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Monthly Archives
August 2018
This Is NF
This is NF: Marisa McGrody
Newsletter
Leading the Way: Children’s Tumor Foundation Annual Report
This Is NF
This is NF: Matt Hay
This Is NF
This is NF: Susan Giza
This Is NF
This is NF: Tom LaGuidice
CTF in the News
NF1
Publications
Science & Research
‘Pig Models’ Advance the Study and Treatment of NF1
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Recent Posts
Children’s Tumor Foundation 2024 Impact Report
CTF CEO Annette Bakker Moderates Panel at World Orphan Drug Congress 2025
How a Once-Abandoned Drug Found New Life – and Changed the Future for NF Patients
Story of NF: Lainey O.
CTF-Hosted Lab Tour: Cincinnati Children’s Hospital
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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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