Children's Tumor Foundation

foundation dedicated to improving the health and well-being of individuals and families affected by neurofibromatosis

The Children's Tumor Foundation (CTF) is a 501(c)(3) foundation that dedicate to improve the health and well-being of individuals and families affected by neurofibromatosis (NF). They have four-part mission includes propelling drug research and development through a series of strategic investments, strengthening patient support, increasing public awareness of NF and establishing best practices in clinical care for affected individuals.[1][2]

Children's Tumor Foundation
HeadquartersNew York City
Key peopleAnnette Bakker, PhD, President and Chief Scientific Officer
Linda H. Martin, Chair
Motto"Ending NF Through Research"
Vice President of Research and Development Salvatore La Rosa speaking at NIH Rare Disease Day in 2018

References

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  1. "Mission & Impact | Children's Tumor Foundation". www.ctf.org. Retrieved 2021-04-25.
  2. "Fight NF Your Way | Children's Tumor Foundation". www.ctf.org. Archived from the original on 2021-04-25. Retrieved 2021-04-25.