Skip to main content
Hit enter to search or ESC to close
Close Search
search
Menu
Newsfeed
Shop
Resources
twitter
facebook
linkedin
youtube
instagram
tiktok
Patients
Understanding NF
NF1
NF2
-Related Schwannomatosis
Schwannomatosis
Find a Doctor
NF Registry
Resources
Patient Engagement
Clinical Trials
Healthcare Professionals
Diagnostic Criteria
Conferences & Education
Training Grants
Clinical Trials Pipeline
Researchers
Funding Opportunities
Conferences & Education
Research Tools & Resources
Pharma
For Pharma & Biotech
Industry Partnerships
Progress
Our Mission
Our Impact
About Us
Progress in NF1
Progress in
NF2
-Related Schwannomatosis
Progress in Schwannomatosis
Take Action
Make a Donation
Shine a Light on NF
NF Registry
Share Your Story
search
Donate
News
The latest news, stories, and updates from the Children's Tumor Foundation.
Search for:
Filter
Global
Featured
Featured EU
Global
NF2-SWN
Give for Hope: Rozalinda’s Challenges with NF2-SWN and Her Hope for Brigatinib
Rozalinda was just 21 years old when she received life-altering news that would reshape her…
Featured
Fundraiser
Global
Special Events
2024 National Gala Recap
On Monday, November 18, 2024, the NF patient community gathered with leading philanthropists, medical experts,…
Featured
Global
NF Conference
Press Release
Science & Research
Top Story EU
Children’s Tumor Foundation Europe Leads Collective Effort in Accelerating Therapeutics and Innovation for Rare Diseases
Gathering in Brussels for a week, a diverse group of leading experts from across the…
Featured EU
Global
Pharma
Nathalie Moll, Director General of EFPIA, Delivered the Opening Address at the Global NF Conference
"The community that looks after rare diseases, whether it’s scientists, patient communities, or industries, are…
Global
NF Conference
NF1
NF2-SWN
Press Release
Science & Research
SWN
Top Story
Top Story EU
Children’s Tumor Foundation Presents the 2024 Global NF Conference in Brussels: Shaping What’s Next for NF
(NEW YORK, NY and BRUSSELS, BELGIUM) - June 17, 2024 - The 2024 Global NF…
Collaborations & Partnerships
Featured
Featured EU
Global
NF1
Press Release
Healx to receive investment from Children’s Tumor Foundation to advance Neurofibromatosis Type 1 treatments
Milestone payments from CTF will support advance of Healx’s lead compound, HLX-1502, to clinical trials…
Featured
Featured EU
Global
Science & Research
Young Investigator: Q&A with Clara Nogué about schwannomatosis cell lines
The Young Investigator Award (YIA) provides two-year salary support to early-career NF researchers to help…
Global
NF1
Science & Research
Young Investigator: Q&A with Roope Kallionpää about NF1 and cancer risk
The Young Investigator Award (YIA) provides two-year salary support to early-career NF researchers to help…
Featured EU
Global
Press Release
Sabine Moravi Elevated to Vice Chair of CTF Europe Board of Directors
The Children’s Tumor Foundation (CTF) Europe is delighted to announce the elevation of Sabine Moravi…
Collaborations & Partnerships
Global
Rare Disease Day: Spotlighting NF Impact Through Goodwin
Today marks Rare Disease Day, a time when communities around the world come together to…
Featured EU
Global
Science & Research
CTF Europe is Hiring a CEO
Terrific opportunity for a European-based innovator ready to make an impact! Children's Tumor Foundation Europe…
Featured EU
Global
Press Release
Children’s Tumor Foundation Europe Welcomes Sabine Moravi to its Board of Directors
The Children’s Tumor Foundation (CTF) Europe, a leader in funding and driving research in Europe…
Close Menu
Donate
Patients
Understanding NF
NF1
NF2
-Related Schwannomatosis
Schwannomatosis
Find a Doctor
NF Registry
Resources
Patient Engagement
Clinical Trials
Healthcare Professionals
Diagnostic Criteria
Conferences & Education
Training Grants
Clinical Trials Pipeline
Researchers
Funding Opportunities
Conferences & Education
Research Tools & Resources
Pharma
For Pharma & Biotech
Industry Partnerships
Progress
Our Mission
Our Impact
About Us
Progress in NF1
Progress in
NF2
-Related Schwannomatosis
Progress in Schwannomatosis
Take Action
Make a Donation
Shine a Light on NF
NF Registry
Share Your Story
Newsfeed
Shop
Resources