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Please join us now by making a gift. We refuse to lose any momentum in our fight against NF!
Give TodayWhat is NF? NF refers to a group of genetic conditions that cause tumors to grow on nerves throughout the body. NF includes neurofibromatosis type 1 (NF1) and all types of schwannomatosis (SWN), including NF2-related schwannomatosis (NF2-SWN), formerly known as neurofibromatosis type 2, or NF2. NF affects 4 million people worldwide. Anyone can be born with NF, and it impacts everyone differently.
Everything we do is to bring treatments to patients as we work toward a cure.
Meet a courageous mom whose journey with her daughter’s NF diagnosis began with uncertainty—but led to hope through the Children’s Tumor Foundation (CTF). Kimberly Snipes shares how CTF became a lifeline, offering answers, support, and a community that understands. Watch her story, and discover how CTF can be a source of strength and guidance for you, too.
By connecting patients, doctors, scientists, and pharma, we drive treatments, advance care, and deliver results for millions affected by neurofibromatosis or schwannomatosis.
More than 20,000 patients a year visit our NF Clinic Network, which includes more than 70 clinics across North America.
We connect patients with the education and information they need through patient brochures and educational webinars.
Join the thousands who have enrolled in the NF Registry, a critical tool in matching NF patients to clinical trials.
CTF drives vital research, scientific collaborations, and partnerships that accelerate NF research and drug development.
Everything we do is to bring treatments to patients as we work toward a cure.
Our ongoing partnerships with pharmaceutical and biotech companies catalyze treatments for NF.
Shine a Light NF Walk program brings local families and friends together to raise funds, promote awareness, and build community.
Professional and amateur athletes run, bike, and swim in endurance events to raise awareness and funds for NF research.
CTF hosts events all over the country both in-person and virtual for patients, families, clinicians, specialists, and researchers.
Search our website for news and information about NF.
Join our mailing list for news, exclusive resources, events and opportunities.
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