Clarity. Connection. Hope.

Facing a neuroendocrine tumor (NET) diagnosis can feel overwhelming. At FLaNET, we make sure no patient or caregiver has to go through it alone.

Connected Care

FLaNET: Neuroendocrine Cancer Community

We are a patient-led nonprofit dedicated to helping people with NETs and their loved ones navigate diagnosis, treatment, and beyond. Founded by patients, caregivers, and clinicians, we bridge the gap between complex medical information and the real-world questions families face every day.

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NETs Are Rare — But You’re Not Alone

While only about 4,000 people in the U.S. are diagnosed with a NET each year, more than 175,000 are living with this disease. Together, we form a strong community of patients, caregivers, and advocates who understand what you’re facing.
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NETs Can Affect Anyone

NETs don’t discriminate—they can develop in children, adults, or older adults, with most diagnoses occurring between ages 50 and 60. Whatever your age or stage, support and expert care are here for you and your loved ones.
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Early Detection Brings Hope

Finding NETs sooner means better outcomes. That’s why we work to unite patients, caregivers, and physicians—sharing education, resources, and support to make early diagnosis and treatment possible.

Why FLaNET

Patient-First

Everything we do is designed for those living with NETs.

Clear &
Compassionate

We translate medical complexity into simple, supportive guidance.

Connected Care

We bring patients, families, physicians, and partners together for stronger outcomes.

Trusted Experts

Backed by clinicians, advocates, and lived experience.

Stories That Heal

Through videos, articles, and events, we highlight real patient journeys of resilience and hope—because no one should face NETs in silence.

Get Involved

Your support helps drive awareness, education, and connection for NET patients across Florida and beyond.