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Childrens Tumor Foundation
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About
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Posts
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Story of NF: Michael M.
14 hours ago
in:
NF1
,
Story of NF
no comments
Children’s Tumor Foundation 2024 Impact Report
7 days ago
in:
Awareness
,
Top Story
,
Top Story EU
no comments
CTF CEO Annette Bakker Moderates Panel at World Orphan Drug Congress 2025
1 week ago
in:
Featured
,
Featured EU
,
Science & Research
no comments
How a Once-Abandoned Drug Found New Life – and Changed the Future for NF Patients
1 week ago
in:
CTF in the News
,
Featured
,
Featured EU
,
Science & Research
no comments
Story of NF: Lainey O.
2 weeks ago
in:
NF1
,
Story of NF
no comments
CTF-Hosted Lab Tour: Cincinnati Children’s Hospital
3 weeks ago
in:
Featured
,
Science & Research
no comments
Story of NF: Catherine K.
4 weeks ago
in:
NF1
,
Story of NF
no comments
Patient Day at the Global NF Conference
4 weeks ago
in:
Global
,
NF Conference
no comments
Young Investigator: Q&A with Sarah Morrow about NF1 and MPNST
1 month ago
in:
Awards & Grants
,
Featured
,
Featured EU
,
NF1
,
Science & Research
no comments
Children’s Tumor Foundation Chair Pens Message Urging Restoration of NF Research Funding
1 month ago
in:
Advocacy
,
Featured
,
Featured EU
no comments
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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
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Events & Fundraisers
Raise Awareness
Advocacy
Volunteer
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