine testing
🔹 Tumor biopsy
🔹 Bone marrow evaluation

Early and accurate diagnosis is an important step toward treatment and care.

💛 Neuroblastoma: Say it. Know it. Defeat it.

Learn more: www.cncfhope.org