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Understanding NF
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-Related Schwannomatosis
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Awareness
Awareness
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Washington Nationals’ Shortstop Ian Desmond Helps Fight NF!
Awareness
NF Endurance
Ways to Give
We’re All on the Same Team When It Comes to Ending NF
Awareness
CTF Supports Rare Disease Day
Awareness
Publications
Reflections on My First Two Years at the Children’s Tumor Foundation
Awareness
Tribute to Children’s Tumor Foundation Board Member Harold Ramis
Awareness
Ways to Give
Cupid’s Undie Run on National Television!
Awareness
Ways to Give
Biggest Rolex 24 Fundraising Campaign Ever for CTF/R4R at Daytona
Awareness
Children’s Tumor Foundation Announces Leadership Change
Awareness
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Racing4Research Makes Colorful Return to Daytona with Park Place
Awareness
Video
Children’s Tumor Foundation Has a New Logo!
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Recent Posts
Story of NF: Lainey O.
CTF-Hosted Lab Tour: Cincinnati Children’s Hospital
Story of NF: Catherine K.
Patient Day at the Global NF Conference
Young Investigator: Q&A with Sarah Morrow about NF1 and MPNST
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Patients
Understanding NF
Neurofibromatosis Type 1
NF2
-Related Schwannomatosis
Schwannomatosis
Find a Doctor
NF Treatments
NF Registry
Resource Center
Educational Events
Patient Engagement
Clinical Trials
Healthcare Professionals
Diagnostic Criteria
NF Clinic Network (NFCN)
Conferences & Education
Partnerships
Clinical Trials Pipeline
Researchers
Funding Opportunities
Conferences & Education
Research Tools & Resources
Leading Minds in NF Research
Pharma
For Pharma & Biotech
Industry Partnerships
Progress
Our Mission
Our Impact
About CTF
Progress in Neurofibromatosis Type 1
Progress in
NF2
Related Schwannomatosis
Progress in Schwannomatosis
Take Action
Ways to Give
Events & Fundraisers
Raise Awareness
Advocacy
Volunteer
Share Your Story
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