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The latest news, stories, and updates from the Children's Tumor Foundation.
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NF1Story of NF
Story of NF: Michael M.
Michael was diagnosed with neurofibromatosis type 1 (NF1) at only two months old. NF has…
AwarenessTop StoryTop Story EU
Children’s Tumor Foundation 2024 Impact Report
The Children’s Tumor Foundation (CTF) has released its latest impact report, detailing significant progress in…
FeaturedFeatured EUScience & Research
CTF CEO Annette Bakker Moderates Panel at World Orphan Drug Congress 2025
Children’s Tumor Foundation CEO Annette Bakker to speak on unleashing the life-changing potential of shelved…
CTF in the NewsFeaturedFeatured EUScience & Research
How a Once-Abandoned Drug Found New Life – and Changed the Future for NF Patients
The drug mirdametinib was once shelved by Pfizer. Today, it’s Gomekli - an FDA-approved treatment…
NF1Story of NF
Story of NF: Lainey O.
This Story of NF was submitted by Lainey's mother, Whitney. It all happened very suddenly…
FeaturedScience & Research
CTF-Hosted Lab Tour: Cincinnati Children’s Hospital
The Children’s Tumor Foundation was proud to host a group of patients and families affected…
NF1Story of NF
Story of NF: Catherine K.
When I was born, something wasn’t right with my eyes. One was basically closed shut;…
GlobalNF Conference
Patient Day at the Global NF Conference
As part of the 2024 Global NF Conference, the Children’s Tumor Foundation hosted its second…
Awards & GrantsFeaturedFeatured EUNF1Science & Research
Young Investigator: Q&A with Sarah Morrow about NF1 and MPNST
The Young Investigator Award (YIA) provides two-year salary support to early-career NF researchers to help…
AdvocacyFeaturedFeatured EU
Children’s Tumor Foundation Chair Pens Message Urging Restoration of NF Research Funding
In an op-ed published in RealClearHealth, Gabriel Groisman, Chair of the Children's Tumor Foundation, calls…
AdvocacyFeatured
Standing Strong for NF Research and How You Can Help
March 26, 2025 Update: Dear Friends, I’m reaching out about the federal NF research funding…
NF2-SWNStory of NF
Story of NF: Anisha R.
I was diagnosed at the age of 26 in 2022. I experienced extraordinary NF2-SWN effects…