When Maria is asked why she has to go to the doctor so much, she needs a little help. Children's Tumor Foundation mascots Moxie and Sparx come to the rescue! They help Maria explain neurofibromatosis type 1, also called NF1 . . . but maybe Maria knows more about NF than she thought!
You can read & freely download our short comic book by the same name at:
www.ctf.org/images/uploads/resources/Moxie_and_Sparx_Explain_NF1.pdf
More CTF resources about NF can be found at:
www.ctf.org/understanding-nf/tools-for-kids
What is the Children's Tumor Foundation?
Children’s Tumor Foundation (CTF) began as the first grassroots organization solely dedicated to finding treatments for NF. Today, CTF is a highly recognized global nonprofit foundation, the leading force in the fight to end NF, and a model for other innovative research endeavors.
Visit our website at www.ctf.org/
Donate today at www.ctf.org/ways-to-give/
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Facebook - childrenstumor
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LinkedIn - www.linkedin.com/company/children's-tumor-foundation
#endnf #nf1 #nf2 #nf2swn #swn #childrenstumor #neurofibromatosis #schwannomatosis #nervetumor #tumor