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Story of NF
NF1
Story of NF
Stories of NF: Katie P.
Awareness
NF2-SWN
Story of NF
Q&A: World-traveler and NF2 Hero Christina Tells Her Story
NF1
Story of NF
Stories of NF: Chloe M.
Story of NF
SWN
In My Own Words: Schwannomatosis at 27
NF1
Story of NF
Stories of NF: Blane H.
NF1
Story of NF
Stories of NF: Eddie P.
NF1
Story of NF
Stories of NF: Ryker S.
NF1
Story of NF
Stories of NF: Alexa D.
Special Events
Story of NF
Introducing the Inaugural Junior Board
NF1
Special Events
Story of NF
Meet Our 2020 NF Ambassador: Brianna Worden
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Story of NF: Lainey O.
CTF-Hosted Lab Tour: Cincinnati Children’s Hospital
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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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